Associate Clinical Operations Manager Regulatory Stellenangebote

Clinical Trial Assistant (m|w|d) Bergisch Gladbach Vollzeit Miltenyi Biomedicine … are bringing innovative treatments and reshaping their accessibility for clinical professionals and patients worldwide with the aim to improve and extend … support the preparation and submission of study documents to IRB/IEC and regulatory authorities and assist in the collection or creation and maintenance of … in clinical research as a clinical trial associate, clinical research associate and/or clinical study coordinator in the pharmaceutical/biotech industry. …Manager Regulatory StellenangeboteStudy Start Up Associate I Frankfurt am Main Vollzeit ICON … & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to … and activities. Experience of Clinical Trial operations and meeting regulatory guidelines Proficient project management skills. Benefits of Working in … study start up requirements and activities. Experience of Clinical Trial operations and meeting regulatory guidelines Proficient project management skills. …Associate Clinical Manager Regulatory StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d) München Vollzeit MSD Our Clinical Research and Pharmacovigilance team push the boundaries of global … language Informed Consents and translations. Interact with IRB/IEC and Regulatory Authority for assigned protocols. Manages country deliverables, timelines … to in/directly influence investigators, external partners and country operations and adheres to budget targets and agreed payment timelines. Works in …Clinical Manager Stellenangebote

Associate Director, Account Management München Vollzeit Medpace, Inc. … Maintain a strong relationship with the customer during an ongoing clinical trial; Perform financial analysis and reporting; Oversee client requests … through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, … seeking a full-time, office-based Account Manager to join our Commercial Operations team. This position will work on a team to accomplish tasks and projects …Associate Operations RegulatoryClinical Trial Associate (f/m) Grambach Vollzeit QPS Austria GmbH … successful contract research organization in the preclinical and clinical area. The clinical Research Division handles clinical studies of phases I … payments Assist in the preparation, handling and tracking of Ethics/ Regulatory Submissions in the EU (Clinical Trial Information System) Coordination of … near Graz we are looking for a full-time and office-based Clinical Trial Associate (f/m). Your area of responsibility: The Clinical Trial Associate (CTA) …Associate Manager Regulatory StellenangeboteAssociate Director, Study Start-Up München Vollzeit Medpace, Inc. … in Munich. This position will be an integral part of the Medpace clinical operations management team. This role will be responsible for the … You will also be responsible for providing guidance and expertise to the Regulatory Submissions team in terms of competent authority and IRB/EC/REB … in Munich. This position will be an integral part of the Medpace clinical operations management team. This role will be responsible for the strategic …Associate Operations Manager Regulatory Study Start Up Associate I Home Office Vollzeit ICON ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment … and activities Experience of Clinical Trial operations and meeting regulatory guidelines Proficient project management skills Ability to work … study start up requirements and activities Experience of Clinical Trial operations and meeting regulatory guidelines Proficient project management skills …Associate Regulatory Stellenangebote Clinical Research Associate, sponsor dedicated Home Office Vollzeit ICON The Clinical Research Associate will perform site activities for Phase I-IV studies … investigator site management activities in adherence to all applicable regulatory guidelines and standard operating procedures (SOPs). What you will be … The Clinical Research Associate will perform site activities for Phase I-IV studies operating as the main …Associate Clinical Manager Regulatory StellenangeboteRegional Clinical Trial Management Associate Home Office Vollzeit BeiGene … this position General Description: Role will support the study team with Clinical Operations tasks, and/or assist in ensuring compliance including … activities. Follow TMF Plans, applicable SOPs, ICH/GCP guidelines and regulatory requirements. Support actions ensuring the TMF is submission/inspection … and/or review of Clinical Operations Work Instructions and SOPs The Junior Associate role in Clinical Operations is an entry level position This job …Clinical Operations Manager Regulatory Clinical Project Associate (m/f/d) Global Clinical Operations Frankfurt am Main Vollzeit Merz Therapeutics 5.0 out of 5 YOUR CONTRIBUTION As Clinical Project Associate (m/f/d) you support the conduct of Merz Therapeutics … Therapeutics sponsored clinical trials to ensure adequate quality and meet regulatory and legal requirements. Your detailed tasks are the following: Support … YOUR CONTRIBUTION As Clinical Project Associate (m/f/d) you support the conduct of Merz Therapeutics sponsored clinical …Associate Operations Manager StellenangeboteAssociate Director* Global Regulatory Affairs Regulatory Operations (Clinical Trials) Mainz Vollzeit BioNTech AG … Trials) You will define and manage Regulatory Operations activities of EU Clinical Trial Application (CTA) submissions in the Clinical Trials Information … for a healthy future in many people's lives. Associate Director* Global Regulatory Affairs Regulatory Operations (Clinical Trials) You will define and manage … to be a part of creating hope for a healthy future in many people's lives. Associate Director* Global Regulatory Affairs Regulatory Operations (Clinical …Operations Regulatory StellenangeboteClinical Research Associate - Germany München Vollzeit Translational Research in Oncology … place for you! TRIO (Translational Research in Oncology) is an academic clinical research organization that is dedicated to advancing translational cancer … ICH-GCP and local regulations; Ensuring the completion and collection of regulatory documents; Performing data verification of source documents; Ensuring … of the future to the world of today. We are looking for Clinical Research associates to join our international team, home-based in Germany. Our CRAs play a …Associate Clinical Operations Manager Regulatory StellenangeboteClinical Research Associate ll Deutschland Vollzeit RBW Consulting … to progress your skillset and increase your overall quality as a clinical researcher. It is common for CRAs in Europe to choose this company in … vendors Participate and contribute towards feasibility research Support regulatory department in document preparation for submissions and approval … and have the chance to meet a HR Representative and a member of the Operations Team. Here, you can explore the position and company in more detail to …Clinical Operations Regulatory StellenangeboteJunior Clinical Research Associate München Vollzeit AstraZeneca This is what you will do: The Junior Clinical Research Associate (Jr. CRA) has local responsibility for the delivery of … some countries, as required, CRAs are accountable for study startup and regulatory maintenance; tasks may include collection, preparation, review and … This is what you will do: The Junior Clinical Research Associate (Jr. CRA) has local responsibility for the delivery of the studies at …Associate Operations Manager Regulatory