Position : Regulatory Medical writing & Publications writing.
- SIRO Clinpharm Pvt. Ltd.
http://www.siroclinpharm.com Please send resumes with working contact numbers and expected CTC to Rajesh.Pandey@Siroclinpharm.com
Job Profile:
- Development & Review of Medical Writing documents like Clinical Study reports, Protocols, Safety Narratives, Sub analysis reports, Investigators brochures, Manuscripts, posters, abstracts across different therapeutic areas.
- Performing quality check and/or review of above documents.
- Communicating with the sponsor, Planning & coordination with the other contributors (clinical and regulatory experts, biostatisticians as well as external contacts) to the documents.
Education & Experience:
- Graduates or Post graduates in medicine, life sciences, pharmaceutical sciences with (MD, MBBS, BAMS, BHMS,BDS or MSc/ M Pharm with PhD) with prior Medical writing experience.
- Thorough knowledge of ICH –GCP & regulatory guidelines.
Skills needed
- Good oral and written communication skills (in English language)
- Good Logical & analytical skills with ability to read, analyze, and interpret the clinical data.
- Ability to multitask & prioritize the tasks as per the timelines.
- Good time management skill s& ability to work under time pressure
- Proficiency in computers especially word & excel.
To know more about the company visit http://www.milliman.com
Company
SIRO Clinpharm Pvt. Ltd.
DIL Premises, Ground Floor
Swami Vivekanand Road,
Near Tatwagyan Vidyapeeth,
Ghodbunder Road, Thane (W) 400610
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