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Clinical Affairs Jobs in Raleigh, NC (NOW HIRING)

Agilent

Clinical Affairs Scientist

Durham, NC · On-site +1

$105K - $197K/yr

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 ...

Danaher

Principal Clinical Scientist

Raleigh, NC · On-site +1

Partner crossfunctionally with R&D, Regulatory, Medical Affairs, Quality, and Commercial teams to align clinical programs with product development and market access needs. * Author and review ...

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Teleflex

Senior Commercial Product Manager

Morrisville, NC · On-site

$118K - $156K/yr

Leveraging your clinical background and healthcare expertise, you will serve as the bridge between clinicians, customers, Medical Affairs, Commercial teams, and Product Development to ensure that ...

Teleflex

Senior Commercial Product Manager

Morrisville, NC · On-site

$118K - $156K/yr

Leveraging your clinical background and healthcare expertise, you will serve as the bridge between clinicians, customers, Medical Affairs, Commercial teams, and Product Development to ensure that ...

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All JobsClinical Affairs JobsClinical Affairs Jobs in Raleigh, NC

Clinical Affairs information

See Raleigh, NC salary details

$21.4K

$121.8K

$200.2K

How much do clinical affairs jobs pay per year?

As of Aug 26, 2026, the average yearly pay for clinical affairs in Raleigh, NC is $121,785.00, according to ZipRecruiter salary data. Most workers in this role earn between $82,600.00 and $152,600.00 per year, depending on experience, location, and employer.

What is clinical affairs?

Clinical Affairs refers to the department or function within healthcare, medical device, or pharmaceutical organizations that manages clinical trials, regulatory compliance, and the collection of clinical data to support product approval and market access. Professionals in Clinical Affairs coordinate the planning, execution, and monitoring of clinical studies to ensure safety and efficacy standards are met. They also work closely with regulatory agencies to ensure all processes adhere to relevant laws and guidelines. This role is critical in bringing new medical products to market and maintaining ongoing compliance.

What are the key skills and qualifications needed to thrive in clinical affairs, and why are they important?

To thrive in Clinical Affairs, you need a strong background in life sciences or healthcare, regulatory knowledge, and experience managing clinical trials, often supported by a relevant degree or certification such as a CCRP or RAC. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and regulatory submission platforms is typical. Excellent organizational, problem-solving, and cross-functional communication skills set outstanding professionals apart in this field. These competencies are crucial for ensuring clinical studies are conducted ethically, efficiently, and in compliance with regulatory standards.

How does a clinical affairs professional typically collaborate with cross-functional teams during a clinical trial?

Clinical Affairs professionals work closely with regulatory, medical, and research teams throughout the lifecycle of a clinical trial. They are often responsible for ensuring that study protocols comply with regulatory requirements, coordinating with data management and biostatistics teams to monitor trial progress, and facilitating communication between investigators and sponsors. This role requires strong project management and interpersonal skills to align timelines, address challenges, and ensure the trial runs smoothly. Effective collaboration is essential for successful study outcomes and timely regulatory submissions.

What is the difference between Clinical Affairs vs Regulatory Affairs?

AspectClinical AffairsRegulatory Affairs
Required CredentialsTypically requires degrees in life sciences, clinical research certificationsRequires degrees in life sciences, regulatory certifications
Work EnvironmentHospitals, clinical research organizations, medical device companiesPharmaceutical, medical device, and biotech companies, regulatory agencies
Employer & Industry UsageFocuses on clinical trial management and patient safetyFocuses on compliance, submissions, and regulatory strategy

Clinical Affairs and Regulatory Affairs roles often overlap but serve different functions. Clinical Affairs manages clinical trials and patient safety, while Regulatory Affairs handles compliance and submissions to authorities. Both are essential in bringing medical products to market and require similar educational backgrounds.

What are the most commonly searched types of Clinical Affairs jobs in Raleigh, NC?

The most popular types of Clinical Affairs jobs in Raleigh, NC are:

What are popular job titles related to Clinical Affairs jobs in Raleigh, NC?

For Clinical Affairs jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Affairs jobs in Raleigh, NC look for?

The top searched job categories for Clinical Affairs jobs in Raleigh, NC are:

Clinical Affairs jobs near you
Infographic showing various Clinical Affairs job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 13% Part Time, and 7% Contract. Highlights an 84% Physical, 1% Hybrid, and 15% Remote job distribution, with an average salary of $121,785 per year, or $58.6 per hour.

Clinical Affairs Scientist

Agilent

Durham, NC • On-site, Remote

$105K - $197K/yr

Full-time

Posted 5 days ago

Agilent Technologies rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

50th of 544 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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