Job in Drug Safety Associate at Wipro
Careers at Wipro Ltd company, Grab this career opportunity to work in Wipro Ltd. Wipro hiring for Freshers and Experienced Jobs candidates to work with the Company Wipro posting new jobs Vacancy frequently as per availability of vacant post, Here you can check eligibility criteria and qualifications, experience required for the position, and jobseeker candidates can Apply Online for Current Wipro Job Openings find more Pharma Jobs post.
About Wipro Ltd
Wipro Limited is a leading technology services and consulting company focused on building innovative solutions that address clients’ most complex digital transformation needs.We leverage our holistic portfolio of capabilities in consulting, design, engineering, operations, and emerging technologies to help clients realize their boldest ambitions and build future-ready, sustainable businesses.
Interested & eligible candidates need to apply online via the given official website/address. You will get brief information on Wipro Drug Safety Associate jobs openings like educational qualifications, selection process, eligibility criteria, and important dates given in the below article. So read this article till the end to get all the information regarding this recruitment. For more jobs visit www.tyropharma.com.
| Wipro Drug Seafty Associate Jobs Opening Details |
|---|
Job in Drug Safety Associate at Wipro
Post Name: Drug Safety Associate
Qualification: M.Pharm / B.Pharma / BAMS / BHMS / PhD./ Pharm D / BDS
1) Sound knwoledge of regulatory guidelines related to PV domain
2) Narrative Writing
3) 3) MedDRA Coding
4) Familiarity with pharmacological concepts
5) Command on verbal and written communication skills
Job Location: Pune, India
Job Description
1. Reviewing the published reports/biomedical literature to ascertain if they contain individual case reports and Non-individual case reports.
2. Applying regulatory and internal guidance to determine if the article meets the definition of a valid case report and Non- individual case reports.
3. Write accurate and concise summaries that capture the key elements from these published reports.
4. Ensure consistent coding of medical history, drugs and adverse event terms.
5. Evaluation of Serious Adverse Event to ensure accurate processing from source documents with emphasis on quality and timeliness.
6. Creating summary content in a range of formats (narrative summaries, structured database inputs, electronic formats for regulatory filing) to support the drug safety reporting and information requirements of pharma industry client.
Selection Process
- Based on Written / Personal Interview
How to Apply
- Interested candidates fulfilling the eligibility criteria can apply for this job.
- Candidates can easily apply online through the following link. You can also visit the company's official website career page for further details.
- If a job opening is scheduled Walk-in-Interview then candidates are requested to read Walk-in Date, Time & Venue carefully.
| Important Links For | |
|---|---|
