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Johnson & Johnson

Clinical Research Manager, Medical Affairs

Johnson & Johnson

Manager, 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

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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