IQVIA job vacancy for Medical Writing Trainee – Apply Now
Job Type: Full-Time
Job Responsibilities:
Job Family Description:
Writes, reviews, and coordinates preparation of clinical trial documentation in line with client specifications and industry practices.
Sub-Family Description
Prepares, or contributes to the preparation of clinical and regulatory documents for external clients, for investigational drugs, biologicals, or medical devices.
Collaborates with internal and external experts and specialists and maintains expertise on developments in a particular field of focus.
JOB OVERVIEW
Job Profile Summary
An entry level role within a structured program, supporting Medical Writing deliverables and focusing on specific tasks under senior supervision, while gaining experience, knowledge, and skills in Medical Writing.
Keeps abreast of current medical and/or technical writing/regulatory knowledge, including GCP, along with developments and advances in drug development/medical and/or technical writing.
Responsibilities
Essential Functions
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Gain knowledge, experience, and competence in specific Medical Writing tasks by supporting Medical Writing senior staff in managing client requests under supervision, focusing on tasks such as writing patient narratives.
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Manage day-to-day workload, track timelines, draft assigned documents to a high standard, and implement review comments and customer requests with senior guidance/review, keeping manager/senior staff abreast of progress on tasks and any potential problems.
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Interact with internal clients. May have some external interactions, mostly directed by senior staff.
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Keep abreast of current data, trends, medical and/or technical writing/regulatory knowledge, developments and advances in area of drug development/medical and/or technical writing.
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