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PA

Parexel

via Workday

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Medical Director, Gastroenterology

Anywhere
Full-time
Posted 1/8/2026
Direct Apply
Key Skills:
Medical oversight
Clinical trial design
Pharmacovigilance

Compensation

Salary Range

$200K - 300K a year

Responsibilities

Lead medical excellence in gastroenterology clinical trials, ensuring scientific integrity and patient safety, and contribute to drug development strategies.

Requirements

MD or DO with clinical practice experience, understanding of clinical medicine, and preferably experience in industry or clinical trials, with excellent communication and collaboration skills.

Full Description

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. Medical Director - Gastroenterology Specialty Location: Remote - United States / Travel: 15-20% About This Opportunity Parexel is seeking an exceptional Medical Director with specialized expertise in Gastroenterology to join our Medical Sciences team. This is an outstanding opportunity for a physician looking to leverage their clinical expertise in the dynamic field of clinical drug development. As a medical expert and strategic partner, you'll play a pivotal role in advancing therapeutic innovations while building meaningful relationships with pharmaceutical sponsors and contributing to life-changing treatments for patients worldwide. What You'll Do Lead Medical Excellence in Clinical Trials Serve as Medical Monitor for gastroenterology studies, ensuring scientific integrity and patient safety Provide expert medical oversight throughout the clinical trial lifecycle—from protocol development through study completion Review and approve critical study documents including protocols, Medical Monitoring Plans, safety reports, and Informed Consent Forms Conduct real-time medical data review, evaluate protocol deviations, and ensure medical accuracy across all study deliverables Drive Client Success & Relationships Build and maintain consultative relationships with pharmaceutical sponsors Deliver medical expertise during client meetings, bid pursuits, and proposal development Provide therapeutic area training to study teams and site personnel Respond to complex medical and protocol-related questions from sites and study teams Shape Drug Development Strategy Participate in early engagement activities and feasibility assessments Contribute medical insights to protocol design and drug development programs Support pharmacovigilance activities including medical review of serious adverse events Provide risk assessments for clinical trial sponsorship Collaborate & Innovate Work in a dynamic matrix environment with cross-functional project teams Support business development initiatives with your gastroenterology expertise Contribute to thought leadership through white papers, publications, and training modules Participate in emergency medical contact rotations as needed What You Bring Required Qualifications MD, DO, or equivalent medical degree with clinical practice experience Active or prior medical licensure, or equivalent comparable clinical training Strong understanding of clinical medicine and patient care principles Preferred Experience Past experience as a Physician in Industry or as a Clinical Trial Investigator Experience with medical monitoring and clinical trial design/execution Knowledge of drug safety and pharmacovigilance processes Essential Skills Exceptional communication skills – both written and verbal medical communication Client-focused mindset with excellent interpersonal abilities Superior time management and ability to prioritize multiple projects Attention to detail with strong analytical and critical thinking capabilities Collaborative approach and comfort working in matrix teams Flexibility and adaptability to evolving project needs Proficiency in written and spoken English Why Parexel? At Parexel, you'll join a global leader in clinical research with a mission to improve global health. We offer: Meaningful Impact: Contribute to therapies that change patients' lives Professional Growth: Expand your expertise across therapeutic areas and drug development phases Collaborative Culture: Work with world-class medical and scientific professionals Flexibility: Remote work arrangement with work-life balance Innovation: Access to cutting-edge clinical research and medical technologies Ready to Make a Difference? If you're a gastroenterology specialist passionate about advancing medical science and improving patient outcomes through clinical research, we want to hear from you. Apply today and help shape the future of drug development. 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. Parexel is a leading global clinical research organization (CRO) providing insights-driven Clinical and Consulting solutions to the world’s life sciences industry. Leveraging deep local knowledge and a global breadth of clinical, regulatory and therapeutic expertise, our professionals worldwide work in partnership with biopharmaceutical leaders, emerging innovators and sites to design and deliver clinical trials with patients in mind — broadening access and making clinical research a care option for anyone, anywhere. Our proven track record spans 40+ years and drives us forward, advancing clinical research in healthcare’s most complex areas while harnessing innovation to drive efficiencies across every phase of the clinical development process. Our insights-driven approach, proven delivery and trusted execution are accelerating the delivery of life-changing treatments to patients — With Heart.™

This job posting was last updated on 1/9/2026

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