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Clinical Affairs In Usa Jobs (NOW HIRING)

Agilent

Clinical Affairs Scientist

Philadelphia, PA · On-site +1

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical ... The ideal candidate will have a strong background in clinical science/research and experience ...

Agilent

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical ... The ideal candidate will have a strong background in clinical science/research and experience ...

Agilent

Clinical Affairs Scientist

Carpinteria, CA · On-site

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical ... The ideal candidate will have a strong background in clinical science/research and experience ...

Saluda Medical

$180 - $280/hr

In this exciting role as a Director, Clinical Affairs, you will be at the center of Saluda's clinical study program. Your insights will contribute to formulating the clinical research and evidence ...

Agilent

Clinical Affairs Scientist

Wood Dale, IL · On-site +1

$105K - $197K/yr

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical ... The ideal candidate will have a strong background in clinical science/research and experience ...

Phia LLC

Senior Clinical Affairs manager

Indiana, PA · On-site

$161.09 - $223.05/hr

Do you bring a strong background in clinical affairs, clinical science, or clinical operations within IVD or molecular diagnostics? Have you designed clinical performance studies and shaped clinical ...

BioTalent

Director Clinical Affairs

San Mateo, CA · On-site

$170K - $225K/yr

Director of Clinical Affairs We're seeking a Director of Clinical Affairs to own end-to-end ... Develop study design from scratch in close collaboration with internal management, regulatory ...

BioTalent

Director Clinical Affairs

Hayward, CA · On-site

$172K - $227K/yr

Director of Clinical Affairs We're seeking a Director of Clinical Affairs to own end-to-end ... Develop study design from scratch in close collaboration with internal management, regulatory ...

BioTalent

Director Clinical Affairs

Fremont, CA · On-site

$164K - $216K/yr

Director of Clinical Affairs We're seeking a Director of Clinical Affairs to own end-to-end ... Develop study design from scratch in close collaboration with internal management, regulatory ...

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$22K

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How much do clinical affairs in usa jobs pay per year?

As of Sep 5, 2026, the average yearly pay for clinical affairs in usa in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Affairs In Usa vs Clinical Research Associate?

AspectClinical Affairs In UsaClinical Research Associate
Required CredentialsTypically requires a degree in life sciences, nursing, or related field; certifications like CCRP or RAC are commonOften requires a degree in life sciences; certifications like CCRP are advantageous
Work EnvironmentWorks within pharmaceutical or biotech companies, overseeing clinical trial processes and complianceWorks on-site or remotely, monitoring clinical trial sites and ensuring protocol adherence
Employer & Industry UsageUsed mainly in pharmaceutical, biotech, and medical device industries in the USCommonly employed by CROs, pharmaceutical companies, and research institutions

While both roles involve clinical trial processes, Clinical Affairs In Usa focuses on regulatory compliance, strategy, and overall clinical program management, whereas Clinical Research Associates primarily monitor and coordinate trial sites to ensure protocol adherence. Both roles require similar credentials and are integral to the clinical research industry in the US.

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Clinical Affairs In Usa jobs near you
Infographic showing various Clinical Affairs In Usa job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Clinical Affairs Scientist

Agilent

Philadelphia, PA • On-site, Remote

$105K - $197K/yr

Full-time

Posted 16 days ago

Key responsibilities

  • Support clinical trial study designs and execution, including authoring study protocols and reports.

  • Collaborate with cross-functional teams and external partners to generate clinical evidence and ensure compliance.

  • Provide scientific oversight and contribute to regulatory submissions, scientific publications, and marketing materials.

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer(OCMO) Global Clinical Affairs team. The CAS' main responsibilities will be to support clinical evidence generation, in conjunction with cross-functional teams as part of the co-development process of companion diagnostics in the field of oncology. This position will support clinical trial study designs and execution, regulatory applications, and scientific marketing deliverables. The ideal candidate will have a strong background in clinical science/research and experience working in pharmaceutical, biomarker, and/or in vitro diagnostic clinical development. The candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. This position reports to the Manager of Clinical Affairs Sciences and has no direct reports.
Responsibilities include but are not limited to:

  • Provide thought leadership on key relevant clinical topics to support strategy development and execution.

  • Generation of content to support external validation studies including study design and authoring of study protocols and reports. May also contribute to cutoff/cutpoint determination studies, method comparison, bridging, and analytical concordance studies.

  • Design and develop databases, Electronic Data Capture (EDC) systems, and case report forms.

  • Contribute to risk analyses, study quality control activities, and instream data monitoring in clinical trials.

  • Ensure scientific validity of reported results including statistical analysis, tabulation, and presentation of data.

  • Collaborate with regulatory and development teams during the submission process including authoring of clinical performance information and other documentation such as Instructions for Use (IFU).

  • Provide clinical and scientific oversight of local marketing and commercial materials.

  • Ensure effective, efficient and compliant Clinical Affairs processes including preparing, revising, and maintaining standard operating procedures for the conduct of clinical studies.

  • Serve as the clinical science subject matter expert in cross-functional internal meetings as well as meetings with pharmaceutical partners and regulatory bodies.

  • Author manuscripts, abstracts, whitepapers and prepare oral/poster presentations.

  • Support audits and inspections as a clinical subject matter expert.

Qualifications

  • Master's degree or advanced degree (e.g., Ph.D., Pharm. D., M.D.) in pharmaceutical, medical or relevant biomedical science fields. Advanced Degree preferred.

  • 4+ years of experience in IVD product development, clinical research, medical writing, and/or clinical science in the medical device and/or pharmaceutical industry.

  • Familiarity with clinical trial design, conduct, and oversight including biostatistics, and Good Clinical Practice preferred.

  • Ability to interpret regulatory standards, guidance, and laws.

  • Strong scientific, medical writing, and presentation skills

  • Exceptional ability to manage multiple projects in a fast-paced environment with changing priorities.

  • Must be able to work and make independent decisions, understand complex scientific and clinical data information, and be able to take the initiative to lead projects and assignments.

  • Experience working with external partners and/or regulatory bodies including the FDA.

  • Knowledge in oncology, immunology, and/or pathology preferred.

Additional Details

This job has a full time weekly schedule. It includes the option to work remotely. Applications for this job will be accepted until at least August 27, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $105,280.00 - $197,400.00/yr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Medical/Clinical

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