Remote Contract Clinical Trial Manager - Oncology

Actalent; Waltham (MA); Remote; USD 110,000 - 124,000; Full time

Benefits offered by this job

Medical, dental & vision

401(k) Retirement Plan

Life Insurance

Disability coverage

Health Spending Account (HSA)

Transportation benefits

Paid time off (PTO)

Job summary

Actalent is seeking a Clinical Trial Manager to oversee global trial operations from a remote basis. You will manage project timelines, CRA monitoring, and vendor relationships, ensuring compliance with GCP, FDA, and ICH guidelines.

Applicants should have 3–5+ years in trial management, 3+ years oncology experience, budgeting and contracts expertise, and strong cross‑functional communication. Some travel (5–10%) may be required; EST/remote work preferred.

Qualifications

• 3-5+ years of Clinical Trial Management experience.
• 3+ years of oncology experience.
• Experience with study budgets, contracts, and invoicing.
• Sponsor experience.
• Working knowledge of GCPs and FDA and ICH regulations.
• Ability to lead effective meetings and cross-functional communication.

Responsibilities

• Supervise all aspects of Clinical Trial Operations, including project management and study center activities.
• Oversee CRA monitoring activities and vendor management.
• Ensure effective cross-functional communication of important study decisions and milestones.
• Lead effective meetings and demonstrate good judgment.
• Ensure trials are conducted in accordance with GCPs, FDA, and ICH regulations and guidelines.
• Manage external service providers and international clinical trials in regions including EU, CA, and Australia.

Skills

Clinical Trial Management

Oncology experience

Budgeting & invoicing

Sponsor experience

GCP FDA ICH knowledge

Cross-functional communication

Education

Bachelor's Degree in life sciences

Job description

Actalent is seeking a Clinical Trial Manager to oversee global trial operations from a remote basis. You will manage project timelines, CRA monitoring, and vendor relationships, ensuring compliance with GCP, FDA, and ICH guidelines.

Applicants should have 3–5+ years in trial management, 3+ years oncology experience, budgeting and contracts expertise, and strong cross‑functional communication. Some travel (5–10%) may be required; EST/remote work preferred.