Clinical Trial Manager Jobs in Basel
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Search Results - Clinical Trial Manager Jobs in Basel
ITJOBS-Basel
Clinical Trial Manager m/f/d, Basel-Stadt The Clinical Trial Manager serves as their region's lead and expert on complex clinical development trials to secure expeditious country level set-up, start, enrolment and quality controlContract duration...
CTC Resourcing Solutions-Basel
and will be responsible for the end-to-end management and reporting of safety cases from clinical trials in compliance with applicable regulatory requirements and internal procedures.
Main Responsibilities
Manage the complete lifecycle of safety cases including triage...
ITJOBS-Basel
for the collection and delivery of clinical trial samples (e.g. Safety, Chemistry, Biomarker, PK and PD) across the portfolio of trials. The BOL is an integral part of the Clinical Trial Team and provides operational/ project management expertise as it relates...
F. Hoffmann-La Roche Gruppe-Basel
manager status
• Closely interface with project team leaders as well as safety, clinical pharmacology, clinical operations, biostatistics, regulatory, research and biomarker groups and other members of project teams
• Lead and/or support internal...
appcast.io -
IQVIA Laboratories-Basel
IQVIA Laboratories in Basel is seeking an Associate Director Quality - Client Dedicated Process & QD Manager. This role involves process management, document oversight, and supporting clinical trials in accordance with GDO standards.
Candidates...
Abbott Laboratories-Basel
to PSURs, clinical overviews, and risk management plans
• As part of the Labeling Sub‑Team, provide medical input and scientific strategies for global and national label changes, including safety‑related updates
• Ensure that all medical and promotional...
appcast.io -
Indivi-Basel
and according to relevant regulatory requirements and internal QMS and ISMS requirements.
Accountability for all aspects of risk management oversight (e.g. business, clinical, product, security) as part of a centralised risk- register.
Collaborate with process...
Elan Personal AG-Basel
to release pharmaceutical products for clinical trials, and finally for commercial supply. The QC-Section within the Analytical Development Department is responsible for the Release of Materials based on the GMP compliant execution of Analyses of Inprocess...
Granite Bio-Basel
Oversee data management activities for Phase I trials with emphasis on complex and exploratory datasets
Define and enforce data standards, structures, and validation rules (e.g., CDISC where applicable)
Review key documents (DMPs, CRFs, data transfer...
Abbott Laboratories-Basel
Act as a core member of the Product Safety Team, overseeing medical safety monitoring and contributing to PSURs, clinical overviews, and risk‑management plans
• As part of the Labeling Sub‑Team, provide medical input and scientific strategies...
appcast.io -
IQVIA Laboratories-Basel
of experience in clinical development in pharmaceutical industry or CRO or equivalent including at least 5 years direct involvement in sponsor – CRO interaction for global trials.
Experience in different functions in the clinical development area.
Experience...
Coopers Group AG-Basel
for the collection and delivery of clinical trial samples (e.g. Safety, Chemistry, Biomarker, PK and PD) across the portfolio of trials. The BOL is an integral part of the Clinical Trial Team and provides operational/ project management expertise as it relates...
stellen-basel.ch -
Roche-Basel
the delivery of these roadmaps. This includes securing governance endorsement and resourcing; leading CoE matrix team delivery; managing vendor/technology partnerships; ensuring seamless integration of sensor-based DHTs into clinical trials, including study...
roche.com -
Basel
Coordinate the preparation, submission, management and maintenance of regulatory submissions related to clinical and non‑clinical development activities, including but not limited to:
• Clinical Trial Applications (CTAs)
• Submissions...
michaelpage.ch -
Basel
Overall accountability for drug supply chain in preclinical and clinical trials.
Qualifications:
• PhD or MSc in Organic or Analytical Chemistry, Pharmaceutical Chemistry, Pharmaceutical Sciences or related scientific discipline.
• Two (for PhD) or five...
icims.com -
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