field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Position Summary Antibody AIDD (Principal Scientist), is responsible for leading a computational science team focused on biologics discovery. This role will provide critical support for the discovery and engineering of antibodies, fusion proteins, and other large-molecule therapeutics by applying and developing cutting-edge computational biology, structural biology, and AI technologies. The leader must be a technical expert capable of leading a team and collaborating closely with experimental teams in antibody engineering and protein sciences to solve core challenges in affinity, specificity, stability, and developability.
Key Responsibilities
<ul>
<li>Team Leadership &amp; Management: Lead and develop a team of 2-4 computational biologists, fostering a scientifically rigorous and collaborative work environment.</li>
<li>Project Scientific Leadership: Serve as the core computational lead for biologics projects, directing the formulation and execution of computational strategies, including computational antigen design, antibody/protein design and optimization, and epitope prediction.</li>
<li>Developability Assessment: Lead the team in establishing and applying high-throughput computational predictive models to systematically assess and optimize the developability of candidates (e.g., immunogenicity, aggregation, viscosity) at early discovery stages to de-risk downstream development.</li>
<li>Technology Innovation &amp; Platform Development: Track the latest advances in AI for biologics design; lead the development and validation of new algorithms and workflows for protein design, structure prediction, and property prediction, and promote their deployment on internal platforms.</li>
<li>Cross-Functional Collaboration: Collaborate closely with teams in Antibody Discovery, Protein Sciences, Bioanalytics, and Formulation Development to form an efficient "design-build-test-learn" R&amp;D cycle.</li>
</ul>
 
Basic Qualifications
<ul>
<li>Ph.D. in Computational Biology, machine learning, Structural Biology, Biophysics, or a related field.</li>
<li>5+ years of experience in biologics R&amp;D within the pharmaceutical or biotechnology industry.</li>
<li>Excellent programming skills in Python or R and experience with relevant bioinformatics and structural biology software.</li>
<li>A solid theoretical and practical foundation in protein structure modeling and molecular dynamics simulations.</li>
</ul>
Preferred Qualifications
<ul>
<li>Structural Modeling &amp; De Novo Design:</li>
<li>Deep expertise in protein structure prediction (e.g., AlphaFold2/Multimer), protein-protein docking, and loop modeling.</li>
<li>Extensive experience using computational protein design platforms like Rosetta for de novo design, stability engineering, and binder design.</li>
<li>Biophysics Simulation: Advanced knowledge and practical experience in running and analyzing all-atom molecular dynamics (MD) simulations of complex biologics (e.g., antibodies, bispecifics) to assess dynamics, stability, and aggregation propensity.</li>
<li>AI for Biologics:</li>
<li>Familiarity and hands-on experience with modern AI methods, such as Protein Language Models (e.g., ESMFold, ProGen).</li>
<li>Experience applying diffusion- or generative models for protein sequence and structure design.</li>
<li>Knowledge of Graph Neural Networks (GNNs) for protein function prediction or developability assessment.</li>
<li>Bioinformatics &amp; Multi-Omics Integration: Proficiency in advanced sequence analysis, structural bioinformatics, and experience integrating multi-omics data (e.g., genomics, proteomics) for target identification and validation.</li>
<li>Breadth &amp; Depth of Project Experience:</li>
<li>A proven track record of leading computational efforts for antibody de novo design and affinity maturation.</li>
<li>Verifiable contributions to solving specific developability issues for multiple biologic formats (e.g., mAbs, VHHs, bispecifics, ADCs).</li>
</ul>

Principal Scientist of AI-Driven Protein design

<h3>Job Description</h3>
About Us: 
 
Avails Medical, Inc. is a medical device start-up, based in Menlo Park, California. At Avails we are developing a novel electrical point-of-care bio-sensor platform for rapid infectious disease detection and antibiotic susceptibility testing.
Description: This is a full-time position
 
As part of our ongoing growth, we have an opening for a full-time Microbiology Lab Technician. Under supervisor or senior technical support direction the Lab Tech for Microbiology will assist and process specimens and load them onto testing instruments; assist in instrument maintenance; assist in general laboratory prep and maintenance; archive samples after analysis; monitor equipment temperature readings; participate in test development and ad-hoc projects as directed.
 
Responsibilities:
<ul>
<li>Culturing and maintenance of bacterial cell cultures, ensuring proper growth conditions and viability</li>
<li>Prepare lab supplies and equipment for experiments.</li>
<li>Preparing and aliquoting of antibiotic stocks, reagents, media, and buffers aseptically</li>
<li>Decontamination and cleaning of labware, general lab cleaning and maintenance, and lab equipment maintenance</li>
<li>Restocks and/or distributes supplies to the appropriate areas of the lab</li>
<li>Maintain logs and QC records for laboratory equipment in accordance with company and regulatory requirements.</li>
<li>May assist in processing specimens for testing and recording test results in an organized fashion.</li>
<li>May assist and perform a variety of bacterial experiments and testing in collaboration with other technicians, research associates, scientists, and engineers.</li>
<li>Effectively communicates project status to supervisor, peers and other staff.</li>
<li>Performs other duties as needed.</li>
<li>In addition to an employee’s typical work schedule, this position may require employees to work weekends, split shifts, varying shift schedules, and holidays if needed by the Company.</li>
</ul>
Education &amp; Experience Requirements:
<ul>
<li>Bachelor's degree in Microbiology or related field with basic microbiology lab experience.</li>
<li>Basic experience in Microbiology, in particular, aseptic technique and microbiological sub-culturing.</li>
<li>Preference for experience in an industrial microbiology or related laboratory environment, such as working in Biosafety Level-2 (BSL-2) rated spaces.</li>
</ul>
 
Required Skills:
<ul>
<li>Microbiology</li>
<li>Proficient in Microsoft Excel</li>
<li>Excellent aseptic technique</li>
</ul>
 
Personal Traits:
<ul>
<li>Problem solving and trouble-shooting skills to work with colleagues to identify and execute appropriate experimental design to generate accurate data.</li>
<li>Strong team player, with a collaborative and helpful mindset.</li>
<li>Ability to work independently with supervision to execute detailed tasks, operations, procedures, and experiments while maintaining a safe, effective microbiology laboratory.</li>
<li>Some flexibility required for evening and/or weekend shift</li>
</ul>

Microbiology Laboratory Technician

<h3>Job Description</h3>
Description
Are you a motivated Principal Resilient Systems Scientist with a technical vision and hands-on knowledge of mission-focused systems? The Leidos Innovations Center’s newly established Information and Data Science Division is seeking a Senior Resilient Systems Scientist to help lead strategic solution developments and projects. This role will drive capture of strategic customer-funded software R&amp;D. The ideal candidate will have a proven track record in developing technology-based approaches that yield novel, innovative capabilities while advancing the state of the art. We are looking for a proven researcher who can develop and lead a groundbreaking research portfolio using both internal and customer funding.&nbsp;
Please note: This is an on-site role. The ideal candidate will be able to work out of our San Diego, CA; Arlington, VA or Dayton, OH offices.&nbsp;Occasional opportunity to telework may be available.
Primary Responsibilities&nbsp;
<ul>
<li>Develop innovative solutions to challenging problems of interest to the Defense Applied Research Projects Agency (DARPA) and U.S. Department of Defense (DoD). &nbsp;</li>
<li>Engaging R&amp;D customers and transition partners to understand technical gaps and needs for resilient systems solutions in mission critical systems.&nbsp;</li>
<li>Lead and execute research in areas of naval surface platforms, autonomy, and resilient systems.</li>
<li>Develop and deliver software products.</li>
<li>Leading teams of researchers and engineers in the development, adaptation, and extension of innovative approaches to resilient systems solutions across a range of technical areas and application domains to advance the state of the art while addressing long-term problems of importance to national security such as embedded systems.&nbsp;</li>
<li>Develop novel approaches for the generation of assurance evidence for critical software, at scale&nbsp;</li>
<li>Collaborate in cross-discipline teams to deliver innovations that provide measurable resilient mission impact.&nbsp;</li>
<li>To ensure technical relevancy, they will track software technology trends in the customer community and broader R&amp;D communities as well as identify future software R&amp;D funding opportunities.&nbsp;</li>
</ul>
Basic Qualifications&nbsp;
<ul>
<li>Bachelor’s degree in Computer Science, Mathematics, or a related field and 12+ years prior relevant experience, M.S degree with 10+ years of prior relevant experience, or Ph.D. with 8+ years of experience (Ph.D. preferred).</li>
<li>Must be a US Citizen.</li>
<li>Qualified candidates MUST possess a Secret clearance as well as have the ability to obtain a TS/SCI.</li>
<li>Proven track record in proposing, winning, and executing work with customers such as DARPA, IARPA or similar agencies within the last 5 years.</li>
<li>Proven track record in developing and delivering software products.</li>
<li>Experience with surface platforms, autonomous concepts, and naval applications.</li>
<li>Industrial and/or academic experience advancing the state of the art in FPGA development, embedded systems, formal verification, developing technologies such as program analysis, constraint-solving, symbolic execution, or theorem proving.</li>
<li>Experience with autonomous systems.</li>
<li>Experience with naval systems and specifically surface vessels.</li>
<li>Proven track record in proposing, winning, and executing Contract R&amp;D.</li>
<li>At least 4 years of experience with programming languages such as Java, Scala, C/C++, Ruby, Rust, or Python.</li>
<li>Experience with test and evaluation, software analysis and software specification.</li>
<li>Strong verbal and written communication skills, with experience engaging with senior leadership and technical teams as well as ability to present complex software solutions in a clear, understandable manner.</li>
</ul>
Preferred Qualifications&nbsp;
<ul>
<li>Ph.D. in Computer Science, Mathematics, or related degree&nbsp;</li>
<li>FPGA development and testing, embedded systems design and innovation, applying formal methods, using technologies such as theorem provers for first-order logic and higher-order logic, proof assistants, solvers, or other automated reasoning tools&nbsp;&nbsp;</li>
<li>Experience conducting applied research areas of CPS such as autonomous vehicles, smart sensors, or Internet of Things, fusing data collected from cyber and physical systems to develop novel approaches to address emerging technical challenges in domains relevant to U.S. national security&nbsp;</li>
<li>Experience in semantic analysis of software&nbsp;</li>
<li>Strong and proven customer relationship skills including the ability to discover the true technical challenges and requirements associated with opportunities, recommending alternative technical approaches, and shaping future opportunities&nbsp;</li>
<li>Experience applying and leading the application of formal methods in fundamental research contexts, to problems in complex domains, under conditions of uncertainty, and dynamic and evolving technical challenges&nbsp;</li>
<li>Ability to work in a fast-paced environment&nbsp;</li>
<li>Excellent written and oral skills in communicating technical information with an ability to present complex technical information clearly and coherently&nbsp;</li>
<li>Proven experience forming strong teams composed of members from academia and industry for competitive research and development opportunities&nbsp;</li>
<li>Experience developing software for critical applications that require software certification&nbsp;</li>
</ul>
LInC
Original Posting:July 18, 2025
For U.S. Positions: While subject to change based on business needs, Leidos reasonably anticipates that this job requisition will remain open for at least 3 days with an anticipated close date of no earlier than 3 days after the original posting date as listed above.
Pay Range:Pay Range $126,100.00 - $227,950.00
The Leidos pay range for this job level is a general guideline only&nbsp;and not a guarantee of compensation or salary. Additional factors considered in extending an offer include (but are not limited to) responsibilities of the job, education, experience, knowledge, skills, and abilities, as well as internal equity, alignment with market data, applicable bargaining agreement (if any), or other law.

Principal Autonomy and Resilient Systems Scientist

<h3>Job Description</h3>
Location: Irvine, CA
 
Join our client, a groundbreaking startup. We're seeking a dynamic R&amp;D Scientist/Organic Chemist to be part of our pioneering team, focusing on atmospheric water harvesting and CO2 capture technologies. This role offers the exciting opportunity to work on the synthesis and analysis of MOF, COF, and other supramolecular materials, directly impacting environmental sustainability.
 
Why You Should Apply
<ul>
<li>Contribute to the cutting-edge field of MOF/COF-based technologies.</li>
<li>Collaborate with top-tier research teams, including partnerships with University of California, Berkeley.</li>
<li>Engage in diverse roles from synthesis to analysis of advanced materials.</li>
<li>Opportunity to mentor and lead in a fast-paced, innovative startup environment.</li>
</ul>
 
What You’ll Be Doing
<ul>
<li>Synthesizing various MOF &amp; COF materials and characterizing their properties.</li>
<li>Collaborating closely with the R&amp;D head to develop commercial-grade technologies.</li>
<li>Utilizing advanced analytical techniques for material characterization.</li>
<li>Developing synthetic processes for organic ligands at a commercial scale.</li>
<li>Engaging in collaborative research and intellectual property creation.</li>
</ul>
 
About You
<ul>
<li>PhD in organic chemistry with a strong research background.</li>
<li>Industry experience in organic synthetic chemistry need, MOF/COF experience NOT neccessary</li>
<li>Demonstrated track record in research and scale-up prototypes.</li>
<li>Strong commitment to safety, operational excellence, and teamwork.</li>
</ul>
 
How To Apply
We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to <a href="mailto:js@scientificsearch.com" target="_blank">js@scientificsearch.com</a> and tell us why you’re interested. Or, feel free to email your resume. Please include Job#19434.

R&D Chemist

<h3>Job Description</h3>
Job DescriptionCompany Description 
Consider joining Lancaster Laboratories where people are the most important element in our chemistry.&nbsp; Celebrating 50 years of service, Lancaster Laboratories is a leading contract lab providing testing and research services in the environmental, pharmaceutical, and biopharmaceutical sciences to clients worldwide.
Job Description 
The Ideal Candidate would possess:​
<ul>
<li>2+ years of quantitative analytical HPLC experience</li>
<li>Experience conducting routine laboratory experiments e.g. HPLC, DSC, PXRD spectroscopy, solubility determinations, dissolution testing, suspension processing, etc. in a timely and productive manner with consistent quality output.</li>
<li>Ability to follow procedures reliably and consistently and ability to&nbsp; recognize and elevate relevant issues as appropriate</li>
<li>Strong computer, scientific, and organizational skills</li>
<li>Excellent communication (oral and written) and attention to detail, ability to work independently and as part of a team, self-motivation, adaptability, and&nbsp;a&nbsp;positive attitude</li>
</ul>
Qualifications 
Qualifications
<ul>
<li>Associate’s or Bachelor’s degree in Chemistry or other related degree concentration</li>
<li>2+ years of related experience</li>
<li>Authorization to work in the United States indefinitely without restriction or sponsorship</li>
<li>Candidates in commutable distance to La Jolla, CA are recommended to apply.</li>
</ul>
 Additional Information 
What we offer:
<ul>
<li>Excellent full time benefits including comprehensive medical coverage, dental, and vision options</li>
<li>Life and disability insurance</li>
<li>401(k) with company match</li>
<li>Paid vacation and holidays</li>
<li>Career Development and continuing education opportunities</li>
<li>Compensation Range: $52,000 - $55,000</li>
</ul>
Position is full-time, 8am - 5pm with occasional overtime required.&nbsp;&nbsp;
&nbsp;Eurofins Lancaster Laboratories Professional Scientific Services®&nbsp;(PSS) is a global, award-winning insourcing solution that places our people at our clients’ site dedicated to running and managing laboratory services while eliminating headcount, co-employment and project-management worries.
We infuse our 55-year track record of scientific and laboratory operations expertise, as well as HR and great place to work best practices, to recruit, hire, train and manage highly qualified scientists to perform laboratory services using our client’s quality systems and equipment.
Eurofins USA PSS Insourcing Solutions is a Disabled and Veteran Equal Employment Opportunity employer.

Associate Formulations Scientist

<h3>Job Description</h3>
Job DescriptionJob Title: Lab Manufacturing AssociateJob Description
The 3rd shift Lab Manufacturing Associate will perform a variety of tasks related to the production of reagents and buffers. This includes troubleshooting formulations, filling processes, packaging, and conducting quality control procedures for consumables. The role involves data collection and analysis, processing work orders, executing batch records, and improving SOPs. The associate is expected to identify weaknesses in formulations and SOPs, maintain inventory through cycle counts, and operate in a fast-paced environment with rapidly shifting priorities. Collaboration with a multi-disciplinary team to support R&amp;D and process improvement activities is essential.
Responsibilities
<ul>
<li>Perform assigned manufacturing tasks for reagents and buffers.</li>
<li>Troubleshoot formulations, filling processes, packaging, and analytical techniques.</li>
<li>Conduct quality control procedures for consumables.</li>
<li>Collect and analyze data.</li>
<li>Process work orders to complete products for inventory.</li>
<li>Execute and improve batch records and SOPs.</li>
<li>Identify gaps and weaknesses in SOPs and formulations.</li>
<li>Maintain correct inventory of materials through cycle counts, ordering, and receipt.</li>
<li>Operate in a fast-paced environment with rapidly shifting priorities.</li>
<li>Collaborate with scientists, engineers, and manufacturing personnel to support R&amp;D and process improvement activities.</li>
<li>Lead support for kit operations and buffer formulation under 50L.</li>
<li>Perform troubleshooting as needed.</li>
</ul>
Essential Skills
<ul>
<li>Experience with formulations, reagents, and quality control.</li>
<li>General laboratory skills including UV VIS.</li>
<li>Experience with SOPs, BRs, and WIs.</li>
<li>Hands-on experience with pH, conductivity meter, UV-vis, and other standard lab equipment.</li>
<li>Strong analytical, verbal, and written communication skills.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Self-motivated with the ability to work independently and in teams.</li>
<li>Highly organized and flexible.</li>
<li>Detail-oriented.</li>
<li>Experience with developing and updating BOMs is preferred.</li>
<li>Experience with formulation, fill, packaging, and chromatography in a laboratory setting is preferred.</li>
<li>Bachelor of Science degree in biology, biochemistry, chemistry, molecular biology, or related life science discipline preferred.</li>
<li>1-2 years of relevant experience in consumable manufacturing.</li>
</ul>
Pay and Benefits
The pay range for this position is $23.00 - $23.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in San Diego,CA.
Application Deadline
This position is anticipated to close on Aug 15, 2025.
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email <a href="mailto:actalentaccommodation@actalentservices.com" target="_blank">actalentaccommodation@actalentservices.com</a> for other accommodation options.

Lab Manufacturing Associate

<h3>Job Description</h3>
Job DescriptionJob Title: CMM Programmer and Metrology TechnicianJob Description
As a Metrology Technician, you will play a vital role in providing quality inspection skills to support the company in achieving optimal levels of safety, quality, productivity, and delivery, ensuring both internal and external customer success. You will be responsible for developing, qualifying, and maintaining CMM programs and operating CMMs for First Piece Inspection and Production Approval. Your expertise in reading drawings to determine specifications and tolerances for a variety of components will be essential in ensuring containment activities take place when discrepancies are identified.
Responsibilities
<ul>
<li>Develop and maintain CMM programs using Polyworks or Calypso, transitioning parts from blueprint stage to scanned models.</li>
<li>Operate CMMs for First Piece Inspection and Production Approval.</li>
<li>Read drawings to determine specifications and tolerances for components.</li>
<li>Ensure containment activities occur when discrepancies are identified.</li>
<li>Review and refine data collection requirements according to customer drawings and PPAP requirements.</li>
<li>Participate in corrective action and preventive action processes.</li>
<li>Conduct Gage R &amp; R studies.</li>
<li>Utilize various inspection tools to complete dimensional reports.</li>
<li>Occasionally lift up to 50 pounds.</li>
</ul>
Essential Skills
<ul>
<li>CMM programming experience, preferably 5 years.</li>
<li>Proficiency in FARO Arm, Polyworks, Calypso, GD&amp;T.</li>
<li>Strong computer skills.</li>
<li>Ability to read and interpret blueprints and schematics.</li>
<li>Experience in calibration and inspection.</li>
</ul>
Additional Skills &amp; Qualifications
<ul>
<li>Experience in automotive, medical device, or aerospace industries.</li>
<li>Background in GD&amp;T-based companies and familiarity with Polyworks software.</li>
<li>Experience exceeding goals and aligning with company values.</li>
<li>Proficiency in programming and inspection.</li>
</ul>
Why Work Here?
Join a team that prides itself on delivering vital medical supplies quickly to remote areas with limited access. Benefit from our Apprenticeship Program, Diversity Program, and Professional Development opportunities. Enjoy perks like free lunch &amp; snacks, company social events, and a pet-friendly workplace.
Work Environment
You will work an AM shift with hours typically from 7am to 4pm, although start times may vary slightly based on production needs. This is a fast-paced environment where collaboration and flexibility are essential to meet the demands of pushing parts out efficiently.
Job Type &amp; Location
This is a Contract to Hire position based out of South San Francisco, California.
Pay and Benefits
The pay range for this position is $50.00 - $70.00/hr.
Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:
 • Medical, dental &amp; vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life &amp; AD&amp;D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)
Workplace Type
This is a fully onsite position in South San Francisco,CA.
Application Deadline
This position is anticipated to close on Aug 15, 2025.
About Aerotek:
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meets their goals, skills and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role solving for companies’ construction, manufacturing and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are everything spirit to the test as your career continues to grow.
Aerotek offers weekly pay, employee benefits including medical, dental &amp; vision, life insurance, health advocacy and employee assistance programs, a 401(k) plan, and employee discounts.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Company DescriptionWe know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow. 
<h3>Company Description</h3>
We know that finding work is hard, and finding meaningful work is harder. Aerotek connects 180,000+ light industrial and skilled trades workers with 14,000+ employers each year, helping our workers navigate an evolving labor market and find jobs that meet their goals, skills, and interests. Since 1983, we have provided a variety of career opportunities across North American industry – from short-term assignments at Fortune 500 companies where you can build your skills, to long-term opportunities where you can play a vital role in solving companies’ construction, manufacturing, and maintenance challenges. Our 1,500+ experienced recruiters across 250+ offices work relentlessly to put our workforce in a position to thrive. Let us rise to meet your challenges and put our people-are-everything spirit to the test as your career continues to grow.

Metrology Technician

<h3>Job Description</h3>
Job Description
Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe, and the United States. Today, we're advancing programs in Endocrinology Rare Disease and Oncology.
Here at Ascendis, we pride ourselves on exceptional science, visionary leadership, and skilled and passionate colleagues.
Guided by our core values of Patients, Science, and Passion, we use our TransCon® drug development platform to fulfill our mission of developing new and potentially best-in-class therapies to address unmet medical needs.
Our culture fosters a place where skilled, adaptable, and highly resourceful professionals can truly make their mark. We offer a dynamic workplace for employees to grow and develop their skills.
The Senior Clinical Scientist is involved in the design, monitoring, and data analysis of the Company’s late-phase clinical trials studying growth hormone, parathyroid hormone, and/or C-type natriuretic peptide therapies. As such, the Senior Clinical Scientist is an important and visible member of the Clinical Development team. The Senior Clinical Scientist position is based in the United States ideally the Scientist will work hybrid from our Palo Alto, CA office but we may consider a remote arrangement for the right candidate.
Key Responsibilities
<ul>
<li>For clinical trials: design, provide oversight, and support site and subject retention </li>
<li>Ensure successful completion of documents (including clinical trial protocols, investigator brochures, monitoring plans, site training materials, clinical study reports, health authority responses, standard operating procedures, etc.) with cross-functional team members</li>
<li>Participate on study teams and cross-functional teams as appropriate, and as delegated by the Vice President, Clinical Development</li>
<li>Ensure consistent use of language and criteria across multiple endocrine projects </li>
<li>Ensure study integrity, and track accumulating safety and efficacy data</li>
<li>Anticipate obstacles within a clinical trial, and implement solutions</li>
<li>Analyze, evaluate, and support accurate interpretation and reporting of clinical data</li>
<li>Contribute to drafting and reviewing clinical documents, manuscripts, presentations, and regulatory submissions </li>
<li>Maintain up-to-date knowledge of relevant science, medical information, good clinical practices, and regulatory guidance</li>
<li>Collaborate with—and serve as a clinical research resource for—cross-functional colleagues to optimize product development</li>
<li>Cultivate relationships with investigative sites, clinical consultants, and key opinion leaders to represent the interests of the company</li>
<li>Support corporate strategic and organizational initiatives</li>
<li>Assist with commercial activities as needed</li>
<li>Complete assigned tasks thoroughly, accurately, and on time</li>
<li>Adhere to rigorous ethical standards </li>
<li>Travel up to 20% domestically and internationally for scientific meetings</li>
</ul>
Requirements
<ul>
<li>Advanced degree e.g. Ph.D., Pharm.D., MS, or equivalent</li>
</ul>
<ul>
<li>Strong track record of scientific and clinical inquiry</li>
<li>Understand statistical concepts and clinical trial design</li>
<li>Understand the connection between nonclinical data and clinical data</li>
<li>Possess excellent communication skills (both written and verbal)</li>
<li>Learn quickly, follow complex directions under pressure </li>
<li>Multi-task while remaining organized and attentive to detail</li>
<li>Work hard, be a trustworthy and collaborative team player</li>
<li>Take initiative and solve problems of moderate complexity</li>
<li>Demonstrate sound judgement in terms of handling complex, confidential, and regulated information</li>
<li>Lead both directly and by example</li>
</ul>
<ul>
<li>Preferred, but not required:</li>
<ul>
<li>At least 4 years of experience with clinical trial design and execution</li>
<li>At least 4 years of pharmaceutical industry experience </li>
<li>Experience with regulatory submissions and interactions</li>
</ul>
</ul>
Estimated compensation 170-190K/year USD DOE
Benefits
<ul>
<li>401(k) plan with company match </li>
<li>Medical, dental, and vision plans </li>
<li>Company-offered Life and Accidental Death &amp; Dismemberment (AD&amp;D) insurance </li>
<li>Company-provided short and long-term disability benefits </li>
<li>Unique offerings of Pet Insurance and Legal Insurance</li>
<li>Employee Assistance Program</li>
<li>Employee Discounts</li>
<li>Professional Development</li>
<li>Health Saving Account (HSA)</li>
<li>Flexible Spending Accounts</li>
<li>Various incentive compensation plans</li>
<li>Accident, Critical Illness, and Hospital Indemnity Insurance </li>
<li>Mental Health resources </li>
<li>Paid leave benefits for new parents </li>
</ul>
A note to recruiters:
We do not allow external search party solicitation. Presentation of candidates without written permission from the Ascendis Pharma Inc. Human Resources team (specifically from: Talent Acquisition Partner or Human Resources Director) is not allowed. If this occurs your ownership of these candidates will not be acknowledged.

Senior Clinical Scientist - Job ID: SCS

<h3>Job Description</h3>
Job DescriptionOur client a world leader in Pharmaceutical Research &amp; Development is seeking a Senior Clinical Science Specialist with ideally, experience in rare blood disorders.
<ul>
<li>Monitor patient eligibility, safety, and data and initiate appropriate action as appropriate</li>
<li>Ensure detail-oriented contributions are of high-quality and in compliance with regulatory requirements</li>
<li>Provide input in all stages of the clinical trial, from start-up to close-out</li>
<li>Scientifically support Clinical Development Phase 1, 2, 3; Data cleansing and analysis.</li>
</ul>
REQUIREMENTS
<ul>
<li>BA/BS</li>
<li>Advanced Clinical/Science Degree preferred (ei; PharmD, PhD, MSN, MPH)</li>
<li>2-5 years experience as Clinical Scientist</li>
<li>At least 4 years of Clinical Trial experience; Phase 1, 2, 3</li>
<li>Extensive experience with data analysis and review</li>
<li>Strong computer skills; Microsoft Office Suite (Word, PowerPoint and Excel), EDC RAVE, Spotfire </li>
<li>Occasional travel.</li>
</ul>
Relocation Assistance Available: Yes

1,445 Science Jobs