...Submission Teams (CST) to ensure compliance of documentation to internal company standards and external regulatory guidelines.
Program Writer ensuring adequate medical writing resources are available for assigned...
...drug and device development firm, we guide our clients across all phases of clinical research to efficiently bring new products and therapies to market. Over the past forty years, our expert teams have helped earn m...
Your responsibilities will include:
Advise on current and future digital strategies for sensors, wearables and medical devices deployed in clinical studies that align with the needs of the cardiovascular and metabolic portfolio.
Conduct up-to-...
...is a leading company in the None industry, specializing in data research and analysis. Our team of experts delivers high-quality insights... ...industry.
Role And Responsibilities
As a ...
...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...
• Advise on current and future digital strategies for sensors, wearables and medical devices deployed in clinical studies that align with the needs of the cardiovascular and metabolic portfolio. • Conduct up-to-date and state-of-the-art advanced data...
...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...
...programming strategies, standards, specifications and programmed analysis
Support the electronic submission preparation and revi e w
Reviews key planning documents (e.g., statistical analysis plan, data p...
...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...
