Job Description

Role expectations:The primary responsibilities and accountabilities of our Senior Medical Writer (designation flexible would depend on candidature) are:- Responsible for writing and reviewing study documents such as Protocol, Synopsis, Informed Consent, Data Collection Documents and Study Report, etc.- Responsible for developing scientific communication such as abstract, poster, manuscript, etc.- Responsible for performing quality control for medical writing deliverables- Responsible for interpreting statistical results and for soliciting statistician input for developing study reports, abstracts, manuscripts, and other documents as required- Participating in the improvement of the quality assurance system- Responsible for participating in bid-defense presentations representing medical writing activities for real-world studies- Manage publications based on Healthplix RWE end to end. Work on clinical data extracted from Healthplix and provide advice for the publication requirements of the clientKey skills and Background :- Advanced degree in a scientific discipline, preferably PhD, PharmD or MD- 1-3 years of professional experience in Medical Writing at a pharmaceutical, biotechnology, CRO or other healthcare setting- Proven knowledge of ICH/GCP and GPP guidelines or other meaningful guidelines or industry-standard- Outstanding written and verbal interpersonal skills- Good computer literacy- Ability to work effectively and cooperatively with cross-functional teams- Good to have a background/ work experience pertaining to real-world studies. (ref:biojoby.com)

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