Cipla Released Job Openings On 01/10/2022.Cipla Limited is an Indian multinational pharmaceutical company, headquartered in Mumbai, India.Interested and eligible candidates required to fill application form in online with Education and personal details and submit application along with resume .Job application form link provided at the end of post. Eligibility for the Therapy Manager / Medical Represetative as follows.
Cipla Recruiting B. Pharm/B.Sc. for BABE and For clinical B. Pharma or M.Sc. Or M.B.B.S.B. V. Sc. & A.H is compulsory. M. V. Sc. (Pharmacology and Toxicology) Graduates with 02+ yrs of relevant experience for Team Member – Clinical/Pre-Clinical/BABE Position.Complete Details for the Team Member – Clinical/Pre-Clinical/BABE as follows.
Important Details :
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application:01/10/2022
- 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 : Call/ Email Resume : Sun Pharma Job Vacancy Salary ₹ 15,00,000 – 18,00,000 P.A.
Freshers & experience B.sc,M.sc,B.pharm,M.pharm,ITI,Diploma,D.Pharm,B.tech,M.tech,Any Graduate Jobs In QC, QA, Production, Engineering, R&D, Micro, Store ,Sales,Medical Coding All Departments In Multiple Locations
Job Description/Skills Required
Execute, monitor, report and interpret preclinical, clinical and BABE studies at CROs to support various regulatory submissions within targeted timelines, budgets, quality and regulatory guidelines; identify health hazard and assess risks associated with pharmaceuticals/ chemicals/ intermediates/ impurities, etc. by toxicological review and derivation (Only for preclinical)AccountabilitiesI. Gather preclinical/ clinical/ BABE study outline data by understanding the specific regulatory requirements and project constraints to ensure successful conduct of studies/trials cost effectively and within timelinesII. Check CROs for conducting preclinical/ clinical/ bio equivalence studies by site feasibility/ selection visits or evaluation for ensuring adequate facility, skill and experience for conducting the studies as per requirementsIII. Liaise with CROs and internal team to enable preparation, review, and finalization of study protocol as per the defined strategy to ensure that protocol is approved by all relevant stakeholders, Ethics Committee, and/or Regulatory authorities within targeted timelinesIV. Ensure procurement and dispatch of Innovator samples/ RLD and availability of test formulation along with relevant documents (like COA, GMP statements, batch size information etc.) before study initiationV. Monitor and/or audit ongoing studies at CROs to ensure satisfactory conduct as per requirements (guidelines, regulatory, study specific, etc.) and project timelinesVI. Act as the project coordinator for the entire study by liaising with internal team members, cross-functional teams, CROs and Project Managers to align all stakeholders and successfully conduct the BE study