...allows for the questioning and challenging of others in a respectful and constructive manner.
Qualifications & Experience
~ Fresh P hD with 3+ years experience or MS with 5 + years experience in statist...
...Transparency submission documents are delivered in accordance with timelines, high quality, operational and technical procedures.
May attend Transparency Submission planning meetings with cross-functional team me...
...maintain sound working relationships and effective communication within the Clinical Trial Team and Biostatistics & Pharmacometrics team.
h. Oversee all Biostatistics resources and deliverables for assigned trial...
...The Document Coordinator is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical documentation.
The Document Coordinator will interact with cli...
...The Senior Manager of Biostatistics is a member of cross-functional development teams and contributes to trial design, protocol development, analysis planning, interpretation of results, and prep...
...Responsible for Clinical execution and management of all aspects of assigned clinical studies (interventional and non-interventional, from... ...and operational procedures. Might be required ...
...for CT under the EU Regulation.
Position Responsibilities
Manage the signing of clinical trial documentation such as powers of attorney, expected to be able to coordinate many signing at the same time.
Prov...
...About The Role
Senior Clinical Data Scientist
Location – Hyderabad Hybrid
About the Role: Provide timely and professional ongoing management of Data Management deliverables and of clinical trial data with r...
...Statistical programmer will responsible for statistical programing for clinical trial studies. Programmer will develop and validate SAS programs for datasets, and outputs (TLFs).Looking for well experienced candidat...
