Siro Clinpharm Recruiting For Regulatory Writer .Siro Clinpharm is a drug development solutions provider to the global healthcare industry. Our subject expertise gives us an edge in clinical trial management, clinical data management, medical writing, biostatistics & statistical programming & pharmacovigilance. In 1996 Dr.Gautam Daftary founded SIRO in Mumbai, India. In 2001 company started providing its services in Data Management. Bio statistics and a Medical Writing.The 1st breakthrough was made in 2007 when SIRO was awarded the Frost & Sullivan ‘Partner of Choice’ award for clinical trials in India. SIRO won the title ‘Clinical Research Organization of the Year’ by Frost and Sullivan for the 2nd time in a row for their India Healthcare award in 2012 And also received the Life Science Leader award for capabilities in Regulatory, Productivity, Reliability and Accessibility. It also received the prestigious D&B award in 2019.
Eligibility and other details :
- Post Name: Regulatory Writer
- Qualification: MBBS,BAMS,BHMS with 05-10 Years of Experience
- Salary: Not Disclosed
- No Vacancies: 01
- Selection Process : Based on Resume Received,will shortlist.
- – Author CSRs, IB Updates, Protocols, and Narratives – Perform robust scientific review of CSRs, IB Updates, Protocols. – Independent QC of CSRs, IB, Protocols, eCTD and non-eCTD documents – Mentoring and Training for Junior MWs would also be an added advantage – Excellent communication skills (verbal and written) with a good command over English language. – Should have worked with MNC Pharmas from US, Europe, or Japan (working with Indian Pharmas not preferred )