field_job_occupational_field_parents_all

field_job_employment_type

job_organization_name

city

state

<h3>Job Description</h3>
Job Description
POSITION SUMMARY:
Performs study-related clinical procedures according to the study protocol and provides care under appropriate supervision for subjects enrolled in clinical trials. Performs duties in accordance with ProSciento’s values, policies, and procedures.

DUTIES AND RESPONSIBILITIES:
<ul>
<li>Understands the main objectives of each ongoing study and the study procedures for which he/she will be responsible.</li>
</ul>
<ul>
<li>Demonstrates proficiency at performing basic clinical procedures such as vital signs, ECGs, phlebotomy, and sample processing.</li>
<li>Demonstrates proficiency in documenting observations and study procedures correctly and legibly in the source document.</li>
<li>Understands and demonstrates proficiency in appropriately responding to medical emergencies onsite.</li>
<li>Performs study procedures as assigned. </li>
<li>Observes and records data related to patient safety and study procedures.</li>
<li>Ensures that all study data is recorded accurately and completely. </li>
<li>Assists nursing staff and Clinical Project Managers with study procedures and patient management as directed.</li>
<li>Assists in the transcription of study data from source documents to Case Report Forms (CRFs)/ (eCRFs).</li>
<li>Understands and complies with Good Clinical Practices (GCPs), particularly those regarding the protection of human subjects and integrity of clinical trial data.</li>
<li>Understands and complies with ProSciento Standard Operating Procedures (SOPs) and Work Instructions (WIs).</li>
<li>Participates as requested in ProSciento Continuous Quality Improvement (CQI) process.</li>
<li>Flexibility to work mornings, evenings, and/or overnight shifts as needed.</li>
<li>Attends and participates in all required training activities.</li>
</ul>
<ul>
<li>Participates as requested as a Clinical Operations Study Liaison.</li>
<li>Assists with Screening Receptionist duties and responsibilities as requested.</li>
<li>Assists with Recruitment duties and responsibilities as requested.</li>
</ul>

 
JOB REQUIREMENTS / QUALIFICATIONS/EDUCATION:

Qualifications:
To perform this job successfully an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

Education and Experience:
High school diploma or general education degree (GED) as well as experience as a Medical Assistant, EMT, LVN, Phlebotomist, Foreign Medical Graduate (FMG), or Corpsman in a clinical or laboratory setting and/or equivalent combination of medical education, training, certifications, and/or experience. 

KNOWLEDGE, SKILLS, AND COMPETENCIES REQUIRED

Skills, Knowledge, and Abilities: 
Able to perform basic clinical procedures correctly including vital signs, ECGs, and sample processing. Demonstrates initiative and problem-solving skills. Able to respect subject confidentiality and blinding procedures. Understands medical terminology and calculations. Demonstrates a strong attention to detail with superior organizational skills. Under general supervision, exercises judgment in accordance with well-defined policies, procedures, and techniques. Able to self-monitor progress and complete assigned tasks independently. 

Competencies:
<ul>
<li>Functional/Technical Skills: Has the functional and technical knowledge and skills to do the job at a high level of accomplishment.</li>
<li>Peer Relationships: Can quickly find common ground and solve problems for the good of all; can represent his/her own interests and yet be fair to other groups; can solve problems with peers with a minimum of noise; is seen as a team player and is cooperative; easily gains trust and support of peers; encourages collaboration; can be candid with peers.</li>
<li>Process Management: Good at figuring out the processes necessary to get things done; knows how to organize people and activities; understands how to separate and combine tasks into efficient workflow; knows what to measure and how to measure it; can see opportunities for synergy and integration where others can’t; can simplify complex processes; gets more out of fewer resources.</li>
<li>Action Oriented: Enjoys working hard; is action oriented and full of energy for the things he/she sees as challenging; not fearful of acting with a minimum of planning; seizes more opportunities than others.</li>
<li>Time Management: Uses his/her time effectively and efficiently; values time; concentrates his/her efforts on the more important priorities; gets more done in less time than others; can attend a broader range of activities.</li>
</ul>
Certificates and Licenses:
<ul>
<li>Basic Life Support (BLS) certification is required and may be provided by the company. GCP training is required and will be provided by the company.</li>
</ul>
Language Skills:
<ul>
<li>Must be proficient in both verbal and written English. Able to communicate effectively with both employees and management. Ability to read and interpret documents such as safety rules, WIs, SOPs, medical terminology, and procedure manuals. </li>
</ul>
Math Skills:
<ul>
<li>Able to add, subtract, multiply, and divide in all units of measure using whole numbers, fractions and decimals. Able to compute rate, ratio, and percent and to draw and interpret bar graphs.</li>
</ul>

Reasoning Skills: 
<ul>
<li>Ability to apply common sense understanding to carry out instructions provided in written, oral or diagram form. Ability to deal with problems involving several concrete variables in standardized situations.</li>
</ul>
Computer Skills: 
<ul>
<li>To perform this job successfully an individual should have excellent computer skills with working knowledge in the current Microsoft Office Suite as well as Microsoft Windows operating systems. </li>
</ul>
 This position requires open availability for shift scheduling, including the ability to work any of the following shifts on an as-needed basis: 1st Shift (Day) ,2nd Shift (Evening), 3rd Shift (Overnight). Candidates must also be available to work weekends and holidays, as coverage during these times may be required to meet operational needs. This role is a part-time, non-benefited role.

Research Assistant

<h3>Job Description</h3>
Job DescriptionSenior Scientist, Potency Assay Location: San Diego, CA Employment Type: Full-time Hiring Company: BioPhase (on behalf of our client) Pay: $145,000–$165,000 base + bonus; stock options Hours: Monday–Friday, full-time Job Description: We’re seeking a Senior Scientist to develop and qualify target-binding and cell-based potency assays for protein biologics and conjugates. You’ll own assay strategy from discovery through CMC, and lead method transfer/implementation at CDMOs for lot release, stability, and characterization in support of clinical manufacturing. Essential Duties and Responsibilities: • Build GMP QC-compatible target engagement and cell-based potency assays for multiple modalities. • Culture/maintain cell lines and create well-documented cell banks for assay use. • Identify, qualify, and manage critical reagents; maintain assay readiness. • Author/review development reports, method transfer/verification/qualification protocols, and summaries. • Review GMP release/stability results; support OOS/OOT investigations, QC data review, and batch release at partner sites. • Partner with CDMOs on reference standard qualification and assay lifecycle management. • Collaborate cross-functionally to advance programs from discovery to CMC. Qualifications: • MS/PhD in Biology, Biochemistry, or related field. • 5+ years’ industry experience developing potency assays. • Hands-on expertise qualifying recombinant and cell-based assays (target binding, signaling, cytotoxicity) for GMP use. • Proficient with data analysis tools (e.g., GraphPad Prism, SoftMax Pro). • Strong communicator; effective with internal teams and external CDMOs. Preferred: • Prior CDMO collaboration and exposure to regulatory filings. • Experience with process-related impurity testing (bioburden, HCP, residual DNA, leached Protein A). Benefits: Comprehensive package including medical, dental, vision, life &amp; disability insurance; 401(k); FSA; EAP; PTO &amp; parental leave; flexible schedule; relocation assistance; year-end shutdown. Apply today and join our team!

Sr. Scientist, Potency Assay

<h3>Job Description</h3>
Job Description
We have immediate opportunities for Senior Fisheries Biologists for the Southern California area.
Duties and Responsibilities
<ul>
<li>Ability to lead, manage and execute fisheries and aquatic resource-related studies, including design and implementation of fisheries assessments, habitat assessments, fish population analyses, fish passage assessments, instream flow studies, benthic macroinvertebrate bioassessments, and aquatic restoration efforts.</li>
<li>This person will also oversee fisheries and aquatic resource data analyses and provide quality assurance/quality control.</li>
<li>Other responsibilities may include building and maintaining client relations, leading pursuits of upcoming project work, preparation of scopes and budgets, strategic planning, and mentoring/supervising junior and mid-level staff.</li>
</ul>
Educations and Qualifications
<ul>
<li>Bachelor's degree plus 10 years’ experience or Master’s or PHD with a minimum of seven years of experience.</li>
<li>Candidates should be well-versed in issues related to coastal/marine, aquatic ecology with strong knowledge and experience with projects involving freshwater and anadromous fish species, as well as preparation of CEQA, NEPA, and ESA/CESA compliance documents. Knowledge and experience with FERC processes is also desired.</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(FERC, CEQA, NEPA, ESA/CESA, Biologist, Fisheries, Aquatic Restoration, Fish, Habitat)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Senior Fisheries Biologist

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a Senior Archaeologist for various offices throughout California. This ideal candidate will be responsible for mentoring and leading a team of archeologists on field and laboratory work.
Job Responsibilities include, but are not limited to:
<ul>
<li>Providing mentorship and leadership to mid-level and junior staff</li>
<li>Coordinating project tasks to meet cost and schedule objectives</li>
<li>Supervising and participating in field and laboratory work</li>
<li>Supervising groups of Senior, Staff, Associate, and Assistant Archaeologists</li>
<li>Authoring cultural resources technical reports</li>
<li>Developing new business from referrals from new and/or existing clients and assisting with marketing efforts</li>
<li>Preparing cultural resources proposals and assisting with the preparation of multidisciplinary proposals</li>
<li>Assisting the Group Manager and/or Department Director with review of department staff members</li>
<li>Serving as a tribal liaison</li>
<li>Training staff in cultural resource project/task completion and reviewing work of other team members</li>
</ul>
Education and Experience Required:
<ul>
<li>Master’s or doctorate degree in Anthropology or Archaeology</li>
<li>Minimum of 10 plus years of experience in environmental and cultural resources management consulting in California</li>
<li>Registered Professional Archaeologist (or ability to become certified as such immediately upon hire)</li>
<li>Must have the ability/willingness to carry out fieldwork and/or construction monitoring when needed, which may require periodic travel and work in extreme or challenging physical environments</li>
<li>Strong working knowledge of the federal and state regulatory settings</li>
<li>Proven ability to author cultural resource management reports</li>
<li>Knowledge of the prehistory, history, archaeology, and ethnography of California</li>
<li>Has demonstrated experience serving as a consultant in an advisory capacity to clients</li>
<li>Project Management experience including a proven ability to be on time and on budget</li>
<li>Excellent problem-solving skills</li>
<li>Effective writing and oral communication skills including presentations</li>
<li>Strong organizational skills and work ethic</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
Cultural Resources, Archaeologist, Anthropologist, Anthropology, technical reports, prehistorical, Registered Professional
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Archaeologist - Senior

<h3>Job Description</h3>
Job DescriptionAssociate Assay Development Scientist Are you looking for your next career opportunity? CellCarta, a leading integrated pathology laboratory and global contract research organization, is seeking a full-time&nbsp;Associate Assay Development Scientist.&nbsp;Come work with a team of talented individuals who are committed to making a positive impact on human health and well-being. Apply today and take the first step towards an exciting new career with CellCarta! Summary The Associate Assay Development Scientist is responsible for providing support to the Assay Development team across all stages of a study, from start-up to data reporting, and for coordinating with internal teams and stakeholders to ensure clear and timely completion of study deliverables. The individual will also be responsible for assisting with operational Responsibilities
<ul>
<li>Provide support to the Assay Development team with administrative-level study activities such as study initiation, laboratory scheduling, project tracker updates, specification worksheet preparation, image uploads, scheduling data analysis and data transcription/QC, and release of data spreadsheets to clients.</li>
<li>Coordinate with internal teams, including members of the Laboratory, Digital Pathology, Pathology, Pathology Support, Operations, Biosample Management, Procurement, IT, QA and Project Management teams to coordinate the completion of study activities within the predetermined timelines.</li>
<li>Proactively address potential issues, provide updates and collaborate effectively to achieve project-specific goals.</li>
<li>Submit study updates monthly to management.</li>
<li>Assist with monthly revenue recognition activities.</li>
<li>Assist in maintenance/inventory of the tissue bank and with tissue sample procurement.</li>
<li>Initiate and QC review new specification worksheets.</li>
<li>Initiate and QC review new autostainer protocols.</li>
<li>Assist with tracking and managing all staining protocols and versions.</li>
<li>Coordinate and assist with assay transfers between CellCarta laboratories.</li>
<li>Provide feedback to management regarding challenges relating to laboratory and assay development.</li>
<li>Perform clinical, non-clinical, and internal research projects approved by CellCarta Management or the Medical Director.</li>
<li>Maintain detailed and accurate records of all assays and results.</li>
<li>Responsible for other duties as assigned by manager.</li>
</ul>
Education
<ul>
<li>Bachelor’s degree in medical technical, clinical laboratory, chemical, physical or biological science; or associate degree in chemical, physical or biological science or medical laboratory or equivalent education and training is preferred.</li>
</ul>
Qualifications
<ul>
<li>Experience in a histology laboratory with basic knowledge of histology techniques. Qualifications to perform moderate or high-complexity clinical sample testing or inclusion criteria testing for clinical trials is a plus.</li>
<li>Knowledge of GCP, GCLP, GLP guidelines.</li>
<li>Good communication skills.</li>
<li>Detail-oriented with demonstrated analytical thinking and problem-solving skills.</li>
<li>Strong organizational skills, timeliness and the ability to prioritize tasks effectively.</li>
<li>Proactive attitude with an eagerness to learn and adapt.</li>
<li>Ability to read and interpret documents such as protocols, safety rules, and procedure manuals written in English. Ability to record results in English.</li>
<li>Ability to solve practical problems and to interpret a variety of instructions furnished in written, oral or schedule form. </li>
</ul>
Working Conditions
<ul>
<li>40 hours per week, Monday – Friday, 9am - 5pm</li>
</ul>
What we can offer CellCarta is made up of dedicated professionals who are focused on achieving our mission of impacting the future of patient therapy. We make a difference in the lives of patients around the world! We offer a wide range of benefits including:
<ul>
<li>Competitive wages:&nbsp;$65,000 to $80,000</li>
<li>Medical, dental, and vision benefits</li>
<li>401k retirement savings plan with a healthy match</li>
<li>Vacation and sick time</li>
<li>Employee Assistance Program</li>
<li>Career development opportunities</li>
<li>Continuing education</li>
</ul>
About Us CellCarta is a rapidly growing, stable company. We are a leading provider of pre-clinical and clinical trial services to pharmaceutical and biotechnology companies. Our laboratory service offerings include immunohistochemistry, FISH, CTC isolation and characterization, chemosensitivity testing, tissue procurement, flow cytometry, ELISA, mutation testing, cell expansion, and colony-forming assays. CellCarta is a CLIA-licensed and CAP-accredited laboratory, and we perform studies in compliance with the relevant portions of Good Laboratory and Good Clinical Practices. Join us as we make an impact on the future of patient therapy! Supplemental Information Candidates must be legally authorized to work in the United States on a permanent basis. Verification of employment eligibility will be required at the time of hire. Visa sponsorship is not available.
The information collected to review your application will be processed by the human resources services of CellCarta Biosciences Inc. and its affiliates (collectively, “CellCarta”). The legal basis for this processing is the legitimate interest of CellCarta to evaluate the suitability of candidates for the roles available at CellCarta.
CellCarta will only process that information which is necessary to evaluate your application. This information includes identifying information such as your name, address, email address and phone number, as well as information about your education and professional experience, including previous positions and your CV. Such information is required for us to complete your applicant file, assess your suitability for the role and comply with applicable laws. CellCarta may obtain personal information from other sources, such as during reference, background, or employment checks, with your permission, and from third party sources such as recruitment and assessment sites or professional social media sites, in each case only if such information is relevant to reviewing your application. Your personal information will be retained only for so long as reasonably necessary and in accordance with applicable laws. This information will be processed confidentially and only accessed by those who have a need for the recruitment process. Please note that the information comprising your applicant file may be processed in a country that is not where you are located (for example, you might be in the European Economic Area or Québec, Canada, whereas your applicant file may be reviewed by CellCarta in the United States). If you are offered and accept employment with CellCarta Biosciences Inc. or one of its affiliates, the information collected will become part of your employment record. If you do not want us to retain your information, or want us to update it, please contact&nbsp;<a href="mailto:privacy@cellcarta.com" target="_blank">privacy@cellcarta.com</a>.
 &nbsp;
Powered by JazzHR
LfqiqNhBSj

Associate Assay Development Scientist

<h3>Job Description</h3>
Job Description
We have an immediate need for a Paleontologist. This is an On-call position working on projects throughout California. This individual will be responsible for conducting paleontological monitoring of construction projects to include data collecting, interpretation of stratigraphic units, and salvaging of fossils.
Qualifications
<ul>
<li>BS or BA degree in Geology or Paleontology and one year experience monitoring in the state or geologic province of the specific project AS or AA in Geology, Paleontology, or Biology and demonstrated two years’ experience collecting and salvaging fossil materials in the state or geologic province of the specific project.</li>
<li>Ability to identify vertebrate, invertebrate, plant, and trace fossils to class or lower taxonomic level in the field is desirable</li>
<li>Ability to travel</li>
</ul>
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Paleontologist, Geology, Monitoring, Fossils, Geologic Province, Plants, Biology)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Paleontologist

<h3>Job Description</h3>
Job Description
We have immediate opportunity for all levels of Wildlife Biological Monitors for the Central Valley Area. MUST have Wildlife Biological Monitoring Experience in California.
VARIOUS DUTIES AND RESPONSIBILITIES (other duties may be assigned)
<ul>
<li>Experience and knowledge of wildlife species in the Central Valley including small mammals, birds, and reptiles.</li>
<li>Familiarity with state and federal regulations, knowledge of environmental regulatory process is a must.</li>
<li>Experience with monitoring all ground distributing activity including mass grading, grubbing, weed abatement, trenching and any excavation on previously disturbed and undisturbed ground.</li>
<li>Does or oversees field inspections of proposed project areas.</li>
<li>Perform biological monitoring at construction sites to implement mitigation measures.</li>
<li>Conduct field surveys.</li>
<li>Record data for scientific and compliance purposes using company forms and established field methodology.</li>
<li>Ability to read maps.</li>
<li>Prepare daily progress/monitoring reports as needed by the project.</li>
<li>Use GPS equipment (Garmin/Trimble) for field data collection.</li>
<li>Ability to travel to be in the field for extended periods and able to work in rough terrain and challenging weather inclement.</li>
<li>Work independently or as part of a team.</li>
</ul>
VARIOUS DEGREES &amp; SKILLS
<ul>
<li>Master’s or Bachelor’s Degree in Biology or closely related field.</li>
<li>Previous construction monitoring experience in similar California environments.</li>
<li>Knowledge of local, state, and federal environmental regulations.</li>
<li>Team player with the ability to work in a fast-paced environment.</li>
<li>Sound business ethics, including the protection of proprietary and confidential information.</li>
<li>Proficiency in MS Office Applications (Word, PowerPoint, Outlook, Excel) and project tracking software and databases.</li>
<li>Experience with any of the following species: Tipton Kangaroo Rat, San Joaquin Antelope Squirrel, California Tiger Salamander, San Joaquin Kit Fox, Giant Garter Snake</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Biologists, Biology, GPS, endangered species, field surveys, mammal, amphibian)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Wildlife Biologist

<h3>Job Description</h3>
Job Description
We have an immediate opportunity for a full-time architectural historian in the Northern California area. This position will require fieldwork.
Job Responsibilities
<ul>
<li>Conducting archival research</li>
<li>Prepare historic context, applying National Register criteria.</li>
<li>Prepare architectural history components of NHPA and CEQA technical reports</li>
<li>Document Architectural resources on California DPR 523 records and History American Building Survey (HABS) / Historic American Engineering Record (HAER) / Historic American Landscape Survey (HALS), and other duties as assigned</li>
<li>Excellent written and oral communication</li>
<li>Knowledge of GIS and basic understanding of cultural resources mapping and date collection</li>
<li>Previous field experience</li>
<li>Travel within Northern California as required</li>
</ul>
Education and Experience
<ul>
<li>Master of Arts (evidence of completion or nearly completed) in Historic Preservation, Public History, Architecture, Architectural History or closely related</li>
<li>1-2 years of experience</li>
<li>Proficiency with Microsoft Suite</li>
</ul>
We offer a generous benefits package including company-paid medical insurance, paid holidays, 401k and paid time off (PTO)
Upon a conditional job offer, a drug test and background check will be required.
Compensation based on experience.
(Architectural, Historian, GIS, Historic Preservation, Cultural Resources, CEQA, NHPA)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

Architectural Historian

<h3>Job Description</h3>
Job Description
We have several opportunities for on-call Field Archaeologists to monitor for a project located in the Ontario area.
· Willing to work 6:30 am to approximately 3:30 pm (1 to 4 days per week for the next 3 weeks or longer).
· Willing to work on Saturdays if needed.
· Have a BA or higher degree in Archaeology/Anthropology.
· Have around 2 years’ experience in CRM, monitoring experience desired.
(Archaeologist, anthropologist, archaeology, anthropology, CRM, cultural resources management)
Company DescriptionAbout us: 347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>. 
<h3>Company Description</h3>
About us:\r\n\r\n347 Group, Inc. provides staffing resources to a variety of industries. We have an experienced team of staffing professionals and provide a wide range of services to our clients. Visit our website <a href="http://www.347group.com" target="_blank">www.347group.com</a>.

On Call Field Archaeologist

<h3>Job Description</h3>
Job DescriptionAbout Workato
Workato transforms technology complexity into business opportunity. As the leader in enterprise orchestration, Workato helps businesses globally streamline operations by connecting data, processes, applications, and experiences. Its AI-powered platform enables teams to navigate complex workflows in real-time, driving efficiency and agility.
Trusted by a community of 400,000 global customers, Workato empowers organizations of every size to unlock new value and lead in today's fast-changing world. Learn how Workato helps businesses of all sizes achieve more at workato.com.
Why join us?
Ultimately, Workato believes in fostering a flexible, trust-oriented culture that empowers everyone to take full ownership of their roles. We are driven by innovation and looking for team players who want to actively build our company. 
But, we also believe in balancing productivity with self-care. That's why we offer all of our employees a vibrant and dynamic work environment along with a multitude of benefits they can enjoy inside and outside of their work lives. 
If this sounds right up your alley, please submit an application. We look forward to getting to know you!
Also, feel free to check out why:
<ul>
<li>
Business Insider named us an "enterprise startup to bet your career on"
</li>
<li>
Forbes' Cloud 100 recognized us as one of the top 100 private cloud companies in the world
</li>
<li>
Deloitte Tech Fast 500 ranked us as the 17th fastest growing tech company in the Bay Area, and 96th in North America
</li>
<li>
Quartz ranked us the #1 best company for remote workers
</li>
</ul>
Responsibilities
We are looking for an exceptional AI Research Scientist to join our growing team. In this role, you will be responsible to:
<ul>
<li>
Explore workflow‑aware planning, cost‑optimised RAG, tool‑use evaluation, and multi‑agent collaboration.
</li>
<li>
Prototype and benchmark models; present findings internally and externally.
</li>
<li>
Collaborate with Product &amp; Engineering to ship research‑backed features.
</li>
<li>
Contribute to open‑source repos and author technical blogs.
</li>
</ul>
Requirements
Qualifications / Experience / Technical Skills
<ul>
<li>
MS/PhD in Computer Science, ML, or related field—or equivalent experience.
</li>
<li>
Hands‑on with PyTorch/JAX and modern LLM frameworks.
</li>
<li>
Strong publication record in top-tier ML venues (NeurIPS, ICML, ICLR) or demonstrable impactful experimental work; hands‑on experience with large‑scale model training, transformer architectures, reinforcement‑learning techniques, and CUDA.
</li>
</ul>
Soft Skills / Personal Characteristics
<ul>
<li>
Curiosity‑driven and self‑directed.
</li>
<li>
Ability to explain complex ideas to non‑experts.
</li>
<li>
Team player who welcomes feedback and knowledge‑sharing.
</li>
</ul>
(REQ ID: 2124)

1,364 Science Jobs