NonStop Consulting
Location
Alsace | France
Job description
Clinical Study Disclosure Manager - Join Our Client's Leading Medical Team in Switzerland
Our client, a reputable and fast-growing medical organisation in Switzerland, is seeking a dedicated and experienced Clinical Study Disclosure Manager to join their team in Allschwil. This role offers a unique opportunity to work in a fast-paced and ambitious environment, where expectations are high and personal growth is encouraged. With a diverse workforce representing over 38 nationalities, you will join a team that values individual contributions and fosters a culture of learning and development.
Contract duration: 12 months
Workload: 100%
Start date: ASAP
Benefits:
- Access to a wide range of internal and external learning and development programs to enhance your skills and knowledge.
- Collaborate with professionals from diverse cultural backgrounds, creating an inclusive and dynamic work environment.
- Be part of an organization that embraces innovation and invests in cutting-edge technology and research.
Responsibilities:
- Lead and execute clinical trial disclosure and transparency activities, ensuring compliance with global clinical transparency regulations and company policies.
- Drive the processes for clinical study protocol registration and summary results posting on public clinical trial registries.
- Collaborate with cross-functional teams to plan and execute study disclosure activities, providing guidance and serving as a subject matter expert on best practices.
- Lead transparency initiatives, such as lay language results summaries and clinical data sharing.
- Identify opportunities to improve systems and processes, and lead process improvement initiatives for disclosure and transparency.
Requirements:
- Preferably, hold a higher degree in medical or life sciences, although other scientific degrees associated with pharmaceutical industry experience will be considered.
- Minimum of 5 years' experience in the pharmaceutical industry or related to the conduct of clinical trials.
- Solid understanding of the clinical drug development life cycle, including clinical trial design, operations, and results analysis.
- Demonstrated experience in clinical trial disclosure and transparency processes and systems, with a detailed understanding of global requirements.
- Strong ability to understand, interpret, critically analyze, and summarize complex scientific and medical data.
- Detail-oriented with excellent organizational skills.
- Excellent written and oral communication skills.
- Ability to work independently and as part of a team.
Apply now and we will give you a call to discuss the details of the role.
You can contact me via: [email protected]
Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.
NonStop is one of the largest and fastest-growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Luxembourg, Switzerland, Romania, the US and the Czech Republic and we hold labour leasing licences across Switzerland.
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