...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...
Clinical Research Associate II / Senior CRA - Cardiology
The Clinical Research Associate is the person in Trial Coordination and Site... ...strategic resourcing and FSP services to the biopharmaceu...
• Deliver timely consistent, accurate and reproducible coding of clinical trial data using industry standard
coding dictionaries (MedDRA, WhoDrug) in line with global and therapeutic area guidelines.
• In collaboration with Global Data Manager, ...
...trial activities for our medical device portfolio, ensuring compliance with international regulatory standards for markets including the U.S. and Japan. The role requires extensive experience in clinical trial manag...
...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...
...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
The Senior Study Leader is responsible for the execution and delivery of the Global Clinical Operations (GCO), clinical studies in accordance with the Operational Execution Plan (OEP) and clinical study protocol.
You will lead t...
Clinical Research Associate II / Senior CRA CardiologyThe Clinical Research Associate is the person in Trial Coordination and Site Management that serves as primary contact point between the sponsor and the investigational site. This position is assi...
...Manager, Clinical Trial Transparency is to drive the delivery of activities related to data disclosure in GSK RD in the respective therapy area (Oncology, Specialty, Vaccines)
The role is accountable to ensure c...
...close out activities including but not limited to site close out, final drug accountability and audit/inspection readiness of Trial Master File documentation
• Promotes operational excellence and contributes to the ...
Hyderabad
Novartis India
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