Senior Project Manager, Feasibility Site Activation
Posted 10 hours ago
Posted 10 hours ago
This is a fully remote position, open to applicants in California, +12 more states.
• Plan and oversee the Feasibility and Site Activation activities for designated clinical studies.
• Manage site start-up and activation processes, ensuring that quality and timeline goals are achieved.
• Create and maintain FSA project plans, timelines, and deliverables.
• Coordinate feasibility evaluations, site and country recommendations, and start-up strategies.
• Supervise the collection of essential documents, ethics and regulatory submissions, and site activation milestones.
• Monitor progress against timelines and KPIs, identify potential risks, and apply mitigation strategies.
• Act as the primary FSA liaison for internal teams and clients concerning study-level start-up issues.
• Accelerate the activation of global investigative sites within set timelines, budgets, and quality standards.
• Organize, implement, and finalize site activation tasks for large-scale global or complex projects.
• Engage with internal teams, sponsor teams, and stakeholders; present findings to Executive Management when necessary.
• Review study and partnership budgets for proposals and sales opportunities.
• Propel assigned studies to achieve KPIs and deliver outstanding customer and site results.
• Serve as the customer contact point, addressing study-related issues and supporting customer satisfaction.
• Represent FSA during audits and inspections.
• Engage in business development initiatives.
• Mentor colleagues and contribute to process enhancements and the sharing of best practices.
• Conduct activities in accordance with corporate and departmental policies, SOPs, and operational guidelines.
• Bachelor’s degree in life sciences, healthcare, business, or a related field, or equivalent experience.
• Bachelor's Degree.
• 3-6 years of experience in a Clinical Research setting.
• Extensive experience in clinical research with an emphasis on feasibility, site activation, or start-up project management.
• Demonstrated ability to manage project plans, timelines, and cross-functional coordination in a fast-paced setting.
• Strong understanding of regulatory, ethics, and contractual obligations impacting study start-up.
• Excellent communication, organizational, and stakeholder management skills.
• Detail-oriented and proactive, with a strong commitment to quality, predictability, and customer satisfaction.
• Proven organizational skills with the ability to prioritize tasks independently with minimal supervision.
• Proficient in Microsoft Office Suite applications, including Word, Excel, PowerPoint, and Outlook.
• Ability to complete tasks efficiently and on time without assistance.
• Capability to mentor and train others as necessary.
• Legal authorization to work in the country where the position is based.
• Willingness to travel as needed, approximately 10% of the time.
• Competitive base salary along with performance-related incentives.
• Health and wellness programs, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life insurance and disability coverage.
• Employee assistance programs and wellness resources.
• Learning and development opportunities through structured training and career pathways.
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