... specific leads on EMEA regional clinical trial assignments. Identify, establish and maintain collaborative scientific relationships with key investigators, institutions, groups and consortia to ...
... a Freelance Project Manager for Clinical Supply Systems to join one ... of experience. Prior experience in clinical drug development or GMP GCP ... full-service CRO specializing in clinical development and functional solutions for ...
... the Trial Master File and Investigator Site File. Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation ...
... the Trial Master File and Investigator Site File. Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation ...
... the Trial Master File and Investigator Site File. Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation ...
... for overall coordination of assigned clinical trials throughout the trial lifecycle, providing clinical and administrative nursing support to CRC and CRN positions.Collaborate with investigators and more senior study team ...
... the Trial Master File and Investigator Site File. Assists the Project Manager (PM) and Clinical Team Leader (CTL) with generation ...
... for overall coordination of assigned clinical trials throughout the trial lifecycle.Collaborate with investigators and more senior study team ...
... join the team as Experienced Clinical Trials Assistant (m w d) ... preparation, handling and distribution of Clinical Trial Supplies and maintenance of ... a leading global provider of clinical research services, commercial insights and ...
... health authority inspections of sponsor, investigator site(s), and or CRO(s). Ability to represent the company in audits, coordinating responses with legal, clinical development, and outside vendors where ...