Regional Clinical Trial Manager

As a Regional Clinical Trial Manager, you will oversee the day-to-day operations of clinical trials within your designated region, ensuring compliance with protocols, ICH GCP, and regulatory requirements. You will work closely with CRO partners, study vendors, and cross-functional team members to ensure successful trial execution, leading activities that promote quality, consistency, and cross-functional alignment.

• Manage clinical trials in LATAM (Brazil and Argentina), overseeing CRO vendors and other study vendors.
• Ensure timely shipments of vendor supplies to LATAM sites, including Central Lab kits.
• Manage study budgets, timelines, and metrics, ensuring adherence.
• Oversee Study Start-Up activities, site selection, activation timelines, and contract negotiations.
• Serve as the primary escalation point for regional and site-related issues.
• Participate in weekly meetings with CRO partners and study vendors, ensuring cross-functional alignment.
• Review study-related clinical plans and documents.
• Perform quality and monitoring oversight activities, ensuring audit‑ready condition of clinical trial documentation.
• Conduct Monitoring Oversight visits to assess compliance, as required.
• Oversee participant recruitment and retention strategies.
• Coordinate regulatory and ethics committee submission activities, ensuring compliance with local regulatory requirements.
• Assist with Investigator and Site Initiation visits.

• Bachelor's degree in Life Sciences, Nursing, or equivalent.
• Minimum 5 years of experience in Clinical Operations.
• Minimum 3 years of experience in clinical study management.
• Hands‑on experience managing studies in LATAM.
• Spanish and/or Portuguese speaking is preferred.

• Ph.D. in a related life science discipline is preferred.
• Operational experience managing at least two studies as a regional CTM for LATAM.
• Knowledge of regulatory requirements in Brazil.
• Ability to travel approximately 20% of the time to LATAM.

This is a remote role, with a preference for candidates located on the east coast. The position requires the ability to travel approximately 20% of the time, particularly to Brazil and Argentina.

This is a Contract position based out of Boston, MA.

The pay range for this position is $70.00 - $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)

This is a fully remote position.

This position is anticipated to close on Feb 27, 2026.

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 actalentaccom for other accommodation options.