DDReg Pharma Released Job Openings On 25/03/2022.DDReg is a global regulatory advisory company for pharmaceutical countries with operations in many cities of India and world. Founded by Ms. Neeti Pant, an alumni of IIT BHU in 12 overs DDReg has been a trailblazer in its field and works with almost all the major pharmaceutical companies in India and abroad.Eligibility Criteria / Educational Qualification, Official Notification, Apply Online Form Link & Other Relevant Details for DDReg Pharma Recruitment 2022 are provided below.
Vacancy Details:
DDReg Pharma Hiring B.Sc, B.Pharma With 02-07 year(s) of experience for Associates/Sr. Associates Pharmacovigilance Profile Position.Complete Details for the Associates/Sr. Associates Pharmacovigilance Profile as follows.
Important Details :
- Location : Hyderabad/Secunderabad
- No of Vacancies:NA
- Details of Salary:NA
- Opening date for online Application: 25/03/2022
- Mode of application :Online
- How To Apply: Interested Candidates Share resume at hetal.y@ddreg.in
Job Description/Skills Required
- Taking care of rapid and timely processing of new and follow-up reports of adverse events and side effects (Adverse Events, or AEs), as well as Serious Adverse Events (SAEs) and Suspected Unexpected Serious Adverse Reactions (SUSARs) which are unexpected SAEs with (possible) causality to the (study) drug, both from spontaneous reports (out of the market) and out of clinical drug research;
- Processing all the AEs, SAEs and SUSARs in the Global Safety Database according to the applicable Company Policies and Standard Operating Procedures (SOP’s), and as required by the Competent Authority for reporting adverse events;
- Contacting reporters of the adverse events and side effects to obtain complete information for analysis;
- Ensuring that product complaints are assessed according to AE, SAE, and SUSAR criteria and forwarding eventual (S)AE’s and SUSAR’s to the head office;
- Contributing to keeping local processes, procedures, and systems up to date for recording and processing of side effects;
- Assisting with the preparation of the audit/inspection and participating in the audit/inspection when appropriate;
- Perform Literature Search
- Review Literature-based Case Studies.
- Carry out MedDRA/WHODD coding
- Carry out the reconciliation of cases on a periodic basis
- Archive the documents on the server
- Assist ICSR Team Lead on Day to Day ICSR Management & Reporting
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