Senior Clinical Trial Leader
Johnson & Johnson
19 days ago
Remote friendly (Palm Beach Gardens, FL)
United States
Clinical Research and Development
Senior Clinical Trial Leader (CTL)
About the Role
- Support planning and execution of one or more company-sponsored clinical trials within DePuy Synthes’ Clinical Operations, working with cross-functional colleagues, clinical sites, and external partners.
- Collaborate on clinical trial delivery focused on quality, compliance, and innovative medical device development.
Responsibilities
Clinical Trial Execution
- Serve as Clinical Trial Leader for assigned studies and participate on the clinical study core team.
- Support execution of company-sponsored medical device clinical trials (under appropriate supervision).
- Partner with Clinical Franchise colleagues and BSDMs to support study objectives.
- Ensure trials align with protocols, timelines, and regulatory requirements.
Operational Support & Collaboration
- Coordinate day-to-day study activities (site communication and vendor collaboration).
- Act as primary point of contact for sites; address operational challenges and escalate as appropriate.
- Track study budgets and support adherence to approved business plans.
- Assist with implementation of clinical systems, tools, and process improvements.
Communication, Compliance, Quality & Ethics
- Provide timely updates to internal stakeholders; support deliverables/publications.
- Support compliance with GCP, applicable regulations, and internal policies; follow HSE guidelines.
- Ensure efficient and responsible use of resources.
Required Qualifications
- Bachelor’s degree (or equivalent); preferred: Life Sciences, Physical Sciences, Nursing, or Biological Sciences.
- 2–4 years relevant experience with clinical research/clinical operations/regulatory environments.
Preferred Qualifications
- Clinical trial management or related roles; medical device development exposure.
- Clinical/healthcare background.
- Industry certifications (e.g., CCRA, RAC, CDE).
Benefits (time off)
- Vacation 120 hours/year; Sick time 40 hours/year (CO: 48; WA: 56); Holiday pay 13 days/year.
- Parental Leave 480 hours/year; Bereavement Leave; Caregiver Leave 80 hours; Volunteer Leave 32 hours; Military Spouse Time-Off 80 hours.
Application Instructions
- Apply via the company careers process.
About the Role
- Support planning and execution of one or more company-sponsored clinical trials within DePuy Synthes’ Clinical Operations, working with cross-functional colleagues, clinical sites, and external partners.
- Collaborate on clinical trial delivery focused on quality, compliance, and innovative medical device development.
Responsibilities
Clinical Trial Execution
- Serve as Clinical Trial Leader for assigned studies and participate on the clinical study core team.
- Support execution of company-sponsored medical device clinical trials (under appropriate supervision).
- Partner with Clinical Franchise colleagues and BSDMs to support study objectives.
- Ensure trials align with protocols, timelines, and regulatory requirements.
Operational Support & Collaboration
- Coordinate day-to-day study activities (site communication and vendor collaboration).
- Act as primary point of contact for sites; address operational challenges and escalate as appropriate.
- Track study budgets and support adherence to approved business plans.
- Assist with implementation of clinical systems, tools, and process improvements.
Communication, Compliance, Quality & Ethics
- Provide timely updates to internal stakeholders; support deliverables/publications.
- Support compliance with GCP, applicable regulations, and internal policies; follow HSE guidelines.
- Ensure efficient and responsible use of resources.
Required Qualifications
- Bachelor’s degree (or equivalent); preferred: Life Sciences, Physical Sciences, Nursing, or Biological Sciences.
- 2–4 years relevant experience with clinical research/clinical operations/regulatory environments.
Preferred Qualifications
- Clinical trial management or related roles; medical device development exposure.
- Clinical/healthcare background.
- Industry certifications (e.g., CCRA, RAC, CDE).
Benefits (time off)
- Vacation 120 hours/year; Sick time 40 hours/year (CO: 48; WA: 56); Holiday pay 13 days/year.
- Parental Leave 480 hours/year; Bereavement Leave; Caregiver Leave 80 hours; Volunteer Leave 32 hours; Military Spouse Time-Off 80 hours.
Application Instructions
- Apply via the company careers process.