• Sr. Clinical Trial Manager

    Actalent (New York, NY)


    Sr. Global Clinical Trial Manager

     

    Small Sponsor company

     

    + 10-15 years of Clinical Research experience required

    + 5+ years of recent, oncology CTM experience

    + Strong CRO/Vendor Oversight Experience

    + BS/BA degree Minimum

    Description

    Job Description (Day to Day Responsibilities): The Clinical Trials Manager (CTM), Clinical Operations, coordinates the activities associated with the evaluation, initiation, and management of clinical trials. This position is responsible for overseeing the execution of clinical trials, collaborating with cross-functional teams, performing oversight activities of Contract Research Organizations (CROs), and providing operational support to the Study Delivery Lead (SDL).

    Specific Tasks:

    • Manage clinical trial activities for assigned programs ensuring compliance with ICH GCP, US FDA, EMEA and applicable regulations; may lead the development of all study-related plans necessary for trial conduct.

    • Manages clinical trials, including those conducted through Contract Research Organizations (CROs)

    • May participate in developing and recommending operational strategies for clinical trials in collaboration with cross-functional teams

    • Responsible for at least one geographical region and manages/oversees one to three external vendors within a specific scope (e.g., Lab)

    • Engages with CROs, vendors and sites for ongoing trial execution, including relationship management and quality / performance oversight

    • Provides CRO oversight on activities related to site start-up and maintenance, including reviewing trip reports, protocol deviations, data review, etc

     

    Full time; Long term contract role paid hourly but fully embedded and renewable. Initial client contract through End of 2026 then to be renewed

     

    Additional Skills & Qualifications

    Qualifications (What are the Required Capabilities):

    • 10+ years Clinical Research Experience

    • 5+ yrs of recent Global Oncology Clin Ops Exp -- doing Vendor Oversight Trial Management

    • Willingness to travel up to 20% in the US

    • BS/BA/BSN in Biological Sciences or related field

    Culture Fit (Soft Skills)

    • Strong team player; ability to work within a national/remote team.

    • Flexibility and successful history in managing workload that spans across multiple time zones

    • Eagerness to learn and grow within the role

    • Ability to pivot quickly to manage competing priorities in a fast paced environment

    Experience Level

    Expert Level

    Pay and Benefits

    The pay range for this position is $78.00 - $82.00/hr.

     

    Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

     

    • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)

     

    Workplace Type

     

    This is a fully remote position.

     

    Application Deadline

     

    This position is anticipated to close on Oct 3, 2025.

    About Actalent

    Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

     

    The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

     

    If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email [email protected] (%[email protected]) for other accommodation options.