Aktuelle Jobs im Zusammenhang mit Senior Clinical Trial Associate - Basel, Basel-Stadt - headcount AG
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Clinical Document and Trial Master File
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Clinical Document and Trial Master File
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Clinical Operations Manager
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Senior Clinical Operations Lead
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Clinical Operations Project Manager
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Basel, Basel-Stadt, Schweiz gloor&lang AG Vollzeit CHF 80'000 - CHF 120'000 pro JahrAbout the CompanyOur client is an innovative European biotech company advancing novel anti-infective therapies through clinical development. With several programs progressing from Phase 2 to Phase 3, the company is expanding its clinical operations team to strengthen execution, oversight, and cross-functional collaboration in upcoming global studies. About...
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Manager Clinical Supply
Vor 2 Tagen
Basel, Basel-Stadt, Schweiz gloor&lang AG Vollzeit CHF 80'000 - CHF 120'000 pro JahrPermanent | Full-time | Switzerland (Basel Area)We are supporting a growing, innovation-driven biopharmaceutical company in hiring an experienced Clinical Drug Supply Manager to strengthen its Clinical Supply Operations team. As the company expands its global clinical development programs, this newly created position will play a key role in ensuring the...
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Manager Clinical Supply
Vor 2 Tagen
Basel, Basel-Stadt, Schweiz gloor&lang AG Vollzeit CHF 80'000 - CHF 120'000 pro JahrPermanent | Full-time | Switzerland (Basel Area)We are supporting a growing, innovation-driven biopharmaceutical company in hiring an experienced Clinical Drug Supply Manager to strengthen its Clinical Supply Operations team. As the company expands its global clinical development programs, this newly created position will play a key role in ensuring the...
Senior Clinical Trial Associate
vor 2 Wochen
Overview
The Senior CTA supports operational and development activities across assigned clinical studies. This role ensures efficient study execution, high-quality documentation, and effective oversight of CRO vendors and other operational partners. This is a long term contract role to be based in Basel (Hybrid).
Key Responsibilities
- Support study start-up activities, including collection and coordination of essential documents
- Contribute to site and vendor management activities
- Create, manage, and update trackers and logs to ensure oversight of trial progress
- Maintain a high-quality filing structure and oversee archiving of trial documentation
- Oversee and maintain the internal Trial Master File (TMF)
- Conduct regular oversight and quality checks of the external TMF
Qualifications
- Master's degree required
- Experience supporting start-up and later-phase clinical trials
- Strong organizational, documentation, and communication skills
- Ability to collaborate cross-functionally and manage multiple priorities
