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CTA
- Permanent
- Clinical Trial Assistant (CTA)
- Switzerland
This vacancy has now expired. Please see similar roles below...
A commercial-stage medical device manufacturer is seeking to hire a Clinical Trial Associate (CTA) to their office in Switzerland. The organisation develops novel, proprietary therapies for treating cancer and tumour. With offices spanning across Europe, Asia, and the U.S., this is an exciting company to work with and provide invaluable support to their team.
Job Responsibilities:
- Becoming involved in various tasks to support the Study Team/Management with any trial related activities in all phases of the conduct of the clinical trial.
- Assisting in the preparation of study specific tools (including communication tools such as study specific websites, newsletters, flyers etc.).
- Supporting the CTM in the setting-up and maintaining study specific trackers to ensure continuous oversight of the study progress.
- Managing all study-related supplies.
- Preparing study reports, keeping required tools, tracking databases up to date as required.
- Ensuring that clinical trials are conducted in accordance with the protocol, Good Clinical Practice regulations, and internal Standard Operating Procedures.
- Performing ongoing quality checks/reviewing documents for the Trial Master File and following up.
- Supporting the CTM in preparing for -and following up after- site, vendor, or sponsor audits and inspections.
Skills and Requirements:
- Bachelor's degree in Nursing, Medicine, or other Life Sciences, or an RN degree from an accredited school.
- Minimum of 2 years of experience of clinical trial management (experience as CRA is an advantage)
- Knowledge of ICH/GCP guidelines (accredited GCP course desirable).
- Experience in identifying potential deficiencies in the trial progress and assisting in/suggesting corrective and preventive actions (CAPA).
- Demonstrable multitasking, project management, and execution skills.
- Good interpersonal skills, including communication, presentation, persuasion, and influence.
- Good organisational skills, including efficiency, punctuality, and collaboration in a team environment.
- Proficiency with computer skills, such as MS Office.
To Apply:
Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please contact Julia Tegelmann at +44 203 854 1052 or upload your CV on our website - www.proclinical.com.
A full job description is available on request.
Proclinical Staffing is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
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