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Associate Clinical Research Associate – Site Manager
Johnson & JohnsonAssociate Clinical Research Associate role focused on site management and compliance at Johnson & Johnson. Involves supporting clinical trials and ensuring adherence to protocols.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial monitoring, site initiation, and compliance with GCP and local regulations. Proficient in managing site-level activities, training staff, and contributing to recruitment strategies while ensuring accurate data collection and financial tracking.
Highest-signal resume keywords
Clinical Trial Monitoring ExperienceGCP KnowledgeSite Initiation and Start-UpAI LiteracyMultilingual Proficiency
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial MonitoringSite InitiationData ComplianceCost TrackingRecruitment Strategy
Soft Skills
Training and DevelopmentContingency Planning
Tools & Technologies
Clinical Trial Management SystemsIT Software Proficiency
Industry Keywords
PharmacyNursingLife SciencesGCPSOPsLocal Laws and Regulations
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Acts as primary local company contact for assigned sites for specific trials
- Participates in site feasibility and/or Site Qualification Visit
- Responsible for executing activities within site initiation and start-up
- Ensures site staff are trained and the corresponding training records are complete and accurate
- Contributes to site level recruitment strategy and contingency planning
- Ensures that clinical drug supplies are appropriately used, handled, and stored
- Ensures compliance with all data collected
- Tracks costs at site level and ensure payments are made
Requirements
What you’ll need- A minimum of a BA or BS degree in Pharmacy, Nursing, Life Sciences, or related scientific field (or equivalent experience)
- A minimum of 1 year of clinical trial monitoring experience is required
- Demonstrated AI literacy and an AI enabled mindset
- Basic working knowledge of GCP, company SOPs, local laws, and regulations
- Strong IT skills in appropriate software and company systems
- Proficient in speaking English, Dutch and French for candidates based in Belgium
- Proficient in speaking English, and Dutch for candidates based in the Netherlands
Benefits
Comp & perks- An inclusive work environment
- Opportunities for professional development