Parexel Medical Director, Endocrinology Recruitment 2026: Apply Online for Various Vacancies
Medical Director, Endocrinology
Job Overview
Parexel’s endocrinology team brings deep expertise across the full clinical spectrum—from rare metabolic disorders to programs in obesity and diabetes. We are excited to be expanding our team in Canada, offering a unique opportunity to contribute to cutting-edge research that is shaping the future of patient care. We currently have an exciting opportunity available for an Associate/Medical Director/Senior Medical Director, Endocrinology to join our exceptionally talented and patient-focused General Medicine team.
As a Medical Director, you will provide medical monitoring for assigned projects, function as the medical representative on the project team, provide medical consultation as required or requested to client/sponsor or to other Parexel service groups, and assume the role of Senior Technical Lead in selected circumstances. This role offers a dynamic environment where clinical expertise meets global drug development strategy.
Key aspects of this remote position include:
- Providing comprehensive medical oversight and monitoring for global clinical trials in endocrinology and metabolic diseases.
- Collaborating with cross-functional teams to ensure patient safety and data integrity throughout the lifecycle of clinical projects.
- Reviewing safety data, including laboratory values and adverse events, to identify and mitigate potential risks.
- Interfacing directly with biotech and pharmaceutical sponsors to provide strategic medical guidance and clinical trial design insights.
- Contributing to the development of clinical protocols, investigator brochures, and regulatory submission documents.
Key Job Details
| Company Name | Parexel International |
| Job Role | Medical Director, Endocrinology |
| Experience | Extensive clinical experience treating adult patients with Obesity, MASH/NASH, and Diabetes is highly preferred. Past experience as a Physician in Industry or as a Clinical Trial PI/Sub-I is highly preferred. |
| Salary Range | Not Disclosed |
| Job Type | Full-time |
| Work Mode | Remote |
| Openings | Various |
| Job Location | Canada (British Columbia – Remote) |
Key Responsibilities
- Review all individual adverse experience reports for accuracy and clinical importance, and characterize their relationship to the study drug, severity, and seriousness.
- Provide reports to FDA or other regulatory agencies and the sponsor on a periodic and regular basis, summarizing adverse experiences as required by FDA or the sponsor, depending on the contract.
- Review data listings of safety data, including adverse experiences, laboratory data, and vital signs data, to establish the presence or absence of abnormal trends, and if noted, follow up as appropriate with the project team, sponsor, investigator, and FDA.
- Review documents written by various Parexel divisions for safety issues.
- Review coding of adverse events and concomitant medications for accuracy and consistency.
- Provide support for the preparation of clinical protocols, integrated clinical and statistical summary reports, journal articles, and other documents for clients/sponsors or in conjunction with clients/sponsors and in conjunction with other Parexel divisions.
- Attend and present material, as requested, at meetings within Parexel as well as extra-company external meetings and conferences.
Requirements & Qualifications
- Must be an MD Endocrinologist with FRCPC certification (or equivalent international credential).
- Extensive clinical experience treating adult patients with Obesity, MASH/NASH, and Diabetes is highly preferred.
- Past experience as a Physician in Industry or as a Clinical Trial Primary Investigator or Sub-Investigator is highly preferred; however, consideration will be given to exceptional candidates with an interest in transitioning to Industry.
- Ability to travel up to 20% domestically and/or internationally as needed.
Required Skills
- Excellent interpersonal skills including the ability to interact well with sponsor/client counterparts.
- Excellent time management skills.
- Excellent verbal and written medical communication skills.
- Excellent standard of written and spoken English.
- A flexible attitude with respect to work assignments and new learning.
- The ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail.
- A willingness to work in a matrix environment and to value the importance of teamwork.
About Parexel International
Parexel is one of the world’s largest clinical research organizations (CRO), providing the full range of Phase I to IV clinical development services to help life-saving treatments reach patients faster. With a compassionate and results-driven work culture, Parexel prioritizes patient care, clinical excellence, and employee growth across its global operations.
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