(Sr) Project Manager, Feasibility Site Activation
ICON · Mexico City, Mexico +4 more
The apply link worked recently (not employer-confirmed).
Role summary
This role involves managing feasibility and site activation for clinical studies across Latin America, including planning timelines, coordinating regulatory submissions, and tracking progress against key milestones. The position requires clinical research experience with focus on site start-up, strong project management skills, and understanding of regulatory and ethics requirements. Candidates should have a relevant degree or equivalent background and willingness to travel approximately 10%.
What they're looking for
- Bachelor's degree in life sciences, healthcare, business, or equivalent experience
- Strong clinical research experience with feasibility, site activation, or start-up focus
- Project management skills for plans, timelines, and cross-functional coordination
- Knowledge of regulatory, ethics, and contractual requirements for study start-up
- Excellent communication, organizational, and stakeholder management abilities
- Detail-oriented and proactive with commitment to quality and customer satisfaction
- Willingness to travel approximately 10% as required
What you'll be doing
- Oversee site start-up and activation workstreams to meet quality and timeline expectations
- Develop and manage FSA project plans, timelines, and deliverables for assigned studies
- Coordinate feasibility assessments, country and site recommendations, and start-up strategies
- Track progress against timelines and KPIs, identify risks and implement mitigation plans
- Serve as primary FSA contact for internal teams and customers on study start-up matters
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.