Clinical Investigator Jobs in Bangalore
Biocon Biologics - Bengaluru, Karnataka, India
-issues report. Attends regular meetings with CRO and/or other vendors. Supports and oversees activities of study conduct e.g. site selection, interaction with investigators and other service providers
from: linkedin.com - 5 days ago
MS CLINICAL RESEARCH - Bengaluru, Karnataka, India
requirements. Build and maintain strong relationships with investigative sites, investigators, and study coordinators. Clinical Trial Monitoring : Perform routine monitoring visits to assess site performance
from: linkedin.com - 27 days ago
Novo Nordisk - Bangalore, Karn, IN
. This includes but is not limited to, the preparation of Protocols, Clinical Trial Reports (CTRs), Non-interventional study reports (NSRs), Meeting packages and briefing books, Investigator Brochure (IB
from: Novo Nordisk - 9 days ago
Novo Nordisk - Bangalore, Karn, IN
) from clinical trials, investigator sponsored trials, named patient supplies and third-party trials, ensure appropriate medical interpretation and evaluation of adverse events reported from world-wide sources
from: Novo Nordisk (+1 source) - 13 days ago
Quanticate - Bengaluru, KA
. Responsibilities: Produce well-written, high-quality, timely Medical Writing documents (like Clinical Study Reports, Protocols and amendments, Investigator's Brochure [IB] and IB updates, etc) Review (including peer
from: workable.com - More than 30 days ago
Novo Nordisk - Bangalore, Karn, IN
to the preparation of Protocols, Clinical Trial Reports (CTRs), Non-interventional study reports (NSRs), Layperson Summary (LPS), Investigator Brochure (IB), Regulatory response documents (Q&A), Clinical summaries
from: Novo Nordisk - More than 30 days ago
Novo Nordisk - Bangalore, Karn, IN
) from clinical trials, investigator sponsored trials, named patient supplies and third-party trials, ensure appropriate medical interpretation and evaluation of adverse events reported from world-wide sources
from: Novo Nordisk - 16 days ago
Merck - Bengaluru
As a Senior Specialist Medical writer , you will support the Global Medical Writing Team to deliver its portfolio effectively and efficiently Independently author clinical and regulatory documents Not disclosed INR
from: naukri.com - 8 days ago
Fortrea - Bengaluru / Bangalore, India
as appropriate to finalize site contract language. ♦ May liaise with Investigator Grant team, Clinical Operations team, and sites to develop, modify, and monitor site budgets and payment terms. ♦ May obtain Not Mentioned
from: Monsterindia.com - More than 30 days ago
PSI Cro - Bengaluru / Bangalore, India
)/Independent Ethics Committees (IECs) on project-specific medical and safety-related questions Collaborate with internal departments in the preparation of clinical development plans, protocols, investigator Not Mentioned
from: Monsterindia.com - 29 days ago
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