CRC - Berlin
... soon as possible CRC OR clinical research coordinator OR clinical study coordinator OR clinical trial coordinator OR clinical research assistant OR clinical trial assistant OR study coordinator OR trial coordinator OR ...
... soon as possible CRC OR clinical research coordinator OR clinical study coordinator OR clinical trial coordinator OR clinical research assistant OR clinical trial assistant OR study coordinator OR trial coordinator OR ...
... staff, physicians, IRB, review committees, clinical research finance team, and auditors.Act as a liaison with sponsors during study start-up activities and participate ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... monitoring requirements. Monitors activities at clinical study sites to assure adherence to GCP, ICH, SOPs, and study protocols. Tracks and supervises collection of ongoing study data for purpose of regular ...
... . Preferrable administrative support experience in clinical research, e.g. as Clinical Trials Assistant, Project Assistant, inhouseCRA, Study Start-Up Assistant. Knowledge of applicable clinical research regulatory requirements, i.e., ...
... ambition to support future state clinical trial executionLead and support all study start up activities leading, site ... and advancement of the clinical organization.Bachelor’s degree in science or related area of study Preferred• Advanced degree (E.g., ...
... coordination of assigned clinical trials throughout the trial lifecycle.Collaborate with investigators and more senior study team members by participating in ... staff) along with clinical trial sponsors, auditors, and study monitors. S he performs all ...
... focus areas include developing a study design that answers the relevant questions of the clinical trial and optimally uses existing ...
... join the team as Experienced Clinical Trials Assistant (m w d) in full- ... . Assist with periodic review of study files for completeness. Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of ...