Clinical Research Coordinator (CRC) position at New Delhi based CRO.
Post : Clinical Research Coordinator (CRC)
No of Posts: 3
Job Description:
• Participate in the study specific training meeting.
• Be a point of contact between investigator, site staff and Sponsor/CRO.
• Screening of eligible patients according to inclusion/exclusion criteria.
• Assist in the administration of Informed Consent Document.
• Undertake randomization and blinding (where applicable).
• Scheduling of patient visits and protocol specific investigations.
• Follow protocol schedule of events and ensure compliance to the study protocol.
• Maintain essential clinical trial documents such as master file, source document, CRF, ethics approval/communication etc.
• Procurement, storage, dispensing and return of investigational product along with 100% accountability.
• Data entry in paper CRF or EDC followed by query resolution.
• Ensure access control for the study documents and investigational product throughout the duration of a clinical study.
• Ensure proper storage and archival of study documents after the completion of study.
• Operate to the highest level of ethical and moral standards
Candidate Profile
• B. Pharma, M. Pharma with clinical research training and certification along with a minimum of 6 months CRC experience
• B.Sc., M.Sc. with clinical research training and certification along with a minimum of 12 months CRC experience
Additional Information:
Experience : 1 Years
Qualification : M.Pharm, M.Sc, B.Pharm, M.Sc
Location : New Delhi
Industry Type : Clinical research
Functional Area : CRC
CTC: Rs. 2.5 lac per annum
End Date : 30th January, 2018
Send your Resume at : info@catalystclinicalservices.com
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