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Clinical Project Manager- Oncology
- Actalent (Remote, OR)
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Job Title: Local Study Associate Director - Oncology/ Sr. Clinical Project Manager
Job Description
We are seeking a dedicated Local Study Associate Director to join our dynamic oncology team. In this role, you will lead and manage the study team, ensuring strategic oversight of clinical trials at a national level. This position requires a strong leader with the ability to drive study commitments and manage day-to-day trial operations, while coordinating closely with global teams.
Responsibilities
+ Assume overall responsibility for study commitments within the country, ensuring timely delivery of data to the required quality.
+ Lead and optimize the performance of the Local Study Team, ensuring compliance with Procedural Documents, ICH-GCP, and local regulations.
+ Coordinate the site selection process, including identifying potential sites and conducting Site Qualification Visits.
+ Ensure timely submission of application/documents to IRB and Regulatory Authorities.
+ Prepare and maintain accurate study budgets and financial reports.
+ Coordinate local drug activities, from purchase to destruction.
+ Oversee monitoring activities from site activation to study closure, ensuring compliance with Monitoring Plans.
+ Proactively identify and resolve complex study problems and issues.
+ Develop and maintain risk management plans at the country study level.
+ Provide regular updates to the Global Study Leader and Global Study Team.
+ Ensure all study activities comply with local policies and codes of ethics.
Essential Skills
+ 5+ years of hands-on project oversight experience in a similar role.
+ 2+ years as a Project Manager or CRA.
+ 1+ year of Radio conjugate experience.
+ 2+ years of experience in budget build-out and negotiations.
+ Bachelor's degree in a related field.
+ Strong knowledge of international guidelines ICH-GCP and relevant local regulations.
Additional Skills & Qualifications
+ Prior Veeva Clinical Vault experience is preferred.
+ Ability to lead and motivate cross-functional teams.
+ Excellent project management and organizational skills.
+ Strong interpersonal and communication skills.
+ Ability to prioritize and manage multiple tasks effectively.
+ Good negotiation skills.
+ Proficiency in spoken and written English.
+ Willingness to travel nationally and internationally as required.
Work Environment
This role offers a fully remote work environment with some travel required. You will gain high-level project management experience with a leading pharmaceutical company known for its cutting-edge advancements in the industry.
Job Type & Location
This is a Contract position based out of Remote, OR.
Pay and Benefits
The pay range for this position is $65.00 - $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 Jan 23, 2026.
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.
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