Associate Director Global Regulatory Affairs Regulatory Operations Clinical Trials Stellenangebote

Associate Director* Global Regulatory Affairs Regulatory Operations (Clinical Trials) Mainz Vollzeit BioNTech AG … of EU Clinical Trial Application (CTA) submissions in the Clinical Trials Information System (CTIS) in compliance to the EU Clinical Trial … future in many people's lives. Associate Director* Global Regulatory Affairs Regulatory Operations (Clinical Trials) You will define and manage … Trials) You will define and manage Regulatory Operations activities of EU Clinical Trial Application (CTA) submissions in the Clinical Trials Information …Associate Director Global Regulatory Operations Clinical Stellenangebote Medical Scientist (MSL) Liver Diseases (m/f/d) – North-East, (Hamburg, Berlin, Dresden) Hamburg Vollzeit Gilead Sciences … settings. Assists with site selection for both phase 4 and other clinical trials. Anticipates obstacles and difficulties that may arise in the field and … Job Functions An exciting and challenging opportunity to join our Medical Affairs team in Germany has arisen. We are looking for a Medical Scientist (MSL) … experts on various projects and other activities. Assists with Gilead clinical and real-world evidence studies, which includes collaboration with …Associate Director Global Operations Trials StellenangeboteGlobal Medical Advisor Immunoassay F/M/NB Nürtingen Vollzeit bioMérieux Deutschland GmbH … the company for specific medical areas. Provide medical input to clinical trials: investigator and site identification, protocol writing and review, study … 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, …Associate Director Regulatory Affairs Regulatory Operations Clinical

Procurement Lead Clinical Development (f/m/d) Aachen Vollzeit Grünenthal … procurement organization Experience in categories close to clinical trials (e.g. Regulatory Affairs, CMC, CTS, Drug Safety, Medical Writing, … 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 …Associate Director Global Regulatory Clinical Trials StellenangeboteGlobal Head Infection Prevention (m/f/d) Hamburg Vollzeit Olympus Europa SE & Co. KG (OEKG) … product development processes, R&D engineering, risk management, clinical trials, post-market safety surveillance, health hazard assessments and field … Medical Officer, and other senior leaders within Medical and Scientific Affairs to share best practices and ensure consistent patient safety for all … Provide deep expertise, insights, as well as scientific and clinical leadership to IP strategy and strategic decision making while maintaining …Global Affairs RegulatoryAssociate Director Regulatory Affairs Aachen Home Office PAION Pharma GmbH … Management with respect to business needs Working knowledge of EU clinical trials may be useful Good self-management Strong sense of responsibility … Your tasks The Associate Director Regulatory Affairs is responsible for establishing and implementing the regulatory CMC … Cycle Management with respect to business needs Working knowledge of EU clinical trials may be useful Good self-management Strong sense of responsibility …Associate Global Regulatory Affairs Regulatory Clinical Trials StellenangeboteCountry Clinical Operations Manager Germany (all genders) Wiesbaden Vollzeit ABBVIE … Accountable for the on-time and within budget execution of all clinical trials within Germany. Provide local regulatory and legal requirement expertise. … Study Leadership (CSL), Global Study-Start-Up and with Global Medical Affairs (GMA), and other key stakeholders across the organization. Make your mark: … standards in the competitive field. Moving mountains together – as Country Clinical Operations Manager Germany (all genders) in Wiesbaden To enable AbbVie’s …Director Regulatory Affairs ClinicalSenior Clinical Study Administrator, Country Operations München Vollzeit Alexion Pharmaceuticals,Inc. (gehört zu AstraZeneca) … Country Operations (HCO) in delivering support in the conduct of clinical trials in region or country. You will be responsible for: Providing support to … 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 …Regulatory Operations StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d) München Vollzeit MSD … of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and … 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 …Associate Global Regulatory Affairs Regulatory Operations Clinical Stellenangebote Pharmaceutical Scientist - Pharmacovigilance Operations (m/f/d) München Vollzeit Daiichi Sankyo Europe GmbH … Safety & Pharmacovigilance (CSPV) information of ICSR from clinical trials and marketed products. Ensure regional ICSR team compliance with and … to coordinate case processing tasks. Cooperate and support Regulatory Affairs Department with regard to safety aspects during submission and maintenance … (DSE) which focuses on ICSR case handling. Performing Data Management of Clinical Safety & Pharmacovigilance (CSPV) information of ICSR from Clinical trials …Regulatory Operations StellenangeboteCoordinator Hennigsdorf Vollzeit Thermo Fisher Scientific … as possible. In this position you will supervise the conduct of clinical trials at Global Medical Affairs and work closely with national and international … 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 …Global Regulatory Affairs Operations Trials StellenangeboteRegulatory Affairs Manager / Clinical Trial Applications Frankfurt am Main Vollzeit Proclinical Staffing … Responsible for supporting the conduct of sponsored clinical trials of our R&D team to ensure adequate quality and meet regulatory and legal … 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 …Global Affairs Regulatory Clinical TrialsSr. Clinical Project Manager (m/f/d) Deutschland Vollzeit Abiomed … role Expertise with GCP and regulatory compliance guidelines for clinical trials required Solid EU regulatory knowledge including experience with Ethics … the Senior Clinical Program Manager, Clinical Research Associates, Medical Affairs and Regulatory Departments to execute the trial. This role will engage and … commitment to employee professional development. Job Description: The Sr. Clinical Project Manager reports to the Manager, Clinical Programs EMEA and is …Regulatory Affairs Regulatory Clinical Trials StellenangeboteMedical Affairs Advisor Metabolics München Vollzeit AstraZeneca … gastroenterology/hepatologyExperience in the implementation of clinical trials in accordance to ICHGCPProven record in realworld evidence generation … you will do: The Medical Advisor Metabolics is a member of the Medical Affairs Team and will provide scientific and medical leadership especially for … and/or gastroenterology/hepatologyExperience in the implementation of clinical trials in accordance to ICHGCPProven record in realworld evidence …Director Global Regulatory Affairs Regulatory Operations Trials Stellenangebote