Clinical Trial Manager Jobs
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Search Results - Clinical Trial Manager Jobs
BeOne MedicinesBasel
quality standards, within timelines and budget
Builds solid knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager
Supports the alignment of regional deliverables with overall study goals under...
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...
BeiGeneBasel
BeOne in Switzerland seeks an experienced Regional Trial Support professional to assist the Regional Clinical Study Manager in delivering regional studies on time and within budget. You will build knowledge of clinical trial operations while...
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...
BeOne MedicinesBasel
BeOne Medicines seeks an experienced Regional Trial Support professional to assist the Regional Clinical Study Manager in regional study delivery in Switzerland. You will help with feasibility, study setup, documentation, tracking of samples...
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...
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...
Neurocrine BiosciencesAllschwil
needs.
The role requires extensive experience in drug development, regulatory strategy, and trial design, with a track record guiding projects through global regulatory submissions and risk management.
#J-18808-Ljbffr...
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...
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...
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...
BeiGeneBasel
across clinical trials. The role provides leadership and oversight to ensure consistent implementation of GCP and regulatory requirements, effectiveinspectionreadiness programs, and successful management of inspections and audits.
Key responsibilities...
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
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
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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