Clinical Trial Physician
Clinical Trial Physician
Posted on :
01-04-2025
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1 Vacancy
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Hourly Salary
CHF CHF 65 - 77
Vacancy
1 Vacancy
Posted on :
01-04-2025
Job Description
Location: Allschwil, Switzerland
Schedule: Full-time 100
Duration: 12 months
Start Date: ASAP
Are you a medical professional with a passion for clinical research and drug development? We are looking for a Clinical Trial Physician (CTP) to join our team in Switzerland! This role offers the opportunity to contribute to cutting-edge clinical trials while ensuring compliance with Good Clinical Practices (GCP) and regulatory standards.
Key Responsibilities:
What We re Looking For:
Why Join our client?
Apply:
For more information or to apply please contact Adrien Guimard on Please quote job reference 127 849 in all correspondence.
Schedule: Full-time 100
Duration: 12 months
Start Date: ASAP
Are you a medical professional with a passion for clinical research and drug development? We are looking for a Clinical Trial Physician (CTP) to join our team in Switzerland! This role offers the opportunity to contribute to cutting-edge clinical trials while ensuring compliance with Good Clinical Practices (GCP) and regulatory standards.
Key Responsibilities:
- Develop a deep understanding of the therapeutic area, science, and medicine involved.
- Contribute to writing and amending clinical trial protocols, informed consent forms (ICF), and study reports.
- Provide medical oversight for trials, including safety monitoring, quality assurance, and data review.
- Deliver medical training to the Clinical Trial Team (CTT) and other staff.
- Interpret clinical trial data and interact with external experts, monitoring committees, and regulatory bodies.
- Respond to trial-related questions from Ethics Committees (EC), Institutional Review Boards (IRB), and Health Authorities (HA).
What We re Looking For:
- MD qualification.
- Minimum 4 years of experience in clinical research within the pharmaceutical, biotech, or academic sector.
- Experience in the relevant therapeutic area is a plus.
- Strong knowledge of drug development, clinical trial processes, and regulatory requirements (ICH/GCP guidelines).
- Excellent organizational, analytical, and problem-solving skills.
- Ability to work independently and within a cross-functional team.
- Fluent English skills (written & oral).
Why Join our client?
- Be part of a dynamic team working on innovative clinical research projects.
- Collaborate with leading experts in the field.
- Work in a fast-paced environment where your contributions make a difference.
Apply:
For more information or to apply please contact Adrien Guimard on Please quote job reference 127 849 in all correspondence.
Employment Type
4
Company Industry
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