Biocon Biologics Released Job Openings On 17/02/2022.Biocon Biologics is a globally recognized, innovation-led organization that is enabling access to high quality, advanced therapies for diseases that are chronic, where medical needs are largely unmet and treatment costs are high.
Vacancy Details:
Biocon Biologics Recruiting M Pharm, M.Sc Candidates with 06 Years of Experience for Clinical Operations Lead Position.Complete Details for the Clinical Operations Lead as follows.
Important Details :
- Location : Bengaluru
- No of Vacancies:Not Disclosed by Recruiter
- Details of Salary: Not Disclosed by Recruiter
- Opening date for online Application: 17/02/2022
- 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 : Submit Resume : FRESHER And Experienced Openings At Bharat Serums and VaccinesÂ
Job Description/Skills Required
1. Identification and selection of appropriate CROs thorough review of proposals and onsite selection visits and participate in CRO biding process
2. Identification and selection of appropriate third party study vendors
3. Drive the selection of CROs, vendors in the conduct of outsourced multinational clinical trials
4. Develop budget and timelines as per the CDP from the inception stage of the project
5. Manage program budgets and track overall quality on multiple clinical trials
6. Give strategic inputs to improve quality and efficiencies through quality management plans.
7. Driving clinical trials independently across various geographies
8. Oversee performance of CROs, third-party vendors, including co-monitoring, to ensure compliance with the study protocol and in accordance with the scope of work; identify areas of concern and escalate to CRO or seniors as appropriate
9. Prepare a robust CRO oversight plan and escalation path for the conduct of the trial
10. Ensure studies are carried out according to the study protocol, SOPs, and ICH/GCP regulations, and study-specific manuals and procedures
11. Track and report on the progress of study including site activation, patient enrollment, monitoring visits, etc
12. Monitor progress of trial and timelines as per the milestones and implement appropriate action plans in case of delays
13. Negotiate and manage the budget and payments for investigative sites, as applicable
14. Co-ordinate closely with the clinical development team and other cross-functional representatives, including Biostatistics, Pharmacovigilance, Regulatory/QA, formulation team, program management, etc. to ensure successful completion of all project deliverables within the required time frame and budget
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