Regulatory Affairs Manager / Clinical Trial Applications
Frankfurt am Main
Vollzeit
Proclinical Staffing
Proclinical are recruiting a Regulatory Affairs Manager / Clinical Trial Applications for a global pharmaceutical organisation on a permanent basis … Proclinical are recruiting a Regulatory Affairs Manager / Clinical Trial Applications for a global pharmaceutical … Proclinical are recruiting a Regulatory Affairs Manager / clinical Trial Applications for a global pharmaceutical organisation on a permanent …Regulatory Manager Trial StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d)
München
Vollzeit
MSD
… Supporting budget/finance aspects, for execution and oversight of clinical trial country submissions and approvals. Responsibilities include, but are not … partnership internally with GCTO country operations, finance, regulatory affairs, pharmacovigilance, legal and regional operations, HQ functional areas … Our Clinical Research and Pharmacovigilance team push the boundaries of global …Regulatory Affairs Manager Clinical TrialManager Regulatory Affairs CMC Authoring
Mainz
Vollzeit
BioNTech AG
… Extensive experience in authoring of regulatory CMC documents for clinical trial applications (e.g., quality parts of INDs/IMPDs) and/or marketing … hope for a healthy future in many people's lives. Manager Regulatory Affairs CMC Authoring You will author global quality regulatory documents and … Extensive experience in authoring of regulatory CMC documents for clinical trial applications (e.g., quality parts of INDs/IMPDs) and/or marketing …Regulatory Clinical Trial
Associate Director, Field Medical Advisor, Northern Germany
Home Office
Vollzeit
Moderna
… narratives across Moderna’s therapeutic areas, including clinical trial data and research findings, to support the medical and scientific … Scientific Discipline Required Minimum of 4 years of experience in Medical Affairs or field medical roles Here’s What You’ll Bring to the Table (Preferred … scientific narratives across Moderna’s therapeutic areas, including clinical trial data and research findings, to support the medical and scientific …Affairs Manager Trial ApplicationsGlobal Medical Advisor Immunoassay F/M/NB
Nürtingen
Vollzeit
bioMérieux Deutschland GmbH
… hospital/clinical/medical issues and environment; experience in clinical trial management and design, reimbursement environment, regulatory affairs. … culture. What are your accountabilities? Reporting to the Global Medical Affairs Director in charge of immunoassays, and as part of a team of nine people, … within the company for specific medical areas. Provide medical input to clinical trials: investigator and site identification, protocol writing and review, …Regulatory Applications StellenangeboteProcurement Lead Clinical Development (f/m/d)
Aachen
Vollzeit
Grünenthal
… up to executive level, act in this role primarily for clinical trial services and support all other categories in the R&D Development area … and support all other categories in the R&D Development area (e.g. Reg. Affairs, Drug Safety, CMC, CTS, Data Science, etc.) Gain and deliver on a … global stakeholders up to executive level, act in this role primarily for clinical trial services and support all other categories in the R&D Development …Regulatory Affairs Manager TrialSr. Medical Education Specialist (m/w/d)
Mainz
Vollzeit
Dexcom
… at Dexcom, you will facilitate the promotion of emerging clinical trial data, do researches to expanded indications, support strategic … with great clinical and medical communication skills to join our Medical Affairs team in DACH. Bring your experience of educating and treating people with … 9.000 Mitarbeiter. Role Summary: We are looking for someone with great clinical and medical communication skills to join our Medical Affairs team in DACH. …Affairs TrialMedical Writer
Freiburg
Vollzeit
Intuitive Surgical
… tracking external and internal information sources and searches for trial information or evidence from other relevant information sources eg … is principally responsible for medical writing needs for Clinical Affairs EMEA. This includes literature searches, analyses, reviews, compilation … minimally invasive care. Job Description Primary Function of Position: The Clinical Literature Specialist is principally responsible for medical writing needs …Regulatory Manager Clinical Applications StellenangeboteClinical Program Lead
Biberach an der Riß
Vollzeit
BI International GmbH
… Asset Evidence Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis and Data Management Plan, … of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific Platform, Publication Plan, Product … at the International Multidisciplinary Evidence Teams and you take clinical development responsibility for the projects assigned. For example: …Regulatory Clinical Trial StellenangeboteSenior Clinical Study Administrator, Country Operations
München
Vollzeit
Alexion Pharmaceuticals,Inc. (gehört zu AstraZeneca)
… Country Operations Management (COM) to ensure quality and consistency of trial deliverables to time, cost and quality objectives according to Good … translations, IRB/CEC/CA submissions in collaboration with Regulatory Affairs and other functions, as required within the country/region. Providing … Reports To: Head of Country Operations This is what you will do: The Clinical Study Administrator (CSA) assists in the coordination of study activities …Affairs Manager ApplicationsCoordinator
Hennigsdorf
Vollzeit
Thermo Fisher Scientific
… that help millions of lives around the world. Coordinator (m/f/d) Clinical Trial Thermo Fisher Scientific Inc. is the world leader in serving science, with … Impactful Work: We are looking for you to strengthen the Global Medical Affairs team of the Biomarker Business Unit as soon as possible. In this position … tools that help millions of lives around the world. Coordinator (m/f/d) Clinical Trial Thermo Fisher Scientific Inc. is the world leader in serving …Affairs Manager Applications StellenangebotePackaging & Labeling Specialist (m/f/d)
Biberach an der Riß
Vollzeit
Randstad Deutschland
… Text drafts considering regulatory requirements, standard text phrases and trial specifics Prepare country specific label text for translation of attending … Autonomously work in conjunction with CTSU Trial teams, Regulatory Affairs, Global Randomization, Medicine and label vendors to create, define and … training with extensive experience in a related field Background in Clinical Trials (Supply Chain, Clinical Trial Regulations, Packaging and Labeling …Regulatory StellenangeboteGlobal Pharmacovigilance Operations Lead (f/m/d)
Garching bei München
Vollzeit
ITM Isotope Technologies Munich SE
… and ICH guidelines, initiatives, and regulations governing both clinical trial and post-marketing safety environments Experience in case processing, … (Clinical Operations, Clinical Science, Data Management, Medical Affairs) and external vendors What we offer: A modern workplace and exciting … training on ICSR activities, safety procedures and processes including clinical and post-marketing regulatory reporting requirements Support and/or …Regulatory Affairs Applications StellenangebotePackaging & Labeling Specialist (m/f/d)
Biberach an der Riß
Vollzeit
Randstad Deutschland
… Text drafts considering regulatory requirements, standard text phrases and trial specifics Prepare country specific label text for translation of attending … Autonomously work in conjunction with CTSU Trial teams, Regulatory Affairs, Global Randomization, Medicine and label vendors to create, define and … training with extensive experience in a related field Background in Clinical Trials (Supply Chain, Clinical Trial Regulations, Packaging and Labeling …Regulatory Clinical Trial Applications