- Job Description:
- Preparing case studies, medical abstract writing, medical 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-
- Graduate (Pharmacy/Science/Biotech) and Diploma / Degree in Clinical Research
Company Profile:
Recruiter Name:Ms. Gauri
Contact Company:Regenerative Medical Services Pvt Ltd
Telephone:9619558176
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