Clinical Trial Physician - 12 month contract - Switzerland
Location | Switzerland |
Discipline: | Clinical Development |
Job type: | Contract |
Salary: | £77.96 CHF p/h |
Contact name: | Harry Henson |
Contact email: | harry.henson@rbwconsulting.com |
Contact phone: | +441293364092 |
Job ref: | CTP2003 |
Published: | 8 months ago |
Duration: | 12 months |
Expiry date: | 20 Apr 2024 10:59 |
Startdate: | ASAP |
RBW Consulting are partnered with a global Biopharma who specialise in the discovery, development and commercialization of innovative small molecules, with the aim of transforming the horizon of therapeutic options, in their search for a Contract Clinical Trial Physician.
The Clinical Trial Physician will play a key role in a large global phase 3 cardiovascular outcome study. In addition to the responsibilities described below, the CTP will be specifically responsible for the implementation of the study-specific patient training strategy. The tasks and activities of the Clinical Trial Physician will be carried out in close collaboration with the study Clinical Trial Scientist, the Clinical Lead and Cardiovascular Medical Expert.
This role is for 1 FTE on an initial 12 month contract, with 1-2 days per week in the Allschwil office. The rate for this position is CHF 77.96 per hour.
Responsibilities
Providing the medical leadership internally for the trial activities assigned, through a comprehensive understanding of the science, medicine, product environment and competitive landscape relating to a disease area
Delivering the medical aspects of the Clinical Project Development Plan related to the indication and overseeing its implementation
Contributing 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
Supporting the Clinical lead by contributing to global strategic development and providing evidence-based input to clinical project-related, strategic and regulatory documents
Writing protocol amendments and other study related documents such as the Informed Consent Form (ICF), committee(s) charter(s), subject narratives and the Clinical Study Report (CSR)
Delivering medical oversight of the study (including safety, medical review of data during the trial, quality and performance of the trial)
Interpreting Clinical Trial data and present conclusions and action plan(s) to Clinical Development Management team
Managing contacts with external Experts, National Coordinating Trainers (NCTs) and study site investigators
Answering to trial-related EC/IRB and HA questions
Developing a sound understanding of the science and medicine relating to the therapeutic area
Developing a sound understanding of the complexity of global clinical development with an attention to methodological and ethical aspects of development, in the assigned therapeutic area
Performing literature reviews and write position papers as necessary
Delivering medical training to the study teams’ members and staff and protocol-related training to study sites
Requirements
MD
At least 2 years’ experience in clinical research in a Pharmaceutical and/or Biotech company or equivalent in Academia preferably within cardiovascular therapeutic area
Experience in patient education is a plus
Good knowledge of drug development and clinical trial process based on previous experience
Good knowledge of regulatory requirements/ICH guidelines
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
Results driven attitude and good sense of urgency
Able to anticipate and proactively address issues and demands, solution oriented and hands-on
Analytical thinking, data and detail oriented
Shares knowledge and expertise openly
Excellent written and spoken communication skills in English
Please apply here and Harry Henson will be in touch to discuss your application further!
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