Senior Clinical Project Manager

1w1 week ago

Recursion

New York City, US · Full-time · $168,000 – $204,800

About this role

Recursion is at the forefront of reimagining drug discovery through automated cell biology, high-dimensional data sets, and sophisticated analytics. We seek a Senior Clinical Project Manager in Clinical Operations to manage one or more clinical trials from study start-up to closure. This role receives support or direction from a Director of Clinical Operations.

Lead all aspects of clinical trial execution from IND through proof-of-concept and pivotal studies. Plan and oversee global clinical trials, including study budgets, financial reporting, and forecasting with Clinical Outsourcing. Develop strong relationships with cross-functional teams, CROs, investigators, and stakeholders.

Report to a Director of Clinical Operations as an essential member of the Clinical Operations team within Development. This dedicated team ensures operational excellence across clinical programs. Join an empowered, execution-minded group translating innovative science to patients.

Manage clinical trial operations, lead study teams including CROs and vendors, and report on start-up, conduct, and close-out activities. Ensure compliance with study protocols, SOPs, GCP, ICH, and local regulations. Your work will change lives, including your own.

Requirements

Bachelor’s degree in a scientific or healthcare-related field
7+ years of experience in a clinical operations role in the biopharmaceutical industry, with at least 3+ years in a clinical project management role within a biotech organization
Early phase (Phase 1, 2) oncology experience at a biotech/Sponsor required
Demonstrated experience organizing and leading clinical study teams
Demonstrated track-record of efficient and effective clinical trial planning and execution, including risk management and mitigation strategies
Experience in vendor and CRO selection, management, and oversight
Experience managing and tracking study budgets and financials with participation in invoice and contract review and approvals
Excellent working knowledge of FDA, ICH, GCP regulations and guidelines

Responsibilities

Lead all aspects of clinical trial execution for one or more programs from IND through proof-of-concept and pivotal studies
Plan and oversee implementation, coordination, and execution of global clinical trials including oversight of study budgets, financial reporting, and forecasting
Develop and maintain strong relationships with cross-functional study teams, CROs, clinical investigators, and clinical trial stakeholders
Manage clinical trial operations and lead study teams, including CROs and vendors, and reporting of start-up, conduct, and close-out activities
Ensure compliance with study protocol and applicable Standard Operating Procedures (SOP), Good Clinical Practices (GCP), ICH and local regulations