Clinical Trial Manager

Actalent; Raleigh (NC); Remote; USD 60,000 - 80,000; Full time

Job summary

A leading company is seeking a Clinical Trial Manager to oversee US sites for oncology medical device trials. You will collaborate with cross-functional teams, manage vendor operations, and ensure compliance with regulatory standards. This is a fully remote position, offering a competitive hourly rate and extensive benefits, including medical, dental, and vision coverage.

Benefits

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account (HSA)

Employee Assistance Program

Time Off/Leave

Qualifications

• 3+ years of Clinical Trial Management (CTM) experience required.
• Proven vendor oversight experience.
• Experience in managing medical device trials.
• Knowledge of medical device regulations is advantageous.

Responsibilities

• Serve as the primary point of contact for US sites.
• Collaborate with the Lead CTM and ensure cohesive trial management.
• Oversee vendor operations and maintain continuous site interaction.

Skills

Clinical Trial Management

Vendor oversight

Oncology experience

Communication skills

Job description

Join to apply for the Clinical Trial Manager role at Actalent

Join to apply for the Clinical Trial Manager role at Actalent

Senior Clinical Trial Manager Medical Device/Oncology

Responsibilities

• Serve as the primary point of contact (POC) for US sites, supporting study follow-up and data clean-up.
• Collaborate with the Lead CTM and EU CTM to ensure cohesive trial management.
• Oversee vendor operations, including central labs, imaging, and shipments.
• Maintain continuous site interaction, effective site management, and budget adherence.
• Work closely with Key Opinion Leaders (KOLs) and manage the complexities of combination devices within the trial.
  
  

Essential Skills

• 3+ years of Clinical Trial Management (CTM) experience.
• Proven vendor oversight experience.
• Experience in managing medical device trials and pharmaceutical drug trials.
• Recent experience in oncology medical device trials with a focus on liver solid tumors is highly desirable.
  
  

Additional Skills & Qualifications

• Device and Pharma experience, especially in oncology.
• Experience with Sponsor and Clinical Research Organizations (CROs).
• Strong communication skills and ability to work collaboratively in a team.
• Knowledge of medical device regulations is advantageous.
  
  

Pay and Benefits

The pay range for this position is $66.00 - $70.00/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 Jun 27, 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 [e-mail] for other accommodation options.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Contract

Job function

• Job function

  Research, Analyst, and Information Technology

• Industries

  Business Consulting and Services

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