2 дня назад
Senior Project Manager, Feasibility Site Activation
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Project Manager, Feasibility Site Activation (Clinical Research): Planning and coordinating feasibility and site activation activities for clinical studies with an accent on regulatory submissions, site contracts, essential documents, and activation timelines. Focus on driving complex global site start-up projects, managing risks and KPIs, coordinating cross-functional stakeholders, and delivering against sponsor expectations.
Location: Remote or office-based in Boston, Cary, Chicago, Lexington, Los Angeles, Nashville, Portland, Salt Lake City, San Antonio, Whitesboro, Raleigh, Houston, Winston-Salem, Knoxville, Charlotte, Mount Pleasant, Hickory, Rocky Mount, New York, Bristol, Wilmington, Salisbury, Downers Grove, McFarland, Blue Bell, Piedmont, Rochester, Long Beach, or Lawrence, United States.
Company
is a healthcare intelligence and clinical research organization supporting clinical development.
What you will do
- Plan and manage feasibility and site activation activities, project plans, timelines, deliverables, and KPIs for assigned clinical studies.
- Coordinate feasibility assessments, country and site recommendations, and start-up strategies with functional experts.
- Oversee essential document collection, ethics and regulatory submissions, site contracts, and activation milestones.
- Identify risks, implement mitigation plans, resolve study issues, and drive predictable customer delivery.
- Act as the primary FSA contact for internal teams, sponsors, and study stakeholders, including presenting to executive management when needed.
- Represent FSA during audits and inspections, support business development, contribute to process improvements, and mentor colleagues.
Requirements
- Bachelor’s degree in life sciences, healthcare, business, or a related field, or equivalent experience.
- Three to six years of experience in a clinical research environment, with strong feasibility, site activation, or start-up project management experience.
- Experience managing project plans, timelines, competing priorities, and cross-functional coordination with limited supervision.
- Understanding of regulatory, ethics, and contractual requirements affecting clinical study start-up.
- Strong communication, organizational, stakeholder management, mentoring, and prioritization skills.
- Proficiency in Microsoft Office Suite and willingness to travel approximately 10% domestically and/or internationally.
Culture & Benefits
- Inclusive workplace focused on innovation, quality, belonging, and high performance.
- Annual leave entitlements and country-specific flexible benefits.
- Health insurance options for employees and families.
- Retirement planning offerings and life assurance.
- Global Employee Assistance Programme with 24-hour access to specialized support.
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