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Clinical Trial Manager Jobs

1 - 15 of 117
1 - 15 of 117
Search Results - Clinical Trial Manager Jobs
CDR-Life AG-Horgen
The Clinical Trial Manager directs and/or supports the planning and management of clinical trials in an outsourced environment. The role is responsible for effective CRO and vendor management and oversight, supports and conducts co-monitoring...
Michael Page (Switzerland)-Geneva
Strong experience negotiating and managing:  •  Clinical Trial Agreements (CTAs)  •  CRO Agreements  •  Research-related agreements  •  Data Protection and Privacy Agreements  •  Demonstrated experience working on multi-jurisdictional matters within...
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Interiman group - Flexsis-Allschwil
Functieomschrijving Description of the company The Trial Data Manager leads end-to-end Data Management activities for assigned clinical trials, ensuring high-quality, consistent data delivery in line with internal standards, applicable regulations...
gloor&lang AG-Basel
 12.  month temporary assignment | Basel | Global Pharmaceutical Company For a global pharmaceutical company in Basel, we are looking for an experienced Senior Clinical Outcomes Assessment (COA/PRO) Manager with strong expertise in patient-centered...
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IQVIA-Zurich
Clinical Trial Psych Rater - German Speaking Location: Remote/Virtual Hours: Estimated 10–16 hours per month Role: Clinical Specialist About IQVIA IQVIA is a global leader in advanced analytics, technology solutions, and clinical research...
2 similar jobs: Basel, Eysins
Rivia-Zurich
science, technical account management, or similar roles.  •  Scientific and technical fluency: You understand scientific data and experimental logic, and can quickly grasp complex clinical trial workflows and technical requirements.  •  Hands‑on technical...
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Adecco-Basel
trials Strong ability to develop and implement tactics for optimal clinical outcome strategy Understanding of regulatory and HTA requirements in global healthcare environments Experience working within cross-functional and international project teams...
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CTC-Basel
representative for clinical study teams, ensuring trial execution complies with international regulations, protocol specifications, and ethical standards across all participating sites and trial partners.  •  Oversee and conduct GCP audits, including clinical sites...
Adecco-Basel
Shape the future of patient-centered drug development For our client, a global leader in the life sciences industry, we are looking for an experienced Senior HEOR Manager to drive Clinical Outcome Assessment (COA) strategies across international...
BeiGene, Ltd.-Schweiz
Excel, PowerPoint) **Preferred Qualifications:*** Certification in GCP auditing or clinical research is a plus.* Experience working with electronic Trial Master File (eTMF) and Clinical Trial Management Systems (CTMS).* Familiarity with risk-based...
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Adecco-Basel
Shape the future of patient-centered drug development For our client, a global leader in the life sciences industry, we are looking for an experienced Senior HEOR Manager to drive Clinical Outcome Assessment (COA) strategies across international...
IQVIA Inc-Zug
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence. We oversee complex budgets and negotiate trial agreements on a global scale. The role is Hybrid in Zug, Switzerland, focusing...
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ITech Consult AG-Zug
tracking, and biobanking workflows according to standard operating procedures (SOPs).  •  Proven track record managing clinical trial operations, protocols, and deliverables from study start-up to completion, adhering to defined project timelines, milestones...
Alentis Therapeutics-Allschwil
expertise in global clinical trial leadership, clinical data review and signal detection, project management, and risk management.  •  Strong understanding of the oncology drug development continuum from First-in-Human (FIH) through late-stage clinical...
ITech Consult AG-Rotkreuz
according to standard operating procedures (SOPs).  •  Proven track record managing clinical trial operations, protocols, and deliverables from study start-up to completion, adhering to defined project timelines, milestones, and scope.  •  Strong working knowledge...
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