Clinical review Jobs
76-100 von 152 Jobs
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- Ausbildung
- Befristet
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- Nebenjob
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- Unbefristet 1
- Teilzeit 1
- Vollzeit 12
- Innerhalb der letzten 24 Std. 22
- Innerhalb der letzten 7 Tage 114
-
Manager / Sr Manager Regulatory Operations Europe
Incyte Corporation Morges, Waadt
...other duties and/or special projects as assigned or required. Duties and Responsibilities. Responsible for the timely planning, compiling, publishing, review...
vor 7 Tage in JobleadsMelden -
Technical Writer
Envista Kloten, Zürich
...Authoring Case Studies: Collaborate with internal teams and external clinicians globally to develop compelling case studies that highlight the clinical...
vor 3 Tage in Talent.comMelden -
Manager / Sr Manager Regulatory Operations Europe
Incyte Corporation Bern, Bern
...other duties and/or special projects as assigned or required. Duties and Responsibilities. Responsible for the timely planning, compiling, publishing, review...
vor 7 Tage in LifeworQMelden -
Senior Manager, Global Marketing
Bio-Techne Bern, Bern
...for events, as well as collateral and tools to support the Commercial Team efforts. Lead, supervise and review the Marketing Operations activities, including
vor 6 Tage in LifeworQMelden -
Analytical Development – Quality Control Manager (6519)
CTC Resourcing Solutions Basel, Basel-Stadt
...review for reporting to finance and management. Establishment of source documents for IND, IMPD, and NDA/MA submissions as well as responding to agency...
vor 6 Tage in LifeworQMelden -
Manager Regulatory Affairs and CMC (m/f/d)
CARBOGEN AMCIS Bubendorf, Basel-Landschaft
...In this very dynamic and hands-on role, you will work collaboratively with the other departments to coordinate the regulatory activities from clinical...
vor 6 Tage in LifeworQMelden -
Audit Specialist
AdaptHealth LLC Fully, Wallis
...necessity documentation. Job Duties: Develop and maintain working knowledge of current HME products and services offered by the company. Maintain and review...
vor 7 Tage in JobleadsMelden -
Manager RAC (Regulatory Affairs and CMC) (m/f/d)
CARBOGEN AMCIS Bubendorf, Basel-Landschaft
...in terms of change management (change controls, deviations) CMC regulatory support during the entire process and product development from the pre-clinical...
vor 3 Tage in Talent.comMelden -
Senior Manager, Regional Regulatory Affairs
Novocure Baar, Zug
...Optune, is approved for the treatment of adult patients with glioblastoma (GBM) in the USA, Europe and Israel. Novocure has ongoing or completed clinical...
vor 6 Tage in LifeworQMelden -
Manager QA GMP (m/f/d)
Tubulis GmbH Lausanne, Waadt
Be part of our team We are a dedicated QA team supporting Tubulis development of antibody-drug conjugates (ADCs) and clinical trials with a strong focus on...
vor 2 Tage in LifeworQMelden -
Senior Manager, Regional Regulatory Affairs
Novocure Baar, Zug
...Clinical, R&D, and Marketing teams to align regulatory strategy with business goals. Serve as a mentor or technical resource to junior team members, without...
vor 7 Tage in LifeworQMelden -
R&D Technology Project Manager (1818_92169)
Medacta Italia Rancate, Tessin
...review linked to performance and professional development; continuous training. Medacta International is an equal opportunity employer. Qualified applicants...
vor 7 Tage in LifeworQMelden -
QA Manager - Computerized Systems Validation (CSV)
F. Hoffmann-La Roche Gruppe Kaiseraugst, Aargau
...This role includes oversight of quality assurance tasks in both commercial DS (Drug Substance) and DP (Drug Product) production as well as clinical...
vor 5 Tage in JobleadsMelden -
Regulatory Affairs Specialist - Mendrisio site (Ticino)
neu Sintetica Mendrisio, Tessin
...improve therapies by enhancing its products' formulations and usability for the benefit of clinicians and patients. We do so in close cooperation with clinical...
vor 18 Std. 26 Minuten in Talent.comMelden -
R&D Technology Project Manager
Medacta International Rancate, Tessin
...review linked to performance and professional development; continuous training. Medacta International is an equal opportunity employer. Qualified applicants...
vor 7 Tage in LifeworQMelden -
Technical Writer
Medimaps Group Genf, Genf
...Review of Installation guides to the high-quality level and standards required in collaboration with Developers for creation of technical content. Support...
vor 3 Tage in LifeworQMelden -
Legal Counsel 80-100% (8-month Limited Contract) - Geneva
Ompharma Genf, Genf
...advice internally for all contractual matters and operational activities, relating in particular to medical affairs, marketing, regulatory, safety, clinical...
vor 7 Tage in LifeworQMelden -
Associate Director, Health Economics and Outcome Research, S
BeOne Medicines Basel, Basel-Stadt
...clinical development) and external KOLs. Represent BeOne at appropriate scientific, medical and payer meetings. Manage external vendors across HEOR projects...
vor 3 Tage in LifeworQMelden -
Academic Mentor
neu Viswin Global Solutions Pvt. Ltd.
...review, mentorship, research collaboration). Equal Opportunity: NexSphere welcomes applications from all qualified individuals regardless of background or...
vor 1 Tag in JobleadsMelden -
Regulatory affair manager
Approach People Recruitment Lausanne, Waadt
...or other regulatory filings, as required. Liaise with regulatory agencies, such as the FDA, EMA, or other regulatory authorities, to facilitate the review...
vor 4 Tage in Talent.comMelden -
Associate Safety Director
F. Hoffmann-La Roche Gruppe Basel, Basel-Stadt
...clinical trial lifecycle. Exhibit excellent communication skills, both written and verbal, capable of effectively collaborating with remote partners on a...
vor 2 Tage in LifeworQMelden -
Associate Director, Health Economics and Outcome Research, S
BeiGene Basel, Basel-Stadt
...clinical development) and external KOLs. Represent BeOne at appropriate scientific, medical and payer meetings. Manage external vendors across HEOR projects...
vor 3 Tage in LifeworQMelden -
QA Manager - Computerized Systems Validation (CSV)
Roche Basel, Basel-Stadt +1 Standort
...This role includes oversight of quality assurance tasks in both commercial DS (Drug Substance) and DP (Drug Product) production as well as clinical...
vor 3 Tage in LifeworQMelden -
Head of Legal & Compliance Europe
Acadia Pharmaceuticals Zug, Zug
...affairs materials and activities, including congress materials, e... symposia and booth content. Review and approve regional and country Expanded Access
vor 3 Tage in LifeworQMelden -
HR Ops & People Partner
Hilo Neuenburg, Neuenburg
...by our founders at the Swiss Center for Electronics and Microtechnology (CSEM). Hilo by Aktiia's solution has been validated through extensive clinical...
vor 3 Tage in JobleadsMelden
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