Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
C115 (FCRS = CH115) Sandoz Pharmaceuticals AGRotkreuzappcast.io
Sandoz Pharmaceuticals AG in Switzerland seeks a Medical Manager to design, implement and execute Medical Affairs plans for the assigned therapy area, aligning with product strategy.
You will provide scientific information, contribute to clinical...
AXEPTA SAGeneva
of evidence: IFU, risk management files, PMS data, trials and tests, labelling, complaints, vigilance and scientific literature.
• Ensure the alignment of clinical data within all regulatory documentation.
• Train and support the external providers involved...
Roche Holding AGBaselappcast.io
in the pharmaceutical/healthcare industry and drug development (therapeutic area a plus), alongside a solid understanding of the clinical trial environment, ICH‑GCP, and lifecycle sequence/interdependencies.
• You are highly experienced in clinical trial management...
SJP Biotec GmbHZurich
development field - RAS/eIF4A/translation-pathway inhibition.
Key Responsibilities
Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
Lead and manage all clinical development activities...
DebiopharmLausanneappcast.io
Mission
The Clinical Development Quality Manager (CDQM) is responsible for ensuring quality oversight across clinical development activities and supporting the maintenance of GCP compliance. This role supports stakeholders in vendor qualification...
headcount AGZurich
headcount AG in Switzerland seeks a Group Lead Clinical Operations to guide a growing team of Clinical Project Managers and shape the clinical development strategy. You will oversee global Phase I/II trials, ensure on-time delivery within budget...
Alentis TherapeuticsAllschwiljoin.com
management:
• Develop demand forecasts and supply plans based on study protocols, clinical scenarios and enrollment projections.
• Plan, implement and execute the supply strategy for trial medication and ancillary supplies in collaboration with clinical...
headcount AGZurich
biotechnology or pharmaceuticals
• Extensive experience managing global Phase I and/or II clinical trials
• Previous experience leading Clinical Project Managers or cross‑functional clinical teams
• Strong understanding of clinical development strategy
• Proven...
SJP Biotec GmbHZurich
Key Responsibilities
• Translate and deliver key directives from the board and senior management, and serve as the clinical face of the company.
• Lead and manage all clinical development activities across the SJP portfolio
• Design Phase 2 and 3...
GSKBaar
clinical studies, including real-time clinical decision-making on patient eligibility, protocol-related medical queries, and safety oversight
Conduct and oversee medical review of clinical trial data, both directly and through oversight of delegated medical...
Johnson & Johnson Innovative MedicineAllschwil
documents, including:
• Risk management plans.
• Safety development plan.
• Clinical Trial Protocols and Informed Consent Forms (ICF).
• Safety sections of Investigator's Brochure (IB) and addenda.
• Clinical Study Reports (CSR).
• Annual Safety...
IncyteMorges
clinical trials.
Identifies, evaluates, and proactively manages clinical and program risks, implementing mitigation strategies to support program success.
Represents the organization at scientific and medical forums, including congresses, advisory boards...
CSL Plasma Inc.Zurichappcast.io
CSL Plasma Inc. is seeking a senior scientific leader to provide input to clinical development strategies and trial design in Glattbrugg, Switzerland.
The role drives the scientific strategy across programs, authors key study documents, and mentors...
IncyteMorges
Incyte is seeking a senior clinical development leader to implement early development programs for dermatology, immunology, and rheumatology assets. This role involves shaping translational strategies, coordinating cross-functional teams, managing...
CSL Plasma Inc.Zurichappcast.io
the highest quality and full compliance of all outputs. Will contribute to the development of the scientific strategy of the clinical development plan, the design of trial‑related documents and the scientific oversight of clinical trials.
You will facilitate...
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