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About the role
Key responsibilities & impact- Main Point of Contact (POC) for assigned protocols
- Responsible for project management of the assigned studies
- Accountable for performance for assigned protocols
- Reviews Monitoring Visits Reports and escalates performance issues
- Performs Quality control visits as required
- Leads local study teams to high performance
- Responsible for creating and executing a local risk management plan
- Ensures compliance with CTMS, eTMF and other key systems
- Collaborates internally with HQ functions
Requirements
What you’ll need- 5-6 years of experience in clinical research
- CRA Experience preferred
- Bachelor's Degree in Science (or comparable)
- Advanced degree (e.g., Master's Degree, MD, PhD) preferred
- Knowledge in Project Management and site management
- Strong organizational skills with demonstrated success required
- Requires ability to make decisions independently
- Strong understanding of local regulatory environment
- Strong scientific and clinical research knowledge is required
- Strong understanding of clinical trial planning, management and metrics is essential
- Communicates effectively and builds collaboration
- Proficiency in written and spoken English and local language
Benefits
Comp & perks- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
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
clinical researchproject managementsite managementclinical trial planningclinical trial managementmetrics analysisrisk managementquality control
Soft Skills
organizational skillsdecision makingcommunicationcollaborationleadership
Certifications
Bachelor's Degree in ScienceMaster's DegreeMDPhD