Intas Released Job Openings On 05/08/2022.Intas Experience spanning three decades in healthcare, with a wide range of formulations to meet the needs of ailing humanity, Intas Pharmaceuticals headquartered at Ahmedabad (India), is now a force to reckon with, in the global pharma horizon. With expertise in a range of formulations, from tablets to injectables to newer drug delivery systems, Intas is currently ranked 17th among the Indian Pharma majors..Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for Intas Recruitment 2021 are provided below. Interested and eligible candidates can submit application along with resume.
Vacancy Details:
Intas Recruiting Medical-MS/MD candidates with 00-01 Years Experience for Medical Writer Position.Complete Details for the Medical Writer as follows.
Important Details :
- Location :Ahmedabad
- No of Vacancies: NA
- Details of Salary:NA
- Opening date for online Application: 05/08/2022
- 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: Virtual (Zoom) Interview : 700 Urgent Openings At Pacific BPO Pvt Ltd ( Call/Watsapp/Email Resume )
Job Description/Skills Required
Handle clinical development and medical affairs efficiently with following responsibilities
- Clinical and Non-Clinical development for different markets
- Support Device development
- Medical writing
- Regulatory support
- Support PVG activity
- Work in collaboration with stake holders and implement assigned activity
Responsibilities
- Responsible for the following activities Clinical and non-clinical development for Global, RoW and National market
- Clinical development plan, Scientific advices
- Preparation of synopsis for expansion to protocol by CRO
- Conduct of the trial
- Medical writing
- Support product evaluation
- Regulatory support activities
- Regulatory query handling for clinical and PVG
- Prepare or review PI
- Prepare regulatory submission dossier for clinical and animal studies Device development support
- Support HF study conduct Support PVG activity
- Identifying ADR from complaints
- Preparation or review of individual cases, PSUR, RMP
- Support Biotech and Plasma fraction related PVG work
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