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Clinical Research Manager, Medical Affairs
Johnson & JohnsonManager, Clinical Research executing compliance strategies for R&D and Medical Affairs in a global role. Partnering with cross-functional teams to ensure adherence to regulations and ethical practices.
Posted 6/8/2026full-timeWest Chester • Massachusetts, New Jersey, New York, Pennsylvania • 🇺🇸 United StatesMid-LevelSeniorWebsite
About the role
Key responsibilities & impact- Provide strategic HCC leadership, oversight and execution of the G lobal Health Care Compliance program for R& D, Clinical Research, Medical Affairs, and related activities.
- Act as a compliance partner and trusted advisor to G lobal R&D, Clinical Research and Medical Affairs teams, providing timely , practical guidance on clinical trials, investigator and site interactions, advisory boards, and scientific exchange.
- Assist in identifying , assessing, and mitigating compliance risks associated with clinical research activities and medical engagement models.
- Support compliance risk assessments, issue management, and monitoring activities related to R&D, Clinical Research and Medical Affairs.
- Collaborate with Legal, Privacy, Quality, Finance, and other assurance functions to deliver coordinated compliance support and risk mitigation.
- Contribute to the development, implementation, and maintenance of policies, procedures, and training materials related to R&D, Clinical Research and Medical Affairs compliance.
- Support responses to internal inquiries, audits, monitoring activities, and regulatory requests related to clinical and medical compliance topics.
Requirements
What you’ll need- Bachelor’s degree in Law , Business, Compliance, Finance, Healthcare Administration, Life Sciences, or a related field
- 5–7 years of experience in healthcare compliance, clinical research operations, medical affairs, legal, audit, or related functions
- Working knowledge of healthcare compliance laws, regulations, and industry standards applicable to clinical research and medical affairs
- Experience supporting risk‑based compliance programs in regulated environments
- Strong analytical, problem‑solving, and decision‑making skills
- Effective written and verbal communication skills, with the ability to engage and influence stakeholders.
- Fluency in English required
Benefits
Comp & perks- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
healthcare complianceclinical research operationsmedical affairsrisk-based compliance programscompliance risk assessmentsissue managementmonitoring activitiespolicies and procedures developmenttraining materials developmentregulatory compliance
Soft Skills
analytical skillsproblem-solving skillsdecision-making skillswritten communicationverbal communicationstakeholder engagementinfluencing skills