$70.00 - $85.00 /Hour
Remote Contract Medical Writer
Location: Home-based (company office located in Holliston, MA)
Job Type: Full-Time
Duration: 3-6 months contract (possible contract extension)
Compensation: Open to discussion
Summary of Job Responsibilities:
The Medical Writer will Write Patient Narratives for phase III oncology trials
Adhere to sponsor’s template and format for all narratives
Meets critical project deadlines and submit work in a timely fashion
Be able to write high quality, detailed, lengthy, and scientifically accurate patient narratives
The Medical Writer Works independently with the sponsor representative with regard to document planning, review, revision, and finalization.
Minimum Education: BS/BSc/BA in a science or industry-related discipline. Minimum Work Requirements: Minimum of 5 years of medical writing experience in a CRO, pharmaceutical, or biotechnology setting. Other professional and/or educational experience may contribute toward this minimum requirement, as determined on a case-by-case basis.
Skills: Working knowledge of ICH and other regulatory guidelines required. The ability to accurately and clearly present clinical data, strong verbal, written, and interpersonal communication skills, and proficiency in Microsoft Word required. Broad knowledge of global pharmaceutical regulatory requirements required, and experience in clinical research or other areas of the pharmaceutical industry preferred.
Excellent regulatory writing skills (e.g., English usage), and a keen attention to detail also are required.
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