Medical Writer I (1 Year Fixed Term)
0 - 1 YearsHyderabad / Secunderabad
Job Description
- Contribute to the develop of clinical regulatory documents,such as study reports, protocols, Master Informed Consent forms, investigator brochures, medical information letters, press releases, patient brochures and etc.
- Develop tables, charts, figures, and other display elements for clinical data.
- Contribute to document quality checks, formatting, and comment consolidation.
- Address team comments accurately to ensure document scientific content, clarity, overall consistency, and proper format.
- Comply with client or company procedures for completing deliverables, obtaining reviews, incorporating edits, and working with teams to complete/finalize deliverables.
- Keep supervisor and team members informed of project status and participate in team meetings.
- Working knowledge of drug development process and regulatory guidelines.
- Continue professional development to keep pace with regulatory guidance and client expectations, and to improve skills.
- Stay aware of the budget specifications for all assigned projects, working within the budgeted hours and communicating any changes to medical writing leadership.
- Complete all administrative tasks within specified timeframes.
Company Profile
inVentiv Health Clinical is a leading provider of global drug development services to pharmaceutical, biotechnology, generic drug, and medical device companies. With 6,500 passionate employees supporting clients in more than 70 countries, inVentiv Health Clinical works to accelerate high quality drug development programs of all sizes around the world.
Like you, we are committed to enriching the lives of patients, families, and communities by helping to expedite the quality delivery of our clients' therapies to market.
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