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Wednesday, 18 May 2016

Job Description


    Job Description: 
    • Preparing case studies, medical abstract writingmedical write - ups for media publishing and Newsletter under the guidance of the Chief Scientific Officer & Technical Director. 
    • Preparing Manuscript for publishing.
    • Preparing market report, product monograph, ppt.
    • Managing, Coordinating & Maintaining Intellectual Property trademark, copyright of existing and new product.
    • Meeting the statutory body as and when required. 
    • Adhering to SOPs, regulations, good clinical and ethical practices and protocol procedures
    • Coordinating between sponsors, investigators and CRO
    • Facilitate monitoring
    • Schedule patient visits and follow-up visits
    • Investigational product storage and accountability
    • Maintenance and completion of study files
    • Coordination with Data Management and resolution of queries
    • Completion and verification of source documents
    • Monitoring and verification of essential documents (Protocol, CRF, ICF, etc)
    • Communicating with Ethics Committee for submission of study related reports
    • Maintaining subject screen logs and protocol deviation logs
    • Maintaining spreadsheet tracking updates of database of all clinical trial related activities
    • Communicate with central laboratory for logistics/shipment from investigator sites 
    • Carry out any other job-related activities as and when deemed necessary

Desired Candidate Profile

Education-
UG:B.Sc - Other Specialization, Other Specialization
PG:PG Diploma - Other
Doctorate:Doctorate Not Required
    Graduate (Pharmacy/Science/Biotech) and Diploma / Degree in Clinical Research
Company Profile:
Regenerative Medical Services Pvt. Ltd.
A leading Biotech Company.
Recruiter Name:Ms. Gauri
Contact Company:Regenerative Medical Services Pvt Ltd
Telephone:9619558176
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