Clinical Trial Manager

Actalent; Durham (NC); Remote; Full time

Job summary

Actalent is seeking a Clinical Trial Manager to oversee and manage clinical trials, focusing on oncology and device integration. Responsibilities include liaising with clinical sites, ensuring compliance, and managing vendor operations. This fully remote role offers a competitive salary and comprehensive benefits, making it an excellent opportunity for experienced professionals in the field.

Benefits

Medical, dental & vision insurance

401(k) Retirement Plan

Life Insurance

Short and long-term disability

Health Spending Account

Transportation benefits

Time Off/Leave

Qualifications

• 3+ years of Clinical Trial Management experience required.
• Experience in managing medical device and pharmaceutical trials is crucial.
• Strong communication skills and collaborative abilities are essential.

Responsibilities

• Serve as primary point of contact for US study sites.
• Collaborate with team to ensure cohesive trial management.
• Oversee vendor operations and maintain site interactions.

Skills

Clinical Trial Management

Vendor Oversight

Communication

Team Collaboration

Job description

Join to apply for the Clinical Trial Manager role at Actalent

1 day ago Be among the first 25 applicants

Join to apply for the Clinical Trial Manager role at Actalent

Get AI-powered advice on this job and more exclusive features.

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

Referrals increase your chances of interviewing at Actalent by 2x

Sign in to set job alerts for “Clinical Trial Manager” roles.

Associate Director, Decentralized Clinical Trials

Senior Clinical Quality Assurance Manager

Raleigh, NC $80,000.00-$100,000.00 8 hours ago

Senior Clinical Research Associate - Obesity - West Coast - Remote

Senior Clinical Research Associate - Obesity - East Coast - Remote

Senior Clinical Research Associate - Rare Disease - East Coast - Remote

Sr Clinical Research Associate - Sponsor Dedicated - Oncology (Home-Based in Western US)

Morrisville, NC $80,600.00-$145,000.00 6 days ago

Senior Clinical Research Associate - CNS/Ophthalmology - Upper Midwest - Remote

We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.