Postdoc position (f/m/d)
Aachen
Vollzeit
Universitätsklinikum Aachen AöR
… the best conditions for intensive interdisciplinary exchange and close clinical and scientific networking. Highly qualified teams of doctors, nurses and … molecular medicine, pharmacy, medicine or equivalent biomedical field of study) Strong background in translational and interdisciplinary research work … is considered a distinct advantage Desirable Experience in project management Good German language skills (Level B2) Sucessfully completed PhD thesis A …Clinical ManagementGlobal Medical Advisor Immunoassay F/M/NB
Nürtingen
Vollzeit
bioMérieux Deutschland GmbH
… within the company for specific medical areas. Provide medical input to clinical trials: investigator and site identification, protocol writing and review, … trials: investigator and site identification, protocol writing and review, study monitoring and data analysis, presentation and publication of results. … issues and environment; experience in clinical trial management and design, reimbursement environment, regulatory affairs. Ability to lead …Clinical Study Management StellenangeboteSr CRA
Home Office
Vollzeit
Thermo Fisher Scientific
… research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel … update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial … writing standards. Brings up observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to …Clinical Study
Clinical Research Associates
München
Vollzeit
Thermo Fisher Scientific
… research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel … research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and … Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits to assess protocol and …Study Management StellenangeboteAssociate Director (all genders), GLP and Early Development Quality Assurance (permanent / fulltime)
Ludwigshafen am Rhein
Vollzeit
AbbVie
… such as, toxicology, bioanalytical laboratory, analytical chemistry, clinical pathology, quality assurance and/or regulatory affairs Relevant education … principal responsibility for quality oversight of GLP and GCP regulated study activities. This means: Management of the GLP Quality Assurance Team … quality oversight of GLP and GCP regulated study activities. This means: Management of the GLP Quality Assurance Team including the GLP Audit Program at the …Management StellenangeboteHead of Quality GI KRC
Rohrdorf
Vollzeit
BI Vetmedica GmbH
… In this role, you'll be at the forefront of our Animal Health Clinical site operations, driving change, and making a tangible impact on our … for GI projects and manage facility related audits and inspections of study activities. Furthermore, you will drive the Quality of the site, manage … isn't just a job - it's a chance to reshape the landscape of our Quality Management Systems and ensure we're not just meeting, but exceeding local GxP …Clinical Study ManagementAccount Manager A & G
München
Vollzeit
RELX
… for the benefit of humanity. We serve the research, academic and clinical communities through the application of technology and analytics to … our people. With numerous wellbeing initiatives, shared parental leave, study assistance and sabbaticals, we will help you meet your immediate … and other sales enablement tools and adjust actions accordingly. Pipeline management and accuracy with Salesforce. Gather, monitor and evaluate competitive …Clinical Study ManagementMedical Education Manager
Home Office
Vollzeit
Shockwave Medical
… to lay audiences in a clear and concise manner. Ability to interpret clinical and other complex information and data and capable of teasing out relevant … & reporting. Requirements A bachelor’s degree in a related field of study. Advanced degree preferred. 4+ years of experience in a medical device … and accuracy, experience establishing processes and systems. Good project management skills. Proficient in PowerPoint. Good prioritization and organizational …Study StellenangeboteClinical Operations Lead
Home Office
Vollzeit
Alimentiv
Responsible for the clinical operations of a project within a defined regional/global level. Provides … metrics, issue escalation and corrective actions. The COL will develop study tools for site and CRA use, review visit reports, review and track … Oversee regional startup and feasibility activities. Assist in vendor Management activities as required per project. Perform review of visit reports for …Study ManagementClinical Research Associate, sponsor dedicated
Home Office
Vollzeit
ICON
The Clinical Research Associate will perform site activities for Phase I-IV studies … reports in a timely manner Knowledge of applicable SOPs, guidelines and study procedures Conduct study start-up activities related to in-house … monitoring visits, and site close-out visits. Perform investigator site management activities in adherence to all applicable regulatory guidelines and …Study ManagementMedical Scientific Liaison (all genders) - GM Multi Asset CardioRenal/Womens Health - South-East
Grenzach-Wyhlen
Vollzeit
Bayer
… Societies with regards to Bayer products Internal scientific support and Clinical Research Support: You serve as an internal scientific expert by … and formats to disseminate, clarify, and educate on scientific data, study protocols, meeting abstracts, and professional literature. This includes … You possess a solid understanding of therapeutic area products, project management, and clinical trial design and rationale Your excellent presentation and …Clinical Study StellenangeboteExpert Statistical Programming (m/f/x)
München
Vollzeit
Daiichi Sankyo Europe
… Knowledge of SAS language, procedures and options commonly used in clinical trial reporting including the Macro language, BASE SAS, SAS/STAT and … are on time and within budget. The position holder will support study lead and partner with internal and external stakeholders to optimize … selection. Reviews base-line budget and timelines. Contributes to budget management and activities across the project duration Operational Excellence …Management StellenangeboteClinical Research Associate (all levels), Oncology, FSP, home based, client dedicated
Home Office
Vollzeit
Syneos - Clinical and Corporate - Prod
Description Clinical Research Associate - home based, sponsor dedicated, flexible level based … of site relationships through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor … through all phases of the trial. Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local …Clinical StellenangeboteClinical Evidence Specialist (f/m/d)
Heidenheim an der Brenz
Vollzeit
HARTMANN
… At HARTMANN we believe in the difference you can make. Join our team as Clinical Evidence Specialist (f/m/d) DEU-Heidenheim We are seeking a highly … Devices and digital health solutions Understand clinical epidemiology and study designs to contribute to protocol development Review existing evidence and … communication and interpersonal skills Demonstrated ability in project management Fluent in English Benefits: Flexible working conditions, such as flexible …Clinical Study