Sr. Clinical Project Manager - Oncology - new job in Remote, US

Sr. Clinical Project Manager - Oncology
  • Competitive
  • Permanent
  • Remote TX, US Remote TRAVIS US
Job Ref: JO000136496
Sector: Clinical
Sub-sector: Clinical
Date Added: 23 May 2023

Job Title: Sr Clinical Project Manager (Oncology)
Job Type: Permanent Full-Time
Location: 100 % Remote

** Candidates must have experience in Oncology Clinical Research trials.

We are searching for a permanent full-time Senior Clinical Project Manager (Oncology Studies) to join a global Contract Research Organization (CRO) providing a comprehensive range of services in clinical development.


Responsibilities include, but are not limited to:

  • Oversee all aspects of clinical research projects to assure applicable regulations, standard operating procedures, and sponsor requirements are met.
  • Perform contract and financial management activities for assigned trials and serves as central point of contact with sponsor for project updates.
  • Participate in business development activities, including proposal development and pricing and bid defense meetings, as required.
  • Maintains and manages overall study budget and identifies and informs team of budget constraints.
  • Identifies study risk and develops mitigation strategies and contingency plans.
  • Provides leadership and coordination to matrix project team members that may include clinical research associates, clinical data analysts, vendors, contractors, and consultants as required by the project.


  • Bachelor’s degree in a Pharmacy, Medicine, Life Sciences, Nursing, or a related field.
  • Minimum of 5 years of project management experience in Oncology Clinical Trials within a CRO, pharmaceutical, biotechnology or medical device company.
  • Minimum of 3 years of experience directly managing professional-level individuals; leading multi-service project teams through clinical trials, in a clinical research global environment.
  • Experience with clinical, regulatory, and data aspects of trials, including but not limited to field monitoring, data management, biostatistics, and medical writing.
  • Experience abiding by FDA Guidelines, ICH, GCP, NDA, IND, and other applicable regulations

** Only candidates selected to be moved forward in the recruitment process will be contacted by SRG's Recruitment Team to schedule a conversation.

SRG is an Equal Opportunity Employer. All qualified applicants will receive consideration without regard to race, color, religion, gender, national origin, age, disability, veteran status, or any other factor determined to be unlawful under applicable law.

23/06/2023 12:00:00
USD 0.00 0.00 Hour
Contact Consultant:
Kyle Kessler

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