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Medical Director, Medical Affairs, Psychiatry - U.S Remote

Remote / Online - Candidates ideally in
Essex County, Canada
Listing for: Worldwide Clinical Trials
Full Time, Remote/Work from Home position
Listed on 2025-12-02
Job specializations:
  • Healthcare
    Clinical Research, Medical Science
Salary/Wage Range or Industry Benchmark: 150000 - 200000 CAD Yearly CAD 150000.00 200000.00 YEAR
Job Description & How to Apply Below
Position: Medical Director, Medical Affairs, Psychiatry - U.S. - Remote

Medical Director, Medical Affairs, Psychiatry - U.S.

- Remote

Join to apply for the Medical Director, Medical Affairs, Psychiatry - U.S.

- Remote
role at Worldwide Clinical Trials
.

5 days ago. Be among the first 25 applicants.

Who we are

We are a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity, and we are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us!

What a Medical Director, Psychiatry does at Worldwide Clinical Trials

Medical Affairs plays a pivotal role throughout the entire life cycle of a clinical investigation, exerting its influence from the initial stages of Business Development to the final Regulatory Submissions. Within this multifaceted domain, the dedicated members of the Medical Affairs team provide essential support to the broader project team, contributing to the cultivation of the scientific and medical principles that define Worldwide's philosophy.

Collaboration is a cornerstone of Medical Affairs, as you work closely with other functional groups within the Worldwide organization. As a member of our team, you will have the opportunity to engage in the entire spectrum of clinical investigation activities, from initial database construction to the final delivery of project datasets. Within Medical Affairs, you will discover a diverse range of roles, including direct interactions with pharmaceutical companies, protocol preparation, feasibility assessments, training of site staff, medical monitoring, pharmacovigilance, and medical writing.

These roles present ample opportunities for you to excel and contribute your unique talents to our mission to impact millions of patients' lives around the globe!

What You Will Do
  • Collaborate with the other members of the Medical & Safety project teams to process Serious Adverse Events (SAEs)
    Contribute medical input into the design of clinical development programs, study protocols, research papers, client-focused white papers, etc.
  • As directed support Business Development through participation in proposal generation, feasibility assessments, review of proposals/contracts for medical services, and attendance at meetings with sponsors as directed by department senior management.
  • Review and/or assist in the preparation of final study reports (CSRs), or other study documentation (Protocols, ISS/ISEs, etc.) as directed by senior management.
  • Maintain a high level of competence with assigned projects, including knowledge of project and therapeutic advances as well as marketplace developments by participating in internal meetings (company-wide project tracking, medical management meeting, etc.), review of relevant therapeutic/clinical literature, and attendance in conferences and meetings.
  • Assist in the mentoring of other medical staff as directed by Senior Management and by consistently displaying exemplary work ethics, compassion, and integrity, supporting Senior Management’s leadership of both the department and the company.
What You Will Bring To

The Role
  • Excellent computer skills (Word, Excel, Access)
  • Excellent spoken and written English skills
  • Excellent organizational and time management skills
  • Excellent presentation skills
Your Experience
  • Medical Degree from an accredited institution of Medical Education with a Psychiatry focus
  • At least 2 years of medical monitoring in a CROValid passport and ability to travel as required
Exact compensation may vary based on skills, experience, and location

$ - $

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit or connect with us on Linked In.

Senior level

Mid-Senior level

Employment type

Full-time

Job function

Health Care Provider

Industry

Research Services

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