Clinical Site Monitor I/ II - FSP/ Germany/Homebased
Home Office
Vollzeit
Parexel
… with demonstrated experience in monitoring (virtual or onsite). Oncology trials experience. Experience in utilizing systems like Siebel Clinical Trial … Parexel FSP is hiring for a home-based Clinical Site Monitor I or II. Single sponsor dedicated to a worldwide … where innovation thrives. The Site Monitor will be responsible for data integrity and data quality and will ensure compliance with ICH GCP and …Data Clinical StellenangeboteSenior Clinical Data Manager:in (m/w/d) (Vollzeit, unbefristet)
Deutschland
Vollzeit
DKMS Group gGmbH
… registrierten Spender:innen weiter an diesem Ziel arbeiten. Die Clinical Trials Unit ist die medizinische Forschungsabteilung der DKMS. Die Pflege und der … 12,5 Mio. registrierten Spender:innen weiter an diesem Ziel arbeiten. Die Clinical Trials Unit ist die medizinische Forschungsabteilung der DKMS. Die Pflege … der Clinical Trials Unit in Dresden suchen wir ab sofort eine:n Senior Data Manager:in (m/w/d) im Bereich Klinischer Forschung (Vollzeit, unbefristet) …Data Manager Clinical StellenangeboteClinical Trial Assistant
München
Vollzeit
Translational Research in Oncology
… advanced knowledge in Word, Excel, and PowerPoint. Experience in clinical trials is preferred. Ability to learn new systems and navigate within those … TRIO is a unique, full-service clinical research organization (CRO), dedicated to oncology, that leverages the … preparation. Sending trial materials/documents to the sites. Entering data in the Clinical Trial Management System (CTMS). Ensures appropriate TMF …Data Stellenangebote
Clinical Data Manager:in (m/w/d) (Vollzeit, unbefristet)
Deutschland
Vollzeit/Ausbildung
DKMS Group gGmbH
… registrierten Spender:innen weiter an diesem Ziel arbeiten. Die Clinical Trials Unit ist die medizinische Forschungsabteilung der DKMS. Ein Schwerpunkt … 12 Mio. registrierten Spender:innen weiter an diesem Ziel arbeiten. Die Clinical Trials Unit ist die medizinische Forschungsabteilung der DKMS. Ein … die Betreuung der Zentren suchen wir ab sofort in Dresden eine:n Clinical Data Manager:in (m/w/d) (Vollzeit, unbefristet) IHRE AUFGABEN: • Manuelle …Data Manager Clinical Trials StellenangeboteProcurement 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, … 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 … in the R&D Development area (e.g. Reg. Affairs, Drug Safety, CMC, CTS, Data Science, etc.) Gain and deliver on a comprehensive understanding of …Data Clinical TrialsSr CRA
Home Office
Vollzeit
Thermo Fisher Scientific
… development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks … research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel … actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and …Manager Clinical TrialsClinical Research Associates
München
Vollzeit
Thermo Fisher Scientific
… development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks … research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel … regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships …Manager ClinicalSenior Project Manager Creative Services (f/m/d)
Berlin
Vollzeit
Clariness
… by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster. For more … field of Project Management. Initial understanding of the Life Science or Clinical Trial Industry. Advanced MS Office skills. Great communication and … and will especially observe the applicable provisions of the applicable data protection laws. Further information about the use of the applicant data, …Data Trials Stellenangebote
Clinical Research Associate, sponsor dedicated
Home Office
Vollzeit
ICON
… an independent CRA, including conducting monitoring visits for clinical trials, from either a pharmaceutical company or a CRO environment A working … The Clinical Research Associate will perform site activities for Phase I-IV studies … when appropriate Conduct in-house review of Case Report Forms Assist with data query resolution Perform telephone monitoring activities in order to …Data ClinicalClinical Research Associate (all levels), Oncology, FSP, home based, client dedicated
Home Office
Vollzeit
Syneos - Clinical and Corporate - Prod
… be adjusted to your level). Previous experience with monitoring Oncology trials in Germany Fluent in German and English (verbal and written) and excellent … Description Clinical Research Associate - home based, sponsor dedicated, flexible level based … on-site monitoring & oversight activities using various tools to ensure: o Data generated at site are complete, accurate and unbiased o Subjects' right, …Manager StellenangeboteNegotiation Manager(m/d/w)
Nürnberg
Vollzeit
Novartis
… and also responsible for contract and budget negotiations in clinical trials conducted by SSO with dedicated focus on establishing strong and reliable … accountable and also responsible for contract and budget negotiations in clinical trials conducted by SSO with dedicated focus on establishing strong and … of negotiation outcome e.g. adaption of budget agreements to site master data file Establish database with site specific details to offer site details …Data Trials
Study Start Up Associate I
Home Office
Vollzeit
ICON
… investigational, new pharmaceutical and biological products for clinical trials at their local practices. You will be partnering with one of the worlds … ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment … and status Perform timely and accurate task progress communication and data entry of all relevant study start up activities into the appropriate …Data Manager
Medical Science Liaison (w/m/d) Dermatology & Rheumatology, Gebiet: Hessen/ Thüringen (befristet bis 31.08.2025)
München
Vollzeit
Bristol-Myers Squibb
… perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, … and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, … and conviction records, pursuant to applicable laws in your area. Any data processed in connection with role applications will be treated in …Manager StellenangeboteProject Manager Creatives (f/m/d)
Berlin
Vollzeit
Clariness
… by accelerating medical innovation through improved access to clinical trials, potentially bringing needed treatments to patients faster. For more … field of Project Management. Initial understanding of the Life Science or Clinical Trial Industry. Advanced MS Office skills. Great communication and … and will especially observe the applicable provisions of the applicable data protection laws. Further information about the use of the applicant data, …Clinical Trials Stellenangebote