Jobs 11 bis 20 von 265 (dupliziert 225)
Aplitrak - Sevenig (Our)
Representing the company on teams for assigned products/programs; -Collaborating with partners to ensure coordinated safety reporting activities; Participating in the review and interpretation of clinical trial results ( toVor 60+ Tage
Aplitrak - Sevenig (Our)
regulations and guidelines Extensive work in clinical development and trial design. English fluent, German not needed but preferred Preferred previous work in the clinics, ideally with cancer patients. Proven trackVor 60+ Tage
Global Director Clinical Operations (PR/270611) Leip...
Aplitrak - Leipzig
project goals in a timely and accurate manner Represent the clinical trial programs at regulatory authority meetings, cross-functional internal meetings, sales and management meetings Be responsible for implementing andVor 60+ Tage
Packaging & Labeling Specialist (m/w/d) (RE
Aplitrak - Marburg an der Lahn
management experience. Professional experience of 5+ years with at least 3-4 years in clinical supply management, clinical logistics or R&D project management Competencies Very good understanding of clinical trial Vor 60+ Tage - Preview
Karrierezentrum - Frankfurt
The project will be dedicated to the further development of CAR-NK cell therapy, which is a main focus at the site and is currently being tested in a first therapy study in patients within the CAR2BRAIN trial . Preclinical workVor 60+ Tage
StellenMarkt - Marburg an der Lahn
Erfahrungen im Bereich Clinical Trial Supplies und in der Leitung von globalen Studien Kenntnisse und Erfahrungen in GCP/GMP/GDP einschließlich relevanten Standards, regulatorischen Anforderungen und Regularien bezogen aufVor 60+ Tage - Preview
Aplitrak - Sevenig (Our)
clinical, and post-marketing safety data Review and interpret the safety portion of clinical trial reports Provide guidance to product/program teams and CROs for safety case review and adjudication. As a Head ofVor 60+ Tage
Stellenangebot Group Product Safety Manager
StellenMarkt - Sevenig (Our)
Principle contact with regulatory content provider Ensure SDS requirements for R&D and trial products are generated in accordance with the required regulations Ihr Profil Bachelor or Master degree in Chemistry orVor 60+ Tage - Preview
Drug Safety Physician - FREELANCE (PR-33258851) Baye...
Freelance - Bayern
PSURs, DSURs, RMPs and SDRs Preparation of submission documents for marketing authorization applications (MAA) requested by EU authorities Performs triage of incoming cases of (ICSRs) and clinical trial serious adverseVor 60+ Tage
Clinical Contracts Specialist Pharma (W/M/N)
Aplitrak - München
Biologie, Onkologie, Orphan, drug, Master, Bachelor, GCP, GxP, Clinical, CRO, Studien, klinisch, TMF, Prüfplan, Prüfbogen, Monitor, CRA, CTA, Clinical Research Associate. Trial Master File; GCP, GxP, Clinical, Contracting Vor 60+ Tage - Preview