Oversee site start-up and activation workstreams, ensuring deliverables 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 in collaboration with functional experts
Oversee essential document collection, ethics and regulatory submissions, and site activation milestones
Track progress against timelines and KPIs, proactively identifying risks and implementing mitigation plans
Serve as the primary FSA contact for internal teams and customers for study-level start-up matters
Contribute to process improvement and best practice sharing within the FSA project management team

Bachelor's degree in life sciences, healthcare, business, or a related field, or equivalent experience
Strong experience in clinical research with a focus on feasibility, site activation, or start-up project management
Proven ability to manage project plans, timelines, and cross-functional coordination in a fast-paced environment
Good understanding of regulatory, ethics, and contractual requirements affecting study start-up
Excellent communication, organisational, and stakeholder management skills
Detail-oriented and proactive, with a commitment to quality, predictability, and customer satisfaction
Willingness to travel as required (approximately 10%)

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

Project Manager

Key skills