Job Overview
Job description
- Location:
- France
- Work arrangement:
- On-site
Role Summary
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients that need them.
Full-time employment
PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners, while always focusing on patients' safety and well-being.
Responsibilities
- Serve as medical point of contact for internal project team, study sites and study sponsor for medical matters related to the conduct of clinical trials per protocol and per GCP guidelines
- Advise clients, project teams, sites, regulatory agencies and third-party vendors on medical matters
- Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator brochures, annual reports, clinical study reports, patient narratives, and scientific presentations
- Review and analyze of clinical data to ensure the safety of study participants
- Ensure that the reported trial data is accurate, complete, and verifiable, and that the conduct of the trial is in compliance with the currently approved protocol/amendments
- Address safety issues across the trial from sites and the study team
- Provide support for medical data review
- Participate in bid defense meetings and proposal activities
- Assist in Pharmacovigilance activities
- Identify trial risks, and create and implement mitigation strategies with other relevant departments
- Organize and lead clinical development advisory boards and safety monitoring boards
- Ensure Study team compliance with FDA, EMEA, ICH and GCP guidelines
- Medical Doctor degree
- Gastroenterology Fellowship certification is a must
- Prior experience as a practicing MD (minimum of 10 years)
- Prior research and/or clinical trial industry experience is a plus
- Full working proficiency in English
- Proficiency with MS Office applications
- Communication, presentation and analytical skills
- Able to work in teams, problem-solving, and detail-oriented
As part of PSI's Medical Monitoring team, you will join our international group of medical professionals, build a career on the frontline of medical science and use your knowledge and expertise to help bring new medications to patients.
PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights our commitment to delivering high-quality, timely services across a broad spectrum of therapeutic indications.
- At PSI, we foster an environment where a diverse range of colleagues feel welcomed and valued. Our inclusive culture is a cornerstone of our success, enabling us to attract and retain top talent globally.
- We are not just about conducting clinical trials; we are about building a community where every team member has the opportunity to thrive and contribute to groundbreaking advancements in the pharmaceutical industry.
About the Company
Why Join PSI?
At PSI, we believe exceptional people deserve an exceptional workplace.
When you join PSI, you'll benefit from
A stable, privately held CRO that has never undergone a merger or acquisition and has never experienced company-wide layoffs.
A unique leadership-focused CRA role with minimal travel and little to no routine site assignments.
Opportunities to mentor other CRAs and expand your leadership skills.
A collaborative, people-first culture where employees are genuinely supported.
Career development opportunities across a growing global organization.
The chance to contribute to innovative clinical research that improves patients' lives.
We are the company that cares - for our staff, our clients, our partners, and the quality of the work we do.
Founded in 1995, PSI CRO is a privately owned, global Contract Research Organization with more than 3,000 employees dedicated to advancing medical science and bringing new therapies to patients worldwide.
In an industry shaped by mergers, acquisitions, and restructures, PSI stands apart. We have remained privately held, have never undergone a merger or acquisition, and have never experienced company-wide layoffs. Our long-term stability allows us to invest in our people, foster meaningful careers, and build lasting partnerships with our clients.
If you're looking for a collaborative organization where you can continue to grow while making a meaningful impact, PSI is the right place for you.
- Role:
- Medical Monitor (Gastroenterology)
- Job Type:
- Full Time
Company profile
PSI CRO
psi-cro.com- Headquarters
- Kidlington, United Kingdom
- Founded
- 2008