ZipRecruiter

Log In

1

Clinical Affairs Manager Jobs in Raleigh, NC (NOW HIRING)

Agilent

Clinical Affairs Scientist

Durham, NC · On-site +1

$105K - $197K/yr

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 ...

Bioventus LLC

Regulatory Affairs Manager

Durham, NC · On-site

$90 - $120/hr

Regulatory Affairs Manager Bioventus is a global leader in developing clinically proven, cost‑effective solutions for pain treatment, joint preservation, restorative therapies, and bone graft ...

Osv_bioventus

Regulatory Affairs Manager

Durham, NC · On-site

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... and Operations, Clinical/Medical Affairs, and other functional areas to provide regulatory ...

Osv_bioventus

Regulatory Affairs Manager

Durham, NC · On-site

The Regulatory Affairs Manager is responsible for developing and executing global regulatory ... and Operations, Clinical/Medical Affairs, and other functional areas to provide regulatory ...

Teleflex

Senior Commercial Product Manager

Morrisville, NC · On-site

$118K - $156K/yr

... Manager - Clinical Initiatives , you will have a unique opportunity to lead strategic clinical ... Partner with Clinical Affairs, Medical Affairs, and KOLs to identify evidence gaps and support ...

Teleflex

Senior Commercial Product Manager

Morrisville, NC · On-site

$118K - $156K/yr

... Manager - Clinical Initiatives , you will have a unique opportunity to lead strategic clinical ... Partner with Clinical Affairs, Medical Affairs, and KOLs to identify evidence gaps and support ...

next page

Showing results 1-20

All JobsClinical Affairs JobsClinical Affairs Manager JobsClinical Affairs Manager Jobs in Raleigh, NC

Clinical Affairs Manager information

See Raleigh, NC salary details

$56.1K

$93.8K

$145.2K

How much do clinical affairs manager jobs pay per year?

As of Aug 27, 2026, the average yearly pay for clinical affairs manager in Raleigh, NC is $93,759.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,700.00 and $119,200.00 per year, depending on experience, location, and employer.

What does a clinical affairs manager do?

A Clinical Affairs Manager oversees the planning, execution, and management of clinical trials for medical devices, pharmaceuticals, or biotechnology products. They ensure studies comply with regulatory requirements, manage budgets and timelines, and coordinate with cross-functional teams such as regulatory, medical, and research staff. Their role is crucial in generating clinical evidence necessary for product approvals and post-market surveillance. Effective communication and strong organizational skills are essential for success in this position.

What are the key skills and qualifications needed to thrive as a clinical affairs manager?

To thrive as a Clinical Affairs Manager, you need a strong background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) guidelines, and regulatory submission processes such as FDA or EMA requirements is crucial. Exceptional leadership, problem-solving, and communication skills help you coordinate teams and manage complex projects effectively. These competencies are vital for ensuring regulatory adherence, advancing clinical studies, and supporting successful product development in healthcare organizations.

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

A Clinical Affairs Manager works closely with cross-functional teams such as regulatory affairs, research and development, quality assurance, and marketing throughout the lifecycle of a clinical trial. They coordinate with these teams to ensure that clinical studies are designed, conducted, and reported in compliance with regulatory requirements and company goals. Regular meetings, clear communication, and effective project management are essential to align timelines, manage resources, and address any challenges that arise. This collaborative environment helps ensure that clinical evidence supports product claims and market approval.

What is the difference between Clinical Affairs Manager vs Clinical Research Associate?

AspectClinical Affairs ManagerClinical Research Associate
Required credentialsBachelor's or higher in life sciences, often with certifications in clinical researchBachelor's in life sciences, with certifications like CCRP or RAC often preferred
Work environmentOversees clinical trials, manages teams, liaises with regulatory bodiesMonitors clinical trial sites, collects data, ensures protocol compliance
Employer and industry usagePharmaceutical, biotech, medical device companies, CROsResearch sites, CROs, pharmaceutical companies

The Clinical Affairs Manager focuses on overseeing clinical trial operations, regulatory compliance, and team management, while the Clinical Research Associate primarily monitors trial sites and ensures protocol adherence. Both roles require similar educational backgrounds and certifications but differ in scope and responsibilities within the clinical research process.

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 Manager jobs in Raleigh, NC?

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

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

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

What cities near Raleigh, NC are hiring for Clinical Affairs Manager jobs?

Cities near Raleigh, NC with the most Clinical Affairs Manager job openings:

Clinical Affairs Manager jobs near you
Infographic showing various Clinical Affairs Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 81% Full Time, 8% Part Time, and 11% Contract. Highlights an 90% In-person, and 10% Remote job distribution, with an average salary of $103,222 per year, or $49.6 per hour.

Clinical Affairs Scientist

Durham, NC • On-site, Remote

Agilent
Biotechnology Research and Development • 10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

50th of 544 rated manufacturers

People enjoy working here

Good employer

Recommended by parents

Learn more about Agilentexternal

$105K - $197K/yr

Full-time

Posted 6 days ago

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

What Agilent Technologies employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply