Theradex Oncology

Associate Clinical Project Manager

Job Locations US-NJ-Princeton | US
ID
2025-1392
Category
Clinical Project Management
Type
Full Time

Who We Are

Celebrating 40+ Years!

 

Theradex Oncology is a full-service CRO, conducting early- and late-phase oncology trials in the U.S, Europe and Asia. Theradex Oncology was founded in 1982, when we were awarded the Clinical Trials Monitoring Contract for the National Cancer Institute (NCI). Our ongoing association with NCI continues to be a strong basis for our operations. Our focus is cancer. We fully understand the science behind each potential cancer therapy and the challenges that come with moving therapies from mice to man. Theradex Oncology has designed and managed more than 250 early and late-phase oncology trials to date. Our mission is to assure that new discoveries in cancer drug development have the very best opportunity to be of benefit to mankind with a vision to improve treatment and make cancer a livable disease.   

 

What You'll Do

As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will the work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.

 

Location: Remote USA

 

The Associate Clinical Project Manager plays a key role supporting and steering various project specific tasks. Our associate project managers interact with internal and external clients, including sponsors, medical monitors, vendors, quality assurance auditors, study investigators and site representatives. 

 

The primary responsibilities of this position include, but are not limited to, the following:

 
  • Clinical Operations Support: Provide direct support to the Clinical Project Manager on day-to-day operational and tactical study activities.
  • Project Coordination: Assist with tracking project timelines, budgets, and invoice reviews. Serve as a point of contact for external partners.
  • Documentation Management: Manage the Trial Master File (TMF) and ensure accurate filing of clinical operations documentation.
  • Quality Assurance: Support the team's adherence to oversight plans and contribute to internal audits and corrective action plans (CAPA).
  • Study Monitoring: Assist in monitoring study metrics, such as patient enrollment and retention, and support the resolution of identified issues.
  • Risk Mitigation: Help identify potential project risks and assist in developing mitigation strategies.

 

 

 

 

 

 

What You Need

Education and Experience:

  • BSc. required– preferably in a life science field or equivalent, (includes RN degree)
  • MSc. PhD preferred 
  • Healthcare professional with at least 4 years of clinical experience, or Science Graduate with at least 2-3 years’ experience as a Clinical Research Associate / Senior Clinical Research Associate, with a track record in successfully managing clinical trial sites
  • Experience of oncology clinical trials and cancer therapies preferred
  • Prior experience in a CRO/pharmaceutical environment preferred

Skills and Competencies:

  • Effective ability to anticipate problems relating to projects and to develop and implement solutions
  • Fluent knowledge of written and verbal English
  • Knowledgeable of the initiation, conduct, and completion of all phases of oncology clinical trials study endpoints, and clinical databases
  • Knowledgeable in the identification, anticipation and reporting to appropriate management problems relating to study conduct, and highly effective in developing solutions to those problems
  • Knowledge of the drug development process
  • Thorough knowledge of current European and North American regulations and any applicable guidelines
  • Effective ability to set and meet personal short-and long-term goals 
  • Proficient computer skills of MS Office Suite

Additional Requirements:

  • Ability to travel in the US up to 30% when required.
  • Valid Driver’s License an advantage
  • Basic knowledge of one (or more) European language an advantage

 

What We Offer

 

At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for this position ranges from $80,000-$115,000 with bonus potential. The salary offer will be based on a number of factors, including but not limited to the candidate’s qualifications, experience, skills, and competencies for the role.

 

 

 

Theradex is an Equal Opportunity Employer.

 

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