Clinical Project Manager/Sr

Theradex Oncology; United States; On-site; USD 105,000 - 165,000; Full time

Job summary

Theradex Oncology seeks a Clinical Project Manager/Sr to lead high-impact oncology trials. Ideal candidates possess significant project management experience, particularly in oncology. The role involves direct coordination with sponsors and managing clinical trial sites to ensure adherence to quality standards and timelines, while also offering a comprehensive benefits package.

Benefits

Medical, dental, and vision coverage

Life and disability insurance

401(k) matching

Tuition reimbursement

Flexible work schedules

Qualifications

• 5+ years project management experience in a CRO/pharmaceutical environment.
• Fluent in English, both verbal and written.
• Oncology experience required for Senior level.

Responsibilities

• Oversee global phase I-III clinical trials ensuring timelines and quality standards are met.
• Manage relationships with sponsors, vendors, and investigative sites.
• Identify risks and implement solutions for successful trial completion.

Skills

Leadership

Critical Thinking

Analytical Skills

Communication Skills

Education

BS in Life Science or equivalent

MS or PhD preferred

Tools

Excel

MS Office

Job description

Join to apply for the Clinical Project Manager/Sr role at Theradex Oncology

Join to apply for the Clinical Project Manager/Sr role at Theradex Oncology

About Us: Theradex Oncology is a leading global oncology CRO, in business for over 40 years. We support many of the most prominent pharmaceutical and biotech companies in the industry with promising new molecules that address a wide range of oncology indications. We provide a supportive environment through our expertise, innovative systems and processes and we give you the tools to be successful as we grow our Clinical Operations Team.

We are looking for a Clinical Project Manager or Sr Project Manager (dependent upon experience) to oversee high-impact clinical studies on behalf of our sponsors. Senior Project Manager candidates must have oncology experience.

About the Role: Theradex Project Managers oversee global phase I – III clinical trials from feasibility and startup through closeout to ensure processes, timelines, contracts, ICH/GCP adherence and quality standards are met. As a primary point of contact, our project managers are hands-on and interface directly with our sponsors, vendors, cross-functional team members and investigative sites. They identify and evaluate risks, interpret data on complex issues and implement solutions to ensure successful completion of oncology trials.

Qualifications:

• Education: BS. required– preferably in a life science field or equivalent (includes RN degree) MS. or PhD. preferred

Requirements:

• You must have proven experience with oncology clinical trials and/or cancer therapies (for senior level role)
• Must be fluent in English (verbal and written)
• 5+ years of prior project management experience with demonstrated leadership skills in a CRO/pharmaceutical environment, with a track record in successfully managing clinical trial sites for Sr level project manager.
• 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 for project manager level.
• High level of proficiency with Excel and MS Office; ability to master various electronic platforms for data entry and clinical trial management
• Experience with CAR-T cell therapy/trials highly preferred
• Ability to travel occasionally up to 30% domestically when required
• Valid Driver’s License

Skills and Competencies:

• 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

Relocation assistance or company provided sponsorship is not offered for this position.

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 $105,000-$165,000 with bonus potential. We will assess the specific title and level of entry during the interview and assessment process since the actual 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.

For additional details on responsibilities and requirements needed, please click on the link to view and/or apply.

Theradex is an Equal Opportunity Employer.

#CRO #oncology #clinicaltrials #CRA #hiringnow #careersthatmatter

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Project Management

• Industries

  Biotechnology Research and Pharmaceutical Manufacturing

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Inferred from the description for this job

Medical insurance

Vision insurance

401(k)

Tuition assistance

Disability insurance

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