...the impact you could have.
Job Purpose:
The SSO Clinical Project Manager (CPM) is accountable for the day-to-day planning, executing... ...and diverse teams representative of the patien...
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...
...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...
1) Act as DRLs direct contact with assigned sites, assess and ensure overall integrity of study
2) Implementation and adherence to study protocol at clinical investigational sites, and resolve site issues. Escalate issues that were unresolved to ...
...Location: Delhi/Mumbai/Hyderabad
Business Unit: CMR (Clinical, Medical, Regulatory & Pharmacovigilance)
Are you passionate about what you are doing? Do you want to build excellence within processes in the ...
...clinical trial related safety exchange agreements in line with regulatory requirements and internal company SOPs.
Make presentation w.r.t safety reporting for IM or site initiation visit (SIV) as required.
...
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...
...Job Description :
1) Should be a medical doctor - preferably with MD in Pharmacology
2) 4+ years- experience in handling Phase 2/Phase 3 clinical trials in India
3) Manage the CRO team for all clinical ...
...You will be expected to develop and review complex edit checks, patient profile listings, reports, preprocessing checks & map datasets for validation based on study requirements using different tools/techs such as Cognos / SAS, ...
Bangalore
Inspiration Manpower Consultancy Private Limited
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