... clinical trial principles) and good knowledge of regulatory submissions and requirements Ability to ... experience preferably in processing clinical trial data in the biotechnology, pharmaceutical or health ...

... , techniques and clinical trial principles) and good knowledge of regulatory submissions and requirements ... + years of programming experience preferably in processing clinical trial data in the biotechnology ...

... The Senior Clinical Data Manager will serve as the DM study lead and point of contact for clinical ... aspects of DM activities across all stages of the trial from study start-up through archiving to achieve ...

... statistical concepts, techniques, and clinical trial principles). Knowledge of regulatory submissions and ... processing clinical trial data in the biotechnology, pharmaceutical or health related industry ...

... , techniques, and clinical trial principles). Knowledge of regulatory submissions and requirements is a plus ... support ongoing clinical studies and requests for study report, regulatory submission, and ad hoc/post hoc ...

... We are seeking a highly motivated Senior Manager, RBQM Data Analys t will be a subject matter expert for Central Monitoring RBQM systems. The Senior Manager, RBQM Data Analyst is ...

... The Digital Health Technologies (DHT) Manager is accountable for electronic COA (eCOA) in individual clinical research studies from study design to close out in collaboration with the study team. In ...

... processing clinical trial data in the biotechnology, pharmaceutical or health related industry. SAS ... ongoing clinical studies requests for statistical and non-statistical analyses. Meets statistical ad hoc ...

... Act as the primary clinical/scientific resource to HCPs in the territory for information pertaining to ... development and management of company sponsored clinical trials including. Establishing scientific ...