Dr. Reddys Laboratories Released Job Openings On 25/07/2022. Dr. Reddy€™s Laboratories Ltd. (NYSE: RDY) is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Dr. Reddys Laboratories Recruitment 2022 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Dr. Reddys Laboratories Recruiting Any Graduate with 08-13+ Years of Experience for Project Manager For Clinical Operations Position.Complete Details for the Project Manager For Clinical Operations as follows.
Important Details :
- Location :Hyderabad/Secunderabad, Bangalore/Bengaluru, Mumbai (All Areas)
- No of Vacancies:NA
- Details of Salary: ₹ 18,00,000 – 30,00,000 P.A.
- Opening date for online Application:25/07/2022
- Mode of application :Online
- How To Apply: At the End of the Article We Have Provided Source Link,Please Go through that and Follow Necessary Steps
Related Job: QC,QA,R&D,Maintenance,Production Dept Walk In On 26th & 27th July 2022 At Kekule Pharma
Job Description/Skills Required
- Identify different CRO/Vendors and roll-out RFI and RFP; Facilitate CRO/Vendor finalization
Assess RFI/RFP information and shortlist CRO for further comparisions, discussions with HOD and senior leaders; Paricipate in vendor selection visits as Clinical Operations SME - Contribute in developing Clinical trial execution startgeies/plan and also execute the clinical trials as per Clinical development startegies.
Perform IP/RMP forecast for the entire project and monitor the inventory at depot and at sites to ensure adequate drug is available.
Define various recruitment initiatives in coordination with CRO/vendor
Contribute in review and finalization of various clinical trial documents/plans like Study Monitoring Plan, project management/communication plan, RACI etc.
Review various project specific Work orders, Change Orders, study invoices etc.
Ensure compliance of sponsor oversight plan by reviewing monitoring reports, CRF data, monthly listings/reports, perform onsite visits etc.
Establish and maintain relationship with clinical trial sites - Ensure all aspects of study site management i.e. recruitment of qualified investigators, site initiations, conduct investigator meetings, ensure enrollment criteria are met and other aspects of the study management as appropriate.
- Build and maintain good working relationship with CRO/Vendor; Prepare and conduct F2F meetings with CRO on need basis
Click here for Official notification and Apply
