Clinical Research Coordinator I
Hamburg
Vollzeit
Velocity Clinical Research, Inc.
Overview: Velocity Clinical Research is an owned and integrated research site organization, providing … Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. Responsibilities: Role & … with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, …Study Management StellenangeboteManager Study Start-up
Homeoffice
Vollzeit
Parexel
… Milan, Milano, Italy; Paris, Paris, France Job ID R0000016096 Category Clinical Trials ABOUT THIS ROLE The Manager, Study Start Up at Parexel plays a … Job ID R0000016096 Category Clinical Trials ABOUT THIS ROLE The Manager, Study Start Up at Parexel plays a pivotal role in Site Start-Up activities and … Start-Up for two or more clinical studies. This position includes direct management of staff within the Study Start-Up team. If you’re a SSU professional with …Clinical Management StellenangeboteClinical and Research Operations Manager
Sachsen-Anhalt
Vollzeit
Boston Medical Center
… Review Board protocols; monitor study implementation, including clinical implementation of the economic interventions we are studying; assist with … of managing the grant-funded research projects include working with the study team to develop study protocols, assessment instruments, and Institutional … goal or scientific objective. Duties include the following: Project Management Coordinates and facilitates the research project Management life cycle, …Clinical Study Stellenangebote
Specialist* Patient Operations Logistics
Mainz
Vollzeit
BioNTech AG
… future in many people's lives. Primary responsibilities include: Execute Clinical Trial Supply Management Patient Operations activities in global Phase … quality management experience Proven track record of distribution of study drugs (set up and management) in global clinical trials up to Phase III … lives. Primary responsibilities include: Execute Clinical Trial Supply Management Patient Operations activities in global Phase I-III Demonstration and …Study ManagementClinical Research Coordinator I
Wiesbaden
Vollzeit
Velocity Clinical Research, Inc.
Overview: Velocity Clinical Research is an owned and integrated research site organization, providing … Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocity’s SOPs. Responsibilities: Role & … with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, …Study ManagementDirector, Pharmacometrics
Berlin
Vollzeit
Certara
… experts enable our clients to have: Informed decision-making & reduced clinical trial burden Higher R&D productivity Improved patient outcomes & increased … analyses, dataset creation, disease modeling, trial simulation, optimal study designs, strategic decision analyses, economic modeling). Experience in … with various elements of clinical development and trial design and management and filings preferred. …Clinical StellenangeboteMedical Writer (Senior & Principal) – United States
Schwabenheim
Vollzeit
Merck Sharp & Dohme
… talent for future openings for Senior and Principal Medical Writers. Our Clinical Research and Pharmacovigilance team push the boundaries of global … teams. Demonstrates competence in writing, editing, and reviewing clinical study reports, investigator brochures, registration dossier modules, and other … problems associated with medical writing scope of work, seeks advice from management and others as needed, and exercises negotiation and communication skills …Clinical StellenangeboteAssociate Clinical Operations Manager (Regulatory) (m/f/d)
München
Vollzeit
MSD
Our Clinical Research and Pharmacovigilance team push the boundaries of global … and tracks clinical research-related payments. Payment reconciliation at study close- out. Oversees FCPA, DPS/OFAC, and maintenance of financial systems. … with oversight from Sr.COM or Manager. Ability to proactively develop risk management and mitigation plans in the country and resolve issues locally. ICH/GCP …Study StellenangeboteMedical Writer/Scientific Advisor (m/w/d)
Neu Isenburg
Vollzeit
GBG Forschungs GmbH
… und Aufbereitung von klinischen und translationalen Daten Erstellung von Clinical Study Reports in enger Zusammenarbeit mit den Abteilungen Statistik und … von klinischen und translationalen Daten Erstellung von Clinical Study Reports in enger Zusammenarbeit mit den Abteilungen Statistik und … Du bist sicher im Umgang mit MS Office-Anwendungen, Software zum Management von Literaturreferenzen sowie Grafiktools Du kannst idealerweise …Clinical Study Management StellenangeboteScientist Lab Morrison (m/f/x)
Jena
Vollzeit
Leibniz Institute for Age Research
… perform this work within our established project framework following human clinical trial and reporting standards (e.g. blinding, randomization, study … clinical trial and reporting standards (e.g. blinding, randomization, study preregistration). The current position prioritizes technical skills and … and/or Replacement Experience in Project Design and Management, Quality Management Experience in standards of (pre)clinical and reproducible science We …Clinical Study ManagementStudy 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 you’ll be helping shape an industry. The Role: As a member of the Study Start Up Team, you will play an integral role in making sure that … Trial operations and meeting regulatory guidelines Proficient project management skills. Benefits of Working in ICON: Our success depends on the quality of …Clinical Management StellenangeboteData Manager (Clinical Trials)
München
Vollzeit
Medpace, Inc.
… we are currently seeking a full-time, office-based in Munich or home-based Clinical Data Manager to join our Data Management team. This position will work in … and edit checks for the electronic data capture system used for each study; Coordinate overall Data Management by serving as primary contact for the … in Munich or home-based Clinical Data Manager to join our Data Management team. This position will work in a team to accomplish tasks and projects …Management StellenangeboteProject Management Associate (PMA)
Mannheim
Vollzeit
SCOPE International
The organization of international clinical trials requires the development of complex cross-cultural teams across … of project specific procedures Assistance with set-up and maintenance of study specific documentation (trial master file) and tracking tools Quality … setting, coupled with excellent career development prospects and a management culture that is based on an open dialogue. SCOPE International is an …Clinical ManagementResearch Assistant II, Pediatrics Research
Sachsen-Anhalt
Vollzeit
Boston Medical Center
… Makes independent judgements of suitability of potential participants for clinical trials. Conducts the enrollment of study participants, including … assistants. JOB RESPONSIBILITIES: Recruits subjects to participate in the study by using approved methodologies, such as, reaching to healthcare providers … PI and with the oversight of a child psychologist. Data Collection/Data Management Prepares and maintains Institutional Review Board (IRB) approvals and …Clinical Study Management