Clinical Trial Physician
3 days left
- Company
- CTC Resourcing Solutions
- Location
- Canton of Basel-Stadt (CH)
- Salary
- Competitive
- Posted
- 04 Feb 2021
- Closes
- 06 Mar 2021
- Discipline
- Medical Affairs, Clinical Research Physician
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Management
Our client, an innovative and dynamic bio-pharmaceutical company headquartered in Switzerland, is looking for a Clinical Trial Physician based in Basel, Switzerland.
Main Responsibilities:
- Providing medical leadership internally for the trial activities assigned, through a comprehensive understanding of the science, medicine, product environment and competitive landscape
- Delivering medical aspects of the Clinical Project Development Plan related to the indication and overseeing its implementation
- Actively contributes to the core medical/scientific information required in all clinical documents of the respective trial (e.g. protocols, core informed consent forms, clinical study reports, safety related documents etc.) and assure production of high-quality documents
- Responsible of writing the clinical trial protocol including amendments and related documents such as the Informed Consent Form (ICF), committee(s) charter(s), subject narratives and the Clinical Study Report (CSR)
- Ensure that the Case Report Form is designed to allow careful and comprehensive collection of data
- Deliver medical oversight of the study (including safety, medical review of data during the trial, quality and performance of the trial)
- Interpret Clinical Trial data and present conclusions and action plan(s) to Clinical Development Management team as medical representative of the Clinical Trial Team
- Manage contacts with external Experts, Steering Committees (SC), Independent Data Monitoring Committees (IDMC), and other study or project committees.
- Answer to trial-related EC/IRB and HA questions
Qualifications and Experience:
- At least 5 years’ experience in clinical research in a Pharmaceutical or Biotech
- MD
- Good knowledge of drug development and clinical trial process based on previous experience
- Good organizational and communication skills, able to work as part of a team and independently
- Proven record of successfully engaging and interacting within a complex and challenging matrix organization as well as with all levels of seniority
- Analytical thinking, data and detail oriented
- Shares knowledge and expertise openly
- Excellent written and spoken communication skills in English
- Relevant working/residency permit