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Posted: 9/15/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive experience in clinical research, site management, and oversight, with a strong understanding of ICH-GCP and regulatory requirements. Proven ability to build relationships with stakeholders and manage site performance to drive successful study outcomes.
Highest-signal resume keywords
Clinical Research ExperienceSite ManagementICH-GCP ComplianceStakeholder ManagementRisk Management
About the role
Key responsibilities & impact- Oversee scientific operations workstreams, ensuring deliverables meet quality and timeline expectations
- Build and maintain relationships with investigators, site staff, and key stakeholders
- Act as the primary liaison between sites, CRO partners, and internal study teams
- Evaluate site capabilities and performance for site identification, feasibility, and selection
- Oversee site-level study start-up, activation, conduct, and close-out activities
- Support site contracting and activation with internal teams and external vendors
- Monitor site performance, recruitment, enrollment, quality, and compliance metrics
- Identify risks and implement mitigation plans
- Drive site engagement strategies and develop action plans to improve performance, recruitment, and retention
- Oversee CRO-delivered site management activities and ensure compliance with ICH-GCP, regulatory requirements, and company procedures
- Collaborate with Clinical Operations, Study Management, Medical Affairs, Regulatory Affairs, and other stakeholders
- Use site and study performance data to identify trends, support decisions, and contribute to process improvement
- Manage competing priorities and develop the team
Requirements
What you’ll need- Degree in Life Sciences, Pharmacy, Nursing, Medicine, or a related scientific discipline
- 8+ years of clinical research experience within a CRO, pharmaceutical, biotechnology, or healthcare environment, including site management, site oversight, monitoring, clinical operations, or study management
- Strong understanding of clinical trial conduct, global drug development, ICH-GCP, and applicable regulatory requirements
- Experience working with and overseeing CROs and external vendors
- Proven ability to build strong relationships with investigators, site personnel, and cross-functional stakeholders
- Strong analytical, risk management, problem-solving, and decision-making skills
- Excellent communication, stakeholder management, and organizational abilities
- Experience supporting study start-up, site activation, recruitment, enrollment, and site performance management
- Experience with CTMS, eTMF, and other clinical trial systems is preferred
- Ability to travel domestically and internationally up to 50%
- Legal right to work in the country where the role is based
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
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 ConductSite ActivationRecruitment ManagementEnrollment ManagementSite Performance MonitoringData AnalysisProblem-SolvingDecision-Making
Soft Skills
CommunicationOrganizational AbilitiesRelationship Building
Tools & Technologies
CTMSETMF
Industry Keywords
CROPharmaceuticalBiotechnologyHealthcareGlobal Drug Development