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<h3>Job Description</h3>
Job Description
Do you want to be part of our flourishing expansion across the US?
Founded in 1977, Planteria has evolved from a small startup into the UK largest interior landscaping company it is today, with an impressive annual turnover of £20 million. With a focus on strategic partnerships, continuous innovation and client satisfaction, the company has accelerated its growth in the past 3 years and achieved a 33% year-on-year growth over this period, and now employs over 180 staff.
Following our recent success in New York we are now looking for Interior Horticultural Technicians to join our growing team in the Los Angeles area on a part time basis 24 hours per week (3 days). 
This role focuses on looking after our plants in client offices in Los Angeles. Our technicians provide excellent customer service and are knowledgeable about the maintenance and care of office plants. This is an independent role which involves early starts each day, taking ownership for plant maintenance at several client sites, on a weekly rota. Technicians are part of a team of like-minded plant specialists who meet regularly both online and in person. 
<ul>
<li>Maintain to a high standard internal plant displays at a number of client sites every day</li>
<li>Provide excellent customer service, including completing site reports and maintaining accurate data in our company systems</li>
<li>Work with your line manager and scheduler to ensure all rounds are completed efficiently and accurately</li>
<li>Work safely and in line with all risk assessments and method statements</li>
</ul>
Requirements
<ul>
<li>Excellent communication skills</li>
<li>Excellent customer service skills</li>
<li>Good problem solver </li>
<li>A passion for plants</li>
<li>Able to navigate the city using the Subway and bus links</li>
<li>Comfortable working independently but able to share knowledge and information with the wider team</li>
<li>Able to orient yourself in large office buildings</li>
<li>Some specialist horticultural knowledge (but full training will be provided)</li>
<li>Physically able to use watering cans, stepladders, and stools as part of the daily job </li>
<li>Experience working in a service industry</li>
<li>Experience working across multiple sites is desirable</li>
<li>Experience in planting or horticulture is desirable</li>
<li>Full clean driving licence is desirable as there may be some travelling between sites</li>
</ul>
<ul>
<li>Role is based at client sites so you will need to have access to good public transport links and have a full driving license </li>
<li>The role will also require a 2 week training period in San Franisco </li>
</ul>
Salary for this role is $48,000-$52,000 Full time equivalent. Part time hours of 24 hours per week is a $28,000-$31,000 annual salary. 
Benefits
<ul>
<li>A great salary package</li>
<li>Ongoing training and development</li>
<li>Uniform</li>
</ul>

Horticultural Technician ( Part time)

<h3>Job Description</h3>
Job DescriptionAbout The Role
We are seeking a highly effective, motivated recent graduate to join our team. You will experience all facets of building a startup at a cutting edge biotech company in San Carlos! You will work with an experienced team of founders and scientists running lab experiments and assays. You are a good fit for this role if you resonate with our values: namely if you work hard, are ambitious, creative, and honest, write python scripts to solve your problems, and will do whatever it takes to win.
Application Requirements:
Your cover letter should be one page give clear examples of the following:
<ul>
<li>An instance in which you demonstrated an exceptional work ethic</li>
<li>An instance in which you unblocked the critical path</li>
<li>An instance in which you demonstrated exceptional attention to detail</li>
</ul>
This job is not 9-5
<ul>
<li>This is an opportunity to work very hard, learn a lot, and develop skills that will serve you well later in life</li>
<li>This is not an opportunity to focus on work life balance</li>
</ul>
Who You Are:
<ul>
<li>BS in STEM or biology field with GPA &gt;= 3.5 and &lt;=1 year out of undergrad</li>
<li>Extremely strong work ethic</li>
<li>Python scripting ability</li>
<li>Highly motivated and ambitious</li>
<li>Proficiency with Google Sheets and Google Slides</li>
<li>Live within a 30 minute commute of San Carlos</li>
<li>Knowledge of aseptic technique OR experience with cell culturing OR experience working in a biosafety cabinet</li>
</ul>
Nice to Haves:
<ul>
<li>Experience with reporter cell assays</li>
<li>Knowledge of USP guidelines</li>
<li>Experience working with an HPLC</li>
<li>Experience working with a plate reader</li>
<li>Experience with qPCR</li>
</ul>
Key Responsibilities:
Under the guidance of a research scientist, perform lab work including:
<ul>
<li>Expression of biologics in mammal cells</li>
<li>Quality control of sterile compounded pharmaceuticals</li>
<li>Characterization of biologics using reporter cell lines</li>
</ul>
Additionally:
<ul>
<li>Record experimental methods and results in Benchling</li>
<li>Read and summarize papers</li>
<li>Contribute to BD efforts</li>
<li>Whatever else is needed for the company to succeed</li>
</ul>
Other Responsibilities
This job description is not intended to be all-inclusive. From time to time you may be required to perform other related duties as assigned to meet operational needs.
Details:
<ul>
<li>This is an in-person role in San Carlos, CA</li>
<li>The compensation range for this role is $100,000-110,000 along with equity options in the company and benefits</li>
</ul>
Life at Bioworks: Where Science Meets Culture
<ul>
<li>Comprehensive Health Coverage – Medical, dental, and vision insurance to keep you at your best</li>
<li>Financial Security – 401(k) with company matching and fully covered life insurance</li>
<li>Time to Recharge – Unlimited PTO, generous company holidays, and flexibility to take the time you need</li>
<li>Connection &amp; Community – Team lunches, office hangouts, and offsite meetups to build meaningful relationships</li>
<li>High-Impact Work – Shape the future of healthcare at a pivotal moment in our growth</li>
<li>Competitive Compensation – Top-tier salary and a generous equity package</li>
<li>Fast-Paced &amp; Exciting – Join a hypergrowth team that moves fast and builds with purpose</li>
<li>World-Class Team – Work alongside top researchers, scientists, and engineers in a high-performance environment</li>
</ul>
Equal Opportunity Employer
We are proud to be an equal opportunity workplace who prohibits discrimination and harassment of any kind. We celebrate diversity and are committed to creating an inclusive environment for all employees regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability or veteran status. We provide a work environment free of discrimination and harassment. All employment decisions are based on business needs, job requirements, and individual qualifications without regard to race, color, religion, sex, gender identity or expression, sexual orientation, national origin, disability status, protected veteran status, or any other protected characteristic as outlined by federal, state, or local laws.
We welcome all with a drive to work, and a curiosity to learn. We are here to build and be a part of science encompassing the full power and possibility for breakthrough innovation! 
To view our current job openings and apply, please visit our job portal. If you think you have what it takes but don't see a job fitting your skillset email us at <a href="mailto:recruiting@aequitabioworks.com" target="_blank">recruiting@aequitabioworks.com</a>.

Research Associate

<h3>Job Description</h3>
Job DescriptionDescription:
Aragen Bioscience is a leading contract research organization focused on accelerating product development. Aragen’s offerings include an entire portfolio of preclinical research services including cell-based assays and in vivo models of disease. We offer clients high quality service and superior R&amp;D partnerships.
 
Position Overview:
Research Associates / Senior Research Associates will be responsible for primarily conducting in vivo experiments to evaluate efficacy of client test compounds across various rodent models with a secondary role in supporting in vitro/ex vivo lab work and aiding in staff distributed duties to support daily lab and vivarium operations. A successful candidate will have hands-on experience with in vivo animal studies and working knowledge of in vitro laboratory techniques to support in vivo studies, such as tissue culture, RNA/DNA processing, and ELISA/Western Blot. Candidates will work closely with multidisciplinary teams to support various client and internal projects.
Key Responsibilities:
-Assist in the design and execution of in vivo rodent studies across various therapeutic areas with duties including animal weighing, dose administration (e.g. subQ, IP, PO, IM, retro-orbital, IV), blood and tissue collection, necropsy, oncology and functional readouts.
-Perform in vivo imaging and analysis of data in cancer models
-Proficient with cell culture techniques using various immortalized cell lines to support oncology studies is desired
-General understanding of pharmacokinetics, pharmacodynamics, and drug metabolism
-Ability to follow strict instructions on formulation of test compounds for in vivo dosing
-Analyze in vivo data independently or under minimal guidance of senior scientists
-Contribute to generation of reports for in vivo experiments or other related study presentations with guidance of senior scientists
-Work collaboratively with cross-functional teams to support department’s goals and timelines
-Aid in lab equipment maintenance and general lab support 
-Maintain a safe laboratory environment by following standard operating procedures (SOP) and established IACUC protocols
-Other related duties as assigned
 
Requirements:
Required Qualifications:
-BA/BS or MS in Biology, Immunology, Biomedical Sciences, Microbiology, Virology, Pharmaceutical Sciences, Pharmacology or a related discipline
-Two or more years of laboratory experience utilizing techniques or methods required by the position or an equivalent combination of education and experience in an academic lab environment
-Recent post graduates with a desire to expand their skill set are encouraged to apply
-Must be comfortable working with rodents and animal derived tissues or fluids 
-Adept at using automated instrumentation for analysis (e.g. IDEXX or HESKA machines)
-Openness to learning new methods and skills for shifting research needs based on clients
-General understanding of data analysis techniques and use of software (e.g. Microsoft Excel and Graph Pad Prism)
-Excellent organizational skills with attention to detail and ability to prioritize tasks to meet deadlines
-Strong written/verbal communication skills for assisting with writing reports, presentations, and client interactions
-Some evening and weekend/holiday hours are required 
Extensive and relevant research experience using rodent models of human disease 
-Proficiency in a specialized therapeutic area such as fibrosis, virology, autoimmune disorders, immunology, and oncology 
-Experience with oncology models
-Experience with in vitro/ex vivo assay development
-Hands-on knowledge of general laboratory techniques, including basic molecular or cellular biology techniques (e.g. RNA/DNA isolation, gel electrophoresis, PCR, RNASeq, bacterial culture and transformation, Western Blot, ELISA, mammalian cell culture, etc.)
-Working familiarity with cell based immunology techniques such as MSD/ELISA and FACS
-Understanding of preclinical drug development and regulatory process
-Prior experience handling small molecules/biologics for PK/PD studies
No Sponsorship will be offered. Seeking local candidates
Why Join Us?
Aragen Bioscience provides a stimulating work environment in which talented employees expand their technical skills and scientific knowledge and contribute directly to the ongoing success of the organization. The Company is located in Morgan Hill, California, at the south end of the Silicon Valley. We offer excellent salary and benefits. Aragen is an equal opportunity employer.

Research Associate/Sr Research Associate: In vivo Preclinical Research

<h3>Job Description</h3>
Job DescriptionBioPhase partners with the best Biotech, Pharmaceutical, and Medical Device companies in San Diego, and is in need of Recent Grads and Research Associates in the following disciplines- Molecular BiologyCell BiologyBioChemistryChemistryGeneral BiologyMicrobiologyAll related Scientific Disciplines Salary Range - $60k - $95k per year WILL TRAIN. Duties include both cutting edge Research activities and exciting opportunities in Biotech Manufacturing. For confidentiality reasons, additional information to be provided upon request. Multiple upper level positions also open for those candidates with BS Degrees in the above or related areas with 0-2 years of experience. Please feel free to apply and send your resume ASAP for details. #Zip

Attn: Research Associates & Recent Grads

<h3>Job Description</h3>
Job DescriptionMolecular Matrix is pioneering innovative medical devices for tissue regeneration applications in multiple organ systems. We are seeking highly motivated, self-sufficient candidates who are interested in growing with our company in a fast-paced and exciting environment. About the role: Reporting to the Research &amp; Development Lead, the Research Associate will use cell culture and molecular biology techniques to support the development of tissue engineering medical devices. The Research Associate works primarily in R&amp;D to support advancements in bioprocessing, scaffolding, and large-scale tissue formation. About You: You are an experienced Bachelor's or Master's level cell biologist and/or molecular biologist who enjoys collaborating across disciplines in order to solve complex problems. You are good at communicating ideas, data, and bottle-necks to technical and non-technical audiences alike. You have knowledge or interest in tissue engineering and medical devices and are excited to bring your experience and enthusiasm to this nascent industry. You thrive in fast-paced environments. Responsibilities: 
<ul>
<li>Perform molecular cloning: PCR, restriction digest, DNA assembly</li>
<li>Perform gene expression assays using RT-PCR</li>
<li>Develop new cell lines by modifying growth factor signaling</li>
<li>Develop assays to screen, isolate, and validate cell lines</li>
<li>Reagent preparation, aliquoting, inventory management</li>
<li>Collaborate with the preclinical team to support preclinical trials of novel technologies</li>
<li>Contribute to various group efforts in research and development</li>
<li>Identify, suggest, purchase and operate supplies and equipment through established processes to support this role</li>
<li>Mentor junior members with technical skills, and experimental design</li>
</ul>
Qualifications &amp; Skills: 
<ul>
<li>Experienced in adherent mammalian cell culture</li>
<li>Experience with molecular cloning and transfection including designing DNA constructs, producing plasmids, and delivering to cells using transfection or electroporation</li>
<li>Cell line development: able to screen, isolate, and validate targeted cell populations</li>
<li>Knowledge of basic cell biology with an ability to develop methods to manipulate</li>
</ul>
We offer great benefits (health, vision, and dental insurance and a retirement plan) and challenging, impactful work. Join our growing team, work with smart and dedicated people, and help develop cutting-edge technologies that will positively impact the world. Job Type: Full-time Salary: From $64,480.00 per year Benefits: 
<ul>
<li>Dental insurance</li>
<li>Health insurance</li>
<li>Paid time off</li>
<li>Retirement plan</li>
<li>Vision insurance</li>
</ul>
Schedule: 
<ul>
<li>8 hour shift</li>
<li>Weekend availability</li>
</ul>
Ability to commute/relocate: 
<ul>
<li>Rancho Cordova, CA 95670: Reliably commute or planning to relocate before starting work (Required)</li>
</ul>
Education: 
<ul>
<li>Bachelor's (Required)</li>
</ul>
Experience: 
<ul>
<li>Mammalian cell culture: 2 years (Required)</li>
</ul>
Work Location: In person

Research Associate Cell Culture & Molecular Biology

<h3>Job Description</h3>
Job Description
TCRCure Biopharma is a clinical-stage biotechnology startup with a global focus to provide personalized cancer immunotherapies. Our product team of scientists and engineers leverage their expertise in CAR-T and TCR-T therapy, high-throughput cloning, and gene therapy to deliver “patient-first immunotherapy.” We are passionate about our technology and we need YOUR help to transform our ideas into cures.
Currently, our research team in Los Angeles is seeking a highly motivated individual to perform hands-on laboratory work. We are looking for someone who can adapt quickly to the rapidly evolving priorities and collaborate effectively with scientists and other associates in the group to help our product development succeed. This position will be based in Los Angeles, CA and the candidate will report to the Senior Scientist.
Responsibilities and Duties
<ul>
<li>T Cell cultures and assays using flow cytometry</li>
<li>Lentivirus and Retrovirus engineering, generation and transduction</li>
<li>CAR-T and In vivo CAR-T cell engineering</li>
<li>Performing PCR, cloning experiments to construct plasmids for T cell therapy</li>
<li>Execution of accurate, up-to-date records of experiments and prompt reporting of results</li>
<li>Maintenance of laboratory equipment</li>
<li>Other duties as assigned</li>
</ul>
Qualifications and Skills
<ul>
<li>B.S. or M.S. with 1-2 years of work experience in cell-based assays; immunology experience is a plus.</li>
<li>Experience in, or familiar with molecular biology techniques, such as PCR, plasmid preparation, cloning, virus production, virus purification, etc.</li>
<li>Working knowledge of molecular biology equipment.</li>
<li>Strong record-keeping skills and attention to detail in following SOPs</li>
<li>Excellent communication and interpersonal skills for working in a small-team collaborative environment.</li>
<li>Comfortable and efficient in a fast-paced, dynamic, and growing environment.</li>
</ul>
<ul>
<li>Desired skills include: (1) Familiarity with flow cytometry, (2) experience handling viral vectors, and (3) familiarity with CAR-T therapy.</li>
</ul>
Benefits
In addition to a competitive base salary, we provide a suite of employee benefits, including health, dental and vision insurance, as well as a matching retirement plan.

Research Associate/Senior Research Associate

<h3>Job Description</h3>
Job Description
We are seeking a highly motivated and qualified individual to join our Exploratory Discovery Department as a Research Associate I and work as part of a team to drive success. Ideal candidates will be self-motivated, independent, committed to the generation of high-quality data within a fast-paced and innovative research team.
The Research Associate I will support the discovery and development of novel delivery strategies to enable extrahepatic siRNA delivery. This position offers an exciting opportunity to contribute to RNA-based drug discovery programs across multiple therapeutic areas. The ideal candidate will help drive innovative approaches that enhance the efficacy, specificity, and safety of siRNA therapeutics for a wide range of complex disease indications. 
Essential Responsibilities:
<ul>
<li>Carry out assigned laboratory functions applying knowledge and skill in an accurate, timely manner.</li>
<li>Conduct in vivo studies in compliance with IACUC protocols and internal SOPs.</li>
<li>Perform routine rodent procedures including dosing via various routes (IV, SC, PO, IP, IVT), physiological monitoring, blood collection (e.g., cheek puncture, tail vein), necropsy and tissue collection</li>
<li>Assist project leads with study scheduling, preparation of study protocols and materials</li>
<li>Manage genetically engineered mouse colonies. Responsibilities include breeding setup and maintenance, plug checking, pregnancy confirmation, weaning, animal identification (e.g., ear punching or tagging), and genotyping via PCR</li>
<li>Conduct pharmacokinetic (PK) and pharmacodynamic (PD) evaluations using ex vivo tissue and blood samples</li>
<li>Accurately document experimental data and maintain well-organized lab notebooks and electronic records.</li>
<li>Maintain and calibrate lab equipment and ensure proper functioning to support study execution</li>
<li>Establish and maintain excellent working relationships with critical collaborative partners throughout the company.</li>
<li>Manage and maintain equipment, reagents and dedicated laboratory environment needed to carry out assignments.</li>
<li>Maintain updated and well-organized lab notebooks.</li>
<li>Execute daily laboratory operations with an approach designed to minimize risks and hazard waste streams.</li>
<li>Maintain all appropriate corporate standards for facility safety and hazardous material management.</li>
<li>Other duties as assigned.</li>
</ul>
Essential Physical Characteristics:
Reasonable accommodation(s) may be made to enable qualified individuals with disabilities to perform the essential functions of a job, on a case-by-case basis.
On-Site Protocol:
Physical presence at the ADARx Pharmaceuticals worksite is a necessary job function of this role, which the Company deems critical to collaboration, innovation, productivity, employee well-being and engagement, and it enhances the Company culture.
Qualifications:
<ul>
<li>BA, BS or Msc degree in Biological Sciences or a related field with a minimum of 2 years of hands-on experience in in vivo pharmacology within an academic, biotech, pharmaceutical, or CRO setting.</li>
<li>Demonstrated proficiency in rodent handling and dosing techniques (IV, SC, PO, IP, IVT).</li>
<li>Experience in blood collection, physiological monitoring, necropsy, and tissue harvesting.</li>
<li>Familiarity with IACUC protocol development and compliance is strongly preferred</li>
<li>Experience with ex vivo assays such as ELISA, western blot, RT-qPCR, and cell culture.</li>
<li>Understanding of project timelines and deliverables and plans/coordinate project work accordingly with departmental, functional, and external stakeholders.</li>
<li>Strong problem-solving skills and a proactive attitude towards exploring new approaches.</li>
<li>Excellent written and verbal communication skills and effective presentation of complex scientific data to cross-functional and senior management teams are essential for this role.</li>
<li>Willingness to work occasional weekends based on study needs.</li>
<li>Proficiency working with Microsoft Office Suite Products.</li>
</ul>
Preferred Qualifications:
<ul>
<li>Prior experience in biotech/pharmaceutical industry a plus.</li>
<li>Prior experience working with genetically engineered mouse models is desirable.</li>
</ul>
Required Key Attributes:
<ul>
<li>Must be able to work independently as well in cross-functional team settings with supervision as needed.</li>
<li>Adaptable / Flexible - willing and able to adjust to multiple demands and shifting priorities as well as an ability to meet day-to-day challenges with confidence and professionalism.</li>
<li>Self-motivated with excellent interpersonal, organizational and communication skills with the ability to take a hands-on approach to work effectively in a dynamic and collaborative, fast-paced environment.</li>
</ul>
Compensation:
<ul>
<li>This is a full-time position, Monday-Friday, occasional overtime.</li>
<li>Pay is commensurate with experience.</li>
<li>Equity-based compensation</li>
<li>Performance-based bonuses</li>
<li>401(k) with Company Match</li>
<li>Medical, Dental, Vision</li>
<li>Flexible Spending Account</li>
<li>Life Insurance</li>
<li>Employee Assistance Program</li>
<li>Employee Discounts </li>
<li>Gym Membership</li>
<li>Paid Vacation</li>
<li>Paid Holidays</li>
<li>Paid Sick, Jury Duty, Bereavement</li>
</ul>
Work Authorization:
<ul>
<li>United States (Required)</li>
<li>Background Check</li>
<li>As a condition of employment, you must successfully complete all post-offer, pre-employment requirements, including but not limited to a background check.</li>
</ul>
Company Overview:
We are a late-stage clinical biotechnology company dedicated to transforming cutting-edge science into next-generation RNA medicines across a wide range of therapeutic areas. Our goal is to control the expression of specific disease drivers with highly selective RNA targeted therapies, delivering life-changing treatments for patients with urgent unmet medical needs.
ADARx Pharmaceuticals is an EEO employer committed to an exciting, diverse, and enriching work environment. We prohibit discrimination and harassment of any kind based on race, color, sex, religion, sexual orientation, national origin, disability, genetic information, pregnancy, or any other protected characteristic as outlined by federal, state, or local laws.

Disclosure Statement:
<ul>
<li>The above statements are intended to describe the general nature and level of work being performed by employees assigned to this classification. They are not intended to be construed as an exhaustive list of all responsibilities, duties and skills required of employees assigned to this position.</li>
<li>Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.</li>
<li>The range provided is based on what we believe is a reasonable estimate for the base salary pay range for this job at the time of posting. This role is eligible for an annual target bonus and annual equity awards. Some roles may also be eligible for overtime pay, in accordance with federal and state requirements. Actual base salary pay will be based on a number of factors, including skills, competencies, type and length of experience within the industry, and other job-related factors permitted by law.</li>
<li>Total Compensation includes base salary; benefits: medical, vision, and dental insurance; life insurance; 401(k) matching program; paid time off; paid holidays; Employee Assistance Program; and other employee benefits. This role may also be eligible for short-term or long-term incentive compensation, including but not limited to cash bonuses.</li>
<li>Following a conditional offer of employment, satisfactory completion of a background check (including criminal records check) is required prior to beginning employment. Any offer of employment may be rescinded if the background check reveals disqualifying information, and/or it is discovered that the candidate knowingly withheld or falsified information. Failure to satisfactorily complete the background check may affect the continued employment of a current NAI employee who was conditionally offered the position.</li>
</ul>

Research Associate I

<h3>Job Description</h3>
Job Description
Job Title:
Science Director – Biophysics
Location: Princeton NJ or Los Angeles CA&nbsp; - must be local to either of these offices or willing to relocate
Vaccination against COVID-19 is a prerequisite for employment at CHDI Management
Salary range: $120,000-220,000.&nbsp; Exact compensation will vary based on experience
Job Description:
CHDI Management seeks an experienced, innovative, and passionate drug discovery scientist to join the preclinical team as Science Director, Biophysics, to support the Foundation’s mission to accelerate meaningful therapies for Huntington’s disease (HD). Partnering with the internal Computational Drug Discovery and Structural Biology Science Director the successful candidate will be a biophysics domain knowledge expert and participate on interdisciplinary teams to advance the understanding of HD biology, to identify and characterize potential HD drug targets and to support the discovery of novel agents for pharmacologic proof-of-concept. The position involves collaborating with internal CHDI scientists, Contract Research Organization (CRO) collaborators, industrial partners and external academic experts.
The position reports to the Vice President, Chemistry
Job Responsibilities:
<ul>
<li>Manage external biophysics resources at CRO partners by providing strategic and technical oversight of biophysical assay deployment across the CHDI project portfolio.</li>
<li>Collaborate with partners including HD biology-focused thematic areas, structural biologists, medicinal chemists and informaticians. Participate as a biophysics domain knowledge expert to interdisciplinary project teams.</li>
<li>Co-develop project workplans as a member of interdisciplinary project teams with strategic line-of-sight to achieve program objectives.</li>
<li>Generate and deliver impactful biophysical data and insight to characterize biomolecular interactions and provide discovery teams with detailed interaction analyses (e.,&nbsp;protein-compound, nucleic acid-compound, protein-protein, and protein-nucleic acid) in cell-free and cellular systems.</li>
<li>Develop and deploy ligand-protein interaction experiments using biophysical methods (e.g. SPR, ITC, NMR, thermal shift, native MS) to measure binding of small molecule hits and leads to potential drug targets.</li>
<li>Design and conduct experiments to deconvolute biophysical mechanisms of active agents to understand residence time, predict efficacy and pharmacology, and select the best molecules for pharmacologic proof-of-concept.</li>
<li>Collaborate with the Research Informatics and Computational Drug Discovery team to prepare, organize, combine and integrate biophysics data and accelerate the development of tool compounds</li>
<li>Identify and partner with external collaborators (CRO, academic) to develop impactful, cutting-edge biophysical methods for their strategic application to projects in support of Foundation objectives.</li>
</ul>
Qualifications:
<ul>
<li>PhD. in Biophysics, Biophysical Chemistry, Chemistry and Chemical Biology or a related discipline.</li>
<li>6 plus years of industry experience in target validation and/or integrated drug discovery projects.</li>
<li>Demonstrated expertise in the use of biophysical methods (SPR, GCII, HTRF, MST, AS-MS, SwitchSense and thermal stability assays such as DSF) for characterization of biomolecular interactions (protein-compound, nucleic acid-compound, protein-protein, and/or protein-nucleic acid).</li>
<li>Experience in designing and building mechanistic assays to support elucidation of novel disease-relevant biology and target validation.</li>
<li>Experience in the application of emerging biophysical methods (e.g., single-molecule fluorescence microscopy, single-molecule force microscopy, magnetic force microscopy to interrogate macromolecular assemblies within their native environment highly preferred.</li>
<li>Experience working in a multidisciplinary team-oriented environment.</li>
<li>Excellent written and oral communication skills.</li>
<li>Experience in oversight of CRO collaborators.</li>
</ul>
About CHDI Foundation, Inc.
CHDI Foundation, Inc. is a privately-funded, not-for-profit, biomedical research organization that is exclusively dedicated to rapidly discovering, accelerating and developing therapies that slow the progression of Huntington’s disease (HD). Our scientists work closely with a network of more than 600 researchers in academic and industrial laboratories around the world in the pursuit of these innovative therapies, providing strategic scientific direction to ensure that our common goals remain in focus. This helps bridge the translational gap that often exists between academic and industrial research pursuits and that adds costly delays to therapy development. In its role as a collaborative enabler, CHDI seeks to bring the right partners together to identify and address critical scientific issues and move drug candidates to clinical evaluation as rapidly as possible. Our activities extend from exploratory biology to the identification and validation of therapeutic targets, and from drug discovery and development to clinical studies and trials. More information about CHDI can be found at&nbsp;<a href="http://www.chdifoundation.org" target="_blank">www.chdifoundation.org</a>
About CHDI Management, Inc.
CHDI Management, Inc. was established in 2002 to provide administrative, management and grant making services to CHDI Foundation, Inc.
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Director, Biophysics (Los Angeles CA or Princeton NJ)

<h3>Job Description</h3>
Job Description
Mission Statement
The Salvation Army, an international movement, is an evangelical part of the universal Christian church. Its message is based on the Bible. Its ministry is motivated by the love of God. Its mission is to preach the gospel of Jesus Christ and to meet human needs in His name without discrimination.
Position Summary
The Director of Design Strategy &amp; Research is a foundational leadership position within The Salvation Army’s Center of Applied Research and Innovation (CARI) and champions a cutting-edge “human-centered design” focus within the organization. This pivotal role strategically bridges human-centered design, participatory research, innovation practices, continuous improvement, and faith-rooted service in alignment with The Salvation Army’s mission and the operational framework at the Center of Hope in Anaheim, California. This position will also strengthen CARI’s ability to secure grants and new funding opportunities.
As CARI's program design leader, this role is critical to ensure The Salvation Army’s programs are informed by lived experience, shaped by ethical research practices, and driven by rigorous, actionable insights that improve outcomes for vulnerable communities. The Director will help translate real-time learning from the Center of Hope in Anaheim into scalable innovations that can be shared across the Salvation Army – Orange County, and possibly other Salvation Army locations in the Western Territory.
Essential Functions
<ul>
<li>Leads the creation of CARI’s research and innovation plans, focusing on researching, designing and testing new services that prioritize people’s needs and align with The Center of Hope’s Homeless Throughput</li>
<li>Collaborates with leadership, staff, and community members to set a CARI research agenda that encourages new ideas for addressing homelessness and other critical social</li>
<li>Identifies and defines new interdisciplinary research projects that consider real-life experiences, equity, and faith-based</li>
<li>Contributes to CARI fundraising efforts by helping secure new grants and also demonstrating impact through compelling program design, outcome-based evidence and impactful storytelling</li>
<li>Builds partnerships with research groups and innovation experts to adopt leading design</li>
<li>Establishes and oversees CARI’s approach to program design, leading research to improve services at the Center of Hope in Anaheim and also sharing successful practices with other Salvation Army locations as</li>
<li>Facilitates participatory workshops to ensure service users can contribute to and shape</li>
<li>Develops and manages internal CARI research systems, including ethics protocols, participant engagement frameworks, and impact measurement</li>
<li>Translates research findings into practical guides and tools for decision-making by Salvation Army leaders and</li>
<li>Ensures ethical handling of community knowledge and data in line with Salvation Army</li>
<li>Mentors and supervises staff, fellows, and interns in human-centered design, community-based research, and ethical</li>
<li>Other assignments and tasks as</li>
</ul>
Working Conditions
Ability to walk, stand, bend, squat, climb, kneel, and twist on an intermittent or sometimes continuous basis. Ability to grasp, push, pull objects such as files, file cabinet drawers, and reach overhead. Ability to operate computer, fax, and telephone. Ability to lift up to 40 lbs.
Minimum Qualifications
<ul>
<li>By virtue of its direct contact with, and representation to people who engage in Salvation Army programs, people who demonstrate an understanding of The Salvation Army’s Christian mission are required for this position.</li>
<li>Doctoral Degree in Human-Centered Design, Social Work, Public Health, Policy, or a related field. Preferred: Doctor of Social Work with a focus on innovation and systemic change.</li>
<li>Minimum 10+ years of progressive experience leading human-centered design research and implementation and cross-sector strategy efforts in nonprofit, government or academic settings.</li>
<li>Demonstrated ability to lead ethical human- centered design research, especially among vulnerable and underserved populations.</li>
<li>Skilled in translating design research insights into programmatic strategies that inform policy, strengthen systems, and drive measurable social outcomes.</li>
<li>Experienced in strategic planning, developing multi-year innovation roadmaps, and aligning research and design priorities with organizational mission and long-term goals.</li>
<li>Deep understanding of trauma-informed care, community engagement, and system-level change.</li>
<li>Proven success in designing scalable models and frameworks that can be replicated across sites, including development of playbooks, toolkits, and Communities of Practice to support broad implementation.</li>
<li>Adept at fostering collaboration across diverse teams, building internal capacity, and mentoring emerging leaders in research, innovation, and social impact.</li>
</ul>
Skills, Knowledge and Abilities
<ul>
<li>Demonstrated leadership in human-centered design, applied social research, or innovation within complex social systems. Preference will be given for candidates who have taught human- centered design courses at a University-level.</li>
<li>Mastery of mixed methods research, user research, service design, applied research and ethical engagement with vulnerable or underserved populations.</li>
<li>Exceptional facilitation, partnership, and communication skills across diverse teams and stakeholders.</li>
<li>Understands how research involving people is reviewed and approved to protect participants (IRB processes).</li>
<li>Is familiar with ways to turn research findings into real-world actions or changes (evidence-to- action frameworks).</li>
<li>Ability to balance strategic vision with hands-on implementation in dynamic, mission-driven settings.</li>
<li>Driving Test and clean MVR check.</li>
<li>If working in the vicinity of children a criminal background check is required with certification for Protect the Mission policies and procedures.</li>
<li>Must have the ability to work with, direct, and relate well with co-workers, community partners/members, and guests/clients.</li>
<li>Able to function and thrive in a fast-paced, frequently evolving environment.</li>
<li>Excellent computer skills: must be able to utilize all necessary office equipment adequately (i.e. computers, copy machines, scanners, calculator, etc.).</li>
<li>Excellent organizational skills; highly self- motivated and detail oriented.</li>
<li>Must have outstanding written and verbal communication skills.</li>
<li>Professional and courteous; excellent presentation skills</li>
</ul>

Director of Design Strategy & Research-11-145-SC/Orange County

<h3>Job Description</h3>
Job DescriptionCompany Description 
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at&nbsp;<a href="http://www.abbvie.com" target="_blank">www.abbvie.com</a>. Follow @abbvie on&nbsp;X,&nbsp;Facebook,&nbsp;Instagram,&nbsp;YouTube,&nbsp;LinkedIn&nbsp;and&nbsp;Tik Tok.
Job Description 
**This is a hybrid position (3days a week on-site/2days remote). Candidates must be local and work hybrid out of San Francisco, CA; Irvine, CA; Lake County, IL; Florham Park, NJ&nbsp;
The Statistical Analyst is an integral role in the research and development of new pharmaceutical products. The primary responsibilities for this role include the analysis and reporting of clinical trial data without supervision for routine activities and with supervision for more complex activities. The Statistical Analyst interfaces with Statistics, Clinical Data Strategy &amp; Operations and Development Operations.
Responsibilities
<ul>
<li>Leads the statistical programming activities for routine studies.</li>
<li>Create documentation for regulatory filings including reviewers guides and data definition documents</li>
<li>Participate in the development of standard SAS Macros, as well as, presenting information on existing Macros</li>
<li>Pharmacometrics Only: Consolidate heterogeneous data sources (e.g. clinical study databases, external databases, real world data) to prepare analysis-ready data sets within a defined quality control process supporting a particular study.</li>
<li>Perform exploratory data analyses and visualizations in interaction with the clinical pharmacologist or pharmacometrician.</li>
<li>Produce dynamic and static data visualizations to communicate quantitative analyses.</li>
<li>Statistics Only: Develop SAS programs for the creation of ADaM data sets following CDISC standards.</li>
<li>Develop SAS programs for the creation of Tables, Listings and Figures.</li>
<li>Validation of ADaM data sets. Validation of Tables, Listings and Figures.</li>
<li>Create specifications for the structure of ADaM data sets for individual studies and integrated data</li>
</ul>
Qualifications 
<ul>
<li>MS in Statistics, Computer Science or a related field with 2+ years of relevant experience. OR BS in Statistics, Computer Science or a related field with 4+ years of relevant experience.</li>
<li>Demonstrated practical understanding of SAS programming or NONMEM concepts and techniques related to drug development.</li>
<li>Basic understanding of CDISC Standards.</li>
<li>Basic understanding of the drug development process.</li>
<li>Ability to communicate clearly both oral and written.</li>
</ul>
 Additional Information 
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or&nbsp;local law:&nbsp;​
<ul>
<li>
The compensation range described below is the range of possible base pay compensation that the Company&nbsp;believes in&nbsp;good faith it will pay for this role at the time&nbsp;ofthis posting based on the job grade for this position.&nbsp;Individual&nbsp;compensation paid within this range will depend on many factors including geographic location,and&nbsp;we&nbsp;may ultimately&nbsp;pay more or less than the posted range. This range may be modified in the&nbsp;future.&nbsp;​
</li>
<li>
We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),&nbsp;medical/dental/vision&nbsp;insurance and 401(k) to eligible&nbsp;employees.​
</li>
<li>
This job is eligible to participate in our short-term incentive&nbsp;programs.&nbsp;​
</li>
<li>
This job is eligible to participate in our long-term incentive&nbsp;programs​
</li>
</ul>
Note: No amount of pay&nbsp;is considered to be&nbsp;wages or compensation until such amount is earned, vested, and&nbsp;determinable.&nbsp;The amount and availability of anybonus,&nbsp;commission, incentive, benefits, or any other form of&nbsp;compensation and benefits&nbsp;that are allocable to a particular employee remains in the Company's soleand&nbsp;absolute&nbsp;discretion unless and until paid and&nbsp;may be modified at the Company’s sole and absolute discretion, consistent with&nbsp;applicable law.&nbsp;
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community.  Equal Opportunity Employer/Veterans/Disabled.&nbsp;
US &amp; Puerto Rico only - to learn more, visit&nbsp;<a href="https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html" target="_blank">https://www.abbvie.com/join-us/equal-employment-opportunity-employer.ht…</a>
US &amp; Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
<a href="https://www.abbvie.com/join-us/reasonable-accommodations.html" target="_blank">https://www.abbvie.com/join-us/reasonable-accommodations.html</a>

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