Regulatory & Clinical Affairs Manager Locations : Princeton, NJ (Onsite) (Full Time /Permanent) Note * FULLTIME Role and This role is on-site at Princeton, NJ The Role The Regulatory & Clinical ...
Regulatory & Clinical Affairs Manager Locations : Princeton, NJ (Onsite) (Full Time /Permanent) Note * FULLTIME Role and This role is on-site at Princeton, NJ The Role The Regulatory & Clinical ...
Clinical Affairs Manager (Southeast)
Atlanta, GA · On-site
$62K - $86K/yr
The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...
Clinical Affairs Manager (Southeast)
Atlanta, GA · On-site
$62K - $86K/yr
The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...
Clinical Affairs Manager (Southeast)
Atlanta, GA · On-site
$62K - $86K/yr
The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...
Clinical Affairs Manager (Southeast)
Atlanta, GA · On-site
$62K - $86K/yr
The Clinical Affairs Manager, Interventional Urology develops, manages, and delivers professional education to surgeons, OR staff, and sales representatives to achieve exceptional clinical outcomes ...
Clinical Affairs Manager
Pasadena, CA · On-site
... clinical affairs activities, and special projects Responsibilities: * Select Clinical consultants and Clinical Research Organizations (CROs) and manage their contracts * Recruit, hire, train, manage ...
Clinical Affairs Manager
Pasadena, CA · On-site
... clinical affairs activities, and special projects Responsibilities: * Select Clinical consultants and Clinical Research Organizations (CROs) and manage their contracts * Recruit, hire, train, manage ...
... clinical affairs activities, and special projects Responsibilities: * Select Clinical consultants and Clinical Research Organizations (CROs) and manage their contracts * Recruit, hire, train, manage ...
... clinical affairs activities, and special projects Responsibilities: * Select Clinical consultants and Clinical Research Organizations (CROs) and manage their contracts * Recruit, hire, train, manage ...
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
Quick apply
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
Regulatory Affairs Manager - IVD
San Diego, CA · On-site
$120 - $170/hr
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
Regulatory Affairs Manager - IVD
San Diego, CA · On-site
$120 - $170/hr
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
The position will work closely with R&D, Clinical Affairs, Quality, Manufacturing, Product Management, and external partners throughout the product development lifecycle. The ideal candidate has at ...
Clinical / Med Affairs Manager Summary (Scope of Job): The Clinical and Med Affairs Manager bridges the gap between clinical and commercialization needs of FLEX Vascular with responsibility of ...
Quick apply
Clinical / Med Affairs Manager Summary (Scope of Job): The Clinical and Med Affairs Manager bridges the gap between clinical and commercialization needs of FLEX Vascular with responsibility of ...
Clinical Affairs Associate
Norman, OK · Remote
Job Purpose The Clinical Affairs Associate supports the CARE team's evidence generation work by ... Study Monitoring & Data Management Support (as needed): Assist with or, as experience allows ...
Clinical Affairs Associate
Norman, OK · Remote
Job Purpose The Clinical Affairs Associate supports the CARE team's evidence generation work by ... Study Monitoring & Data Management Support (as needed): Assist with or, as experience allows ...
Clinical Affairs Associate
Norman, OK · On-site
Study Monitoring & Data Management Support (as needed): • Assist with or, as experience allows ... to the Clinical Affairs Lead. Post-Market Surveillance (PMS) Support: • Conduct ongoing ...
Clinical Affairs Associate
Norman, OK · On-site
Study Monitoring & Data Management Support (as needed): • Assist with or, as experience allows ... to the Clinical Affairs Lead. Post-Market Surveillance (PMS) Support: • Conduct ongoing ...
Director, Clinical Affairs
Pleasanton, CA · On-site
$89K - $121K/yr
The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Develop and manage study timelines, budgets, resource plans, enrollment forecasts, and key ...
Director, Clinical Affairs
Pleasanton, CA · On-site
$89K - $121K/yr
The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Develop and manage study timelines, budgets, resource plans, enrollment forecasts, and key ...
Director, Clinical Affairs
$89K - $121K/yr
The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Develop and manage study timelines, budgets, resource plans, enrollment forecasts, and key ...
Director, Clinical Affairs
$89K - $121K/yr
The Director, Clinical Affairs will serve as a key cross-functional leader and liaison among ... Develop and manage study timelines, budgets, resource plans, enrollment forecasts, and key ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
The Senior Project Manager, Clinical Affairs, plays a pivotal role in supporting Clinical Affairs activities by partnering with key functions and business units across the organization, including R&D ...
Clinical Affairs Manager information
See salary details
$63.5K - $72.7K
23% of jobs
$73.6K is the 25th percentile. Wages below this are outliers.
$72.7K - $81.9K
21% of jobs
The median wage is $87.4K / yr.
$81.9K - $91K
10% of jobs
$91K - $100.2K
0% of jobs
$100.2K - $109.4K
0% of jobs
$109.4K - $118.6K
3% of jobs
$118.6K - $127.8K
11% of jobs
$132.4K is the 75th percentile. Wages above this are outliers.
$127.8K - $137K
13% of jobs
$137K - $146.1K
8% of jobs
$146.1K - $155.3K
5% of jobs
$155.3K - $164.5K
5% of jobs
$63.5K
$106.2K
$164.5K
How much do clinical affairs manager jobs pay per year?
As of Aug 23, 2026, the average yearly pay for clinical affairs manager in the United States is $106,193.00, according to ZipRecruiter salary data. Most workers in this role earn between $75,500.00 and $135,000.00 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?
| Aspect | Clinical Affairs Manager | Clinical Research Associate |
|---|---|---|
| Required credentials | Bachelor's or higher in life sciences, often with certifications in clinical research | Bachelor's in life sciences, with certifications like CCRP or RAC often preferred |
| Work environment | Oversees clinical trials, manages teams, liaises with regulatory bodies | Monitors clinical trial sites, collects data, ensures protocol compliance |
| Employer and industry usage | Pharmaceutical, biotech, medical device companies, CROs | Research 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.
More about Clinical Affairs Manager jobs
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Cities with the most Clinical Affairs Manager job openings:
What are the most commonly searched types of Clinical Affairs jobs?
The most popular types of Clinical Affairs jobs are:
Who are the top companies hiring for Clinical Affairs Manager jobs?
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What states have the most Clinical Affairs Manager jobs?
States with the most job openings for Clinical Affairs Manager jobs include:
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Other
Posted 9 days ago
Job description
Role: Regulatory & Clinical Affairs Manager
Locations : Princeton, NJ (Onsite)
(Full Time /Permanent)
Note* FULLTIME Role and This role is on-site at Princeton, NJ
The Role
The Regulatory & Clinical Affairs Manager will play a key role in supporting the Company s regulatory and clinical initiatives across product development, regulatory submissions, and hospital collaborations.
This position is intended for a motivated professional seeking to grow into increasing levels of responsibility within a dynamic medical device environment. The successful candidate will be expected to independently manage assigned projects and develop well-reasoned regulatory recommendations, while working closely with cross-functional teams on overall regulatory and clinical strategy.
This role offers significant opportunities for professional growth, increased ownership, and direct exposure to executive-level strategic planning, regulatory agency interactions, and clinical partnerships.
The position combines regulatory affairs, clinical affairs, and hospital collaboration activities, supporting innovative AI-enabled medical imaging, surgical planning, surgical navigation, and digital health technologies.
Primary Responsibilities:
- Preparation and execution of regulatory submissions, including FDA 510(k) submissions, software modifications, and international registrations as applicable.
- Assess regulatory impact of software, AI/ML, cybersecurity, and product changes.
- Develop regulatory strategies and recommendations for new products and software upgrades.
- Support interactions with FDA, notified bodies, regulatory consultants, and international regulatory agencies.
- Monitor evolving regulatory requirements and communicate potential impacts to the organization.
- Support regulatory assessments related to design changes, risk management, verification, validation, and clinical evidence.
Qualifications:
- Bachelor s degree in engineering, Biomedical Engineering, Life Sciences, Regulatory Affairs, or related field.
- 5-12 years of experience in medical device regulatory affairs.
- Hands-on experience on FDA, CE, EU MDR submissions - candidates themselves shall still be active in preparing the submissions, rather than serving only in a managerial or oversight capacity
- Experience with Software as a Medical Device (SaMD)/SiMD, AI/ML-enabled medical devices, medical imaging, surgical navigation, robotics, or digital health products.
- Experience preparing and/or leading FDA 510(k) submissions.
- Experience supporting clinical studies, IRB submissions, or hospital-based research collaborations
- Familiarity with medical device quality systems and standards, including ISO 13485, ISO 14971, and IEC 62304.
- Experience with EU MDR and Technical Documentation submissions.
- Clinical affairs experience is a plnice to have