Torrent Pharmaceuticals Limited Walk In Interview 2023.Torrent Pharmaceuticals Limited Notification full details below.Interested and eligible candidates can attend interview on scheduled time and venue.The flagship company of the Torrent Group, Torrent Pharmaceuticals Limited is a major player in the Indian pharmaceuticals sector with the vision of becoming a global entity. Torrent Pharma enjoys dominance in the niche therapeutic areas like, cardiovascular and central nervous system, gastro-intestinal, pain management and oral anti-diabetic segments.
Vacancy details:
- Department: CLINICAL RESEARCH EXECUTIVE (BA/BE STUDIES)/CLINICAL RESEARCH ASSOCIATE
- Qualification: M. Pharm / M.Sc (Clinical Research)/B.Pharma in Any Specialization
- Experienced: 2-7 Yrs of Relevant Experience
Job Description: Greeting from Torrent Pharmaceuticals Limited !!!!
Important Details :
- Location: Ahmedabad
- Post of date:30/08/2023
- Selection Process: The selection will be on the basis of Interview.
- Mode of Interview: Face to Face interview
- Interview Rounds of Interview: HR
Role & responsibilities
Feasibility assessment/ new product evaluation
Literature review and BA/BE study designing
BE Study Monitoring
Preparation of documents for regulatory submission (i.e BENOC, Import license application etc.)
Establishment and maintenance of study documents
Document preparation for dossier submission (i.e clinical overview, non-clinical overview, summery tables etc.)
Review of BE study documents i.e protocol, reports, ICF etc.
Preparation/review of medical write up
Coordination for serious adverse event reporting and safety update to Regulatory agency
Preferred candidate profile
M.Pharm (Pharmacology) with 02-05 Years of Relevant Experience
Interested Candidates are requested to share their CVs on vilshashah@torrentpharma.com
CLINICAL RESEARCH ASSOCIATE
Role & responsibilities
Study start-up: Site identification, evaluation, selection, EC submission dossier preparation, Site contract / CTA
Site management for clinical trial : Site initiation & liaisoning, Site staff training, re-training, Oversee sites on patient recruitment, patient retention etc., Site recruitment issue/trouble-shooting, Study monitoring, ensure data quality, Support site audits ,Site close out Management of clinical trial supplies
Vendor management
Project management : Tracking timelines & budget , Site & vendor invoice payments
coordinate with cross functional teams
Preferred candidate profile
M. Pharm / M.Sc (Clinical Research) with 02-05 Yrs of Relevant Experience
Interested candidates may share their CVs on vilshashah@torrentpharma.com
