inVentiv Health Clinical, a leader in drug development services, has a global infrastructure, therapeutic expertise, and commitment to quality that is unmatched in the industry. For pharmaceutical, biotechnology, generic drug, and medical device companies of all sizes around the world, inVentiv Health Clinical can help you transform promising ideas into commercial reality.
Post: Sr. Medical Writer
Job Description:
•Work with cross-functional departments e.g. R&D, LOC, regulatory and commercial departments
•Takes responsibility for preparation of assigned documents to a high standard, working in accordance with guidelines and SOPs
•Participates in both internal and external project team meetings and liaises directly with the customer on medical and/or technical writing issues, as appropriate and with senior support as needed.
•May review documents or parts of documents prepared by other Medical Writers and provide appropriate feedback. Gives guidance to less experienced Medical Writers and assists in their training and development.
Responsibilities
•Excellent standard of written English, and ability to communicate fluently and effectively in English, both in writing and verbally.
•In-depth knowledge of the structural and content requirements of regulatory documents and publications
•Ability to integrate, interpret, and summarize data from a variety of sources in a clear and concise manner.
•Demonstrated ability and experience to work independently on most writing projects, with limited senior guidance.
•Good understanding of common statistical methods used in clinical trials or pharmaceutical work and/or interpretation of their results.
•Ability to give a presentation to a project team and/or customer on project-specific topics, with an air of competence and authority.
•Ability to work on several projects at once while balancing multiple and overlapping timelines.
•Ability to assess and prioritize workload.
•Demonstrated abilities in collaboration with others and independent thought.
•Careful attention to detail and accuracy.
•Ability to establish and maintain effective working relationships with coworkers, managers and clients.
•Knowledge/experience with OTC products will be useful
Candidate Profile: Master’s degree in a life science-related discipline, communications, or related field, with at least 4-6 years broad-ranging experience as a medical writer in preparing regulatory and commercial documents
Additional Information:
Experience: 4-6 Years
Location: Gurgaon
Industry Type: Clinical Research
Functional Area: Medical Writing
Last Date: 30th Sep, 2013
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