Clinical Trial Scientist
Posted 5 days 11 hours ago by CK Group
Permanent
Full Time
Other
Not Specified, Switzerland
Job Description
Now Hiring: Clinical Trial Scientist
Location: Allschwil, Switzerland
Schedule: Full-time (100%)
Start Date: ASAP
Duration: 12 months
Are you an experienced Clinical Trial Scientist looking for an exciting opportunity to contribute to cutting-edge clinical research? Join our team in Switzerland and be part of a global organization driving innovation in drug development.
Key Responsibilities:
What We re Looking For:
Why Join Our Client?
If you're ready to take on this exciting challenge, apply today and be part of a company shaping the future of healthcare!
Apply:
For more informaiton or to apply for this role please contact Rob Angrave at CKQLS. on . Please quote job reference in all correspondence.
Location: Allschwil, Switzerland
Schedule: Full-time (100%)
Start Date: ASAP
Duration: 12 months
Are you an experienced Clinical Trial Scientist looking for an exciting opportunity to contribute to cutting-edge clinical research? Join our team in Switzerland and be part of a global organization driving innovation in drug development.
Key Responsibilities:
- Collaborate closely with Clinical Trial Physicians (CTPs) on trial-related activities.
- Develop a strong understanding of the science and medicine behind the trial.
- Perform literature searches to stay updated with the latest research.
- Contribute to the creation of clinical trial documents, including protocols, informed consent forms (ICFs), study guidelines, and clinical study reports (CSRs).
- Provide scientific input and review cross-functional trial documents such as statistical analysis plans (SAPs) and monitoring guidelines.
- Conduct medical monitoring and data review during the trial.
- Participate in discussions with external experts and regulatory bodies.
- Deliver training on the scientific aspects of the trial to relevant teams.
What We re Looking For:
- PhD, PharmD, MSc, or equivalent in life or health sciences.
- 2-5 years of experience in clinical development within a CRO or pharmaceutical company.
- Experience in Phase II & III clinical trials (planning, setup, conduct, and reporting).
- Strong understanding of GCP, ICH guidelines, and regulatory requirements in clinical trials.
- Excellent organizational, analytical, and problem-solving skills.
- Ability to work independently and within a cross-functional team.
- Fluent English skills (written & oral).
- Willingness to travel occasionally as needed.
Why Join Our Client?
- Work with a dynamic, cross-functional team at the forefront of clinical research.
- Contribute to life-changing medical innovations.
- Opportunity to develop expertise in global clinical development.
If you're ready to take on this exciting challenge, apply today and be part of a company shaping the future of healthcare!
Apply:
For more informaiton or to apply for this role please contact Rob Angrave at CKQLS. on . Please quote job reference in all correspondence.