[Hiring] Clinical Project Manager @Theradex Oncology

Role Description

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 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.

Clinical Project Manager or Sr Clinical Project Manager based on experience.

Location: USA Remote

Theradex Project Managers oversee global phase I – III oncology clinical trials from feasibility and startup through closeout to ensure processes, timelines, contracts, ICH/GCP adherence and quality standards are met.

As a key point of contact, you'll interface directly with sponsors, vendors, cross-functional team members, and investigative sites. You'll identify and evaluate risks, interpret data on complex issues, and implement solutions to ensure successful completion of oncology trials.

Qualifications

• BS required – preferably in a life science field or equivalent (includes RN degree)
• MS or PhD preferred
• Healthcare professional with at least 4 years of clinical experience, or Science Graduate with at least 4 years experience in clinical research, with a track record in successfully managing clinical trial sites
• Prior project management experience required
• High level of proficiency with Excel and MS Office; ability to master various electronic platforms for data entry and clinical trial management
• Experience with oncology clinical trials and/or cancer therapies is highly preferred (required for senior level project managers)
• Prior involvement with CAR-T or other gene/cell therapies is highly preferred
• Prior experience in a CRO/pharmaceutical environment preferred (required for senior level project managers)
• Must be fluent in English (verbal and written)

Requirements

• Well-developed critical thinking and analytical skills, with the ability to anticipate problems relating to projects and to develop and implement solutions
• Able to seek out multiple and diverse perspectives; open to continuously refining your approach based on feedback and new information
• Knowledgeable of the initiation, conduct, and completion of clinical trials, study endpoints, and clinical databases
• Well-developed and effective written and verbal communication skills, including report writing, preparing, and delivering presentations, and various correspondence and meeting platforms
• Effective knowledge of the drug development process

Benefits

• 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
• Annual base salary for this position ranges from $105,000-$165,000 with bonus potential