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We know just how important it is to put people first. It's with that human touch that we've played a part in nearly all of the top 50 treatments on the market. And every day, we're focused on working with industry leaders to bring life-changing healthcare to patients across the globe. Whether you join our Clinical, Consulting, Biotech, Functional Service Provider (FSP), or other teams, we're doing it With Heart ™.

Senior Medical Director, Oncologist (solid tumor)

Job ID R0000007096 Northeast - Remote - United States of America

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

The Senior Medical Director, Oncologist is a recognized medical expert and leader with both specialized therapeutic expertise and broad experience across indications, clients, and drug development. They initiate and maintains medical and consultative relationships with clients, consult on early engagement and pre-award efforts and serve as a medical monitor for contracted projects. The Senior Medical Director, Oncologist may represent Global Medical Services (GMS) on cross-functional initiatives, lead initiatives within GMS, and manages a small team of physicians.

Key Accountabilities

  • Project Execution – Medical Monitoring Delivery and PV Support

  • Client Relationship Building and Engagement

  • Medical Expertise

  • Business Development

  • Department and Team Leadership

Skills / Knowledge and Experience:

  • Experience in clinical with a specialty in oncology (solid tumor), which is expected to be kept up to date

  • A strong background in clinical aspects of drug development, including all aspects of Medical Monitoring and study design/execution

  • Excellent knowledge of the drug development process including drug safety

  • Clinical practice experience

  • Experience working for a CRO highly desirable, or experience working for pharmaceutical and/or biotechnology companies

  • Level of expertise is recognized internally and by others in the industry

  • Client-focused approach to work

  • Excellent interpersonal skills including the ability to interact well with sponsor/client counterparts, internal colleagues and to manage and mentor staff

  • Excellent verbal and written medical and business communication skills

  • Excellent standard of written and spoken English

  • Excellent problem solving, risk assessment and decision-making skills at the department and enterprise level with the ability to analyze business needs and act decisively

  • A flexible attitude with respect to work assignments and new learning

  • Excellent time management skills

  • Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail

  • Willingness to work in a matrix environment and to value the importance of teamwork


  • Board certified in Oncology (solid tumor) with extensive clinical experience. Experience as a Physician in Industry or as a clinical trial investigator is a plus.

  • Medically qualified in an acknowledged medical school with completion of at least a basic training in clinical medicine (residency, internship)

Travel as required by the business


EEO Disclaimer

Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

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