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JOB DESCRIPTION :
The primary function of the Clinical Research Coordinator is to coordinate the conduct of
Clinical research protocols in the in-hospital with an emphasis on the screening, enrollment, and monitoring of patient candidates/participants.
Assist in the compilation of all trial related documents during the pre-trial period.
Follow up with clinical site team for timely completion of the EDC and to coordinate with delegated site staff to ensure that all the relevant information required in the Case Record Forms are present in the source documents.
Compile and update the Investigator Site File (ISF).
Maintain all the study related logs in ISF screening, enrollment and other communication logs, IP &/or blood samples temp logs/ IP accountability logs etc including forwarding all relevant logs to Klinera/Sponsor in a timely manner.
Manage the inventory of all non-clinical study supplies received &/or returned at site level.
Assist in scheduling subject visit as per the protocol, by regular telephonic follow-ups/ reminders as applicable.
Coordinate all lab related activities shipment of samples through the designated courier and ensure timely receipt of the lab reports.
Clinical research protocols in the in-hospital with an emphasis on the screening, enrollment, and monitoring of patient candidates/participants.
Assist in the compilation of all trial related documents during the pre-trial period.
Follow up with clinical site team for timely completion of the EDC and to coordinate with delegated site staff to ensure that all the relevant information required in the Case Record Forms are present in the source documents.
Compile and update the Investigator Site File (ISF).
Maintain all the study related logs in ISF screening, enrollment and other communication logs, IP &/or blood samples temp logs/ IP accountability logs etc including forwarding all relevant logs to Klinera/Sponsor in a timely manner.
Manage the inventory of all non-clinical study supplies received &/or returned at site level.
Assist in scheduling subject visit as per the protocol, by regular telephonic follow-ups/ reminders as applicable.
Coordinate all lab related activities shipment of samples through the designated courier and ensure timely receipt of the lab reports.
Salary:
INR 1,00,000 - 3,00,000 P.A. Best in industry
Industry:
Medical / Healthcare / Hospitals
Functional Area:
Medical, Healthcare, R&D, Pharmaceuticals, Biotechnology
Role Category:
R&D
Role:
Clinical Research Associate/Scientist
Keyskills:
* Should be good in Drug DevelopmentICH GCP guidelinesClinical trials and soft skills
Desired Candidate Profile
Education:
UG - B.Pharma - Pharmacy, MBBS - Medicine
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required, M.Pharma - Pharmacy
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
PG - Any Postgraduate - Any Specialization, Post Graduation Not Required, M.Pharma - Pharmacy
Doctorate - Any Doctorate - Any Specialization, Doctorate Not Required
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