(Sr) Project Manager, Feasibility Site Activation
ICON
ICON seeks a Project Manager or Senior Project Manager for Feasibility and Site Activation to oversee clinical trial site start-up and activation. The role involves managing timelines, coordinating regulatory submissions, tracking progress against KPIs, and serving as the primary contact for internal teams and sponsors across multiple US locations.
Responsibilities
- Develop and manage FSA project plans, timelines, and deliverables for assigned clinical studies
- Coordinate feasibility assessments, site recommendations, and start-up strategies with functional experts
- Oversee essential document collection, regulatory and ethics submissions, and site activation milestones
- Track progress against timelines and KPIs; identify and mitigate risks proactively
- Act as primary FSA contact for internal teams and customers; resolve study issues and represent FSA at audits
Requirements
- Bachelor's degree in life sciences, healthcare, business, or related field
- 3-6 years clinical research experience (Sr. PM); strong site activation or start-up project management background
- Proficiency in project planning, timelines, and cross-functional coordination in fast-paced environments
- Knowledge of regulatory, ethics, and contractual requirements affecting study start-up
- Strong organizational, communication, and stakeholder management skills
- Proficient with Microsoft Office Suite (Word, Excel, PowerPoint, Outlook)
- Ability to work independently and mentor others as needed
Compensation: Competitive base salary and performance related incentives
Vacancy posted a month ago
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