...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...
...we can help you build the career you want - developing your skills, working on challenging problems, to ultimately develop clinical therapies that matter
Provide project and technical support in the preparation, ...
...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...
...submission activities and documents, meetings with and responses to Health Authorities and other drug development activities, as required
c. Contribute to interactions with external review boards/ethics committee...
...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...
