- Perform allied activities such as data collection for report planning, developing strategy, and leading kick-off meetings and round table discussions for comment resolution.
- Write various safety reports (or part of such reports) for global regulatory submissions, including but not limited to Annual Reports (IND and other), Periodic Safety Update Reports, Periodic Adverse Drug Experience Reports, Development Safety Update Report, Risk Management Plans, and other documents. Take ownership of the assigned deliverables and collaborate with internal/client stakeholders and the client to get the required inputs.
- Perform quality review of the safety reports prepared by junior or associate medical writers.
- Author or contribute to ad hoc reports, benefit-risk evaluation reports, justification/supporting documents for label updates.
- Write Common Technical Document Summaries including Non-Clinical and Clinical Overviews, Clinical Summaries, and other regulatory documents as assigned.
- Prepare medical information responses for HCPs.
- Author/contribute to signal reports (ad hoc & periodic) & safety issue analysis reports.
- Write subject narratives for adverse drug reactions and serious adverse events.
- Internal and external (client) communication & coordination to get the required inputs.
- Participate in creating and updating labels, e.g., Core Data Sheets, USPI, centralized SPCs, Med Guides.
- Conduct literature searches for authoring various types of reports or routine surveillance activities. Review and propose updates needed if any to the search strategies. Review the articles selected by other medical writers/junior writers. Author literature abstracts/summaries and propose Company comments.
- Implement and promote the use of consistent, efficient, and quality processes to meet timelines and deliverables according to requirements and standard operating procedures and assume accountability for the deliverables.
- Ensure compliance of operations with governing regulatory requirements.
- Create, maintain, and assume accountability for a culture of high customer service.
- Perform any additional activities as per the project requirement or manager’s discretion on completion of relevant training.
Are you a recent graduate looking to kickstart your career in pharmaceutical writing? Fortrea, a global contract research organization (CRO), is offering Safety Writer fresher vacancies in Mumbai, India. This is an excellent opportunity to join a dynamic team and contribute to groundbreaking clinical development projects.
Safety Writer Fresher vacancies - Fortrea
Safety Writer
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Locations: Mumbai, India
Time Type: Full-time
Posted on: Posted Yesterday
Job Requisition ID: 2370185
As a leading global contract research organization (CRO) with a passion for scientific rigor and decades of clinical development experience, Fortrea provides pharmaceutical, biotechnology, and medical device customers a wide range of clinical development, patient access, and technology solutions across more than 20 therapeutic areas. With over 19,000 staff conducting operations in more than 90 countries, Fortrea is transforming drug and device development for partners and patients across the globe.
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