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%.
Responsibilities
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
Requirements
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