WhatsApp D. Pharma Group
Join Now
Telegram D. Pharma Group
Join Now
Telegram Group Latest Pharma Jobs
Join Now
Telegram B. Pharma Group
Join Now
Telegram Medicine Update Group
Join Now
WhatsApp B. Pharma/ GPAT Channel
Join Now
The Medical Writer is expected to work under guidance of a mentor or independently, facilitating delivery of the written assignments through proactive coordination of stakeholders to build content. The writer understands trial designs and interpretation of statistically analysed clinical research data. The writer should be able to meet the quality standards of the global organization. The Medical Writer is responsible for the final deliverable and is expected to work in complex matrix organizations
Key Responsibilities:
- Completes assignments under guidance of a mentor or independently (this may include sections, or whole documents).
- Authors clinical regulatory documents following defined templates.
- Independently builds and expands capabilities to work on increasingly complex assignments.
- Understands the importance of consistency and quality level for all documents.
- Establishes network of communication and continuously builds these relationships with stakeholders to facilitate efficient execution of assignment.
- Participates in document planning and review meetings.
- Proactively raises and discusses concerns/ issues in an open and timely manner within the global Medical Writing Team
- Promotes high scientific and medical writing standards by pointing out obvious flaws and proposing alternatives.
- Interprets and communicates clinical data clearly and succinctly and at an appropriate level for the audience.
Required:
- MSc or MPharm – Lifesciences
- Up to 2 years writing experience in the pharmaceutical industry is a plus
- Demonstrates knowledge of scientific methodology in the design, conduct and description of clinical research.
- Demonstrates understanding of how to interpret, describe and document clinical data.
- Ability to understand importance of International Committee for Harmonisation (ICH) / Good Clinical Practice (GCP).
- Possesses good working knowledge of statistical principles used in clinical research
- Shows good attention to detail
- Possesses necessary computer skills and general computer literacy.
- Excellent English language skills (verbal and written)
Site Name:Â Bengaluru Luxor North Tower
Department: Medical and Clinical
