Life Sciences Content Specialist

1 day ago

kochi, India beBeeRegulatoryMedicalWriter Full time

A regulatory medical writer is responsible for drafting, reviewing and finalizing clinical study reports, investigator brochures and other key documents. The role requires strong organizational skills, attention to detail and excellent collaboration and communication skills.Key Responsibilities:Literature reviewsRegulatory complianceCross-functional team collaborationScientific content quality assuranceThe ideal candidate will possess an advanced degree in life sciences, pharmacy or a related scientific field along with prior experience in the pharmaceutical, biotechnology or clinical research industry. Advanced proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) is required.Required Skills and Qualifications:Advanced degree in life sciences, pharmacy or a related fieldPrior experience in the pharmaceutical, biotechnology or clinical research industryStrong organizational and communication skillsAttention to detail and ability to work independentlyBenefits of Working as a Regulatory Medical Writer:Contribute to the development of critical healthcare productsCollaborate with cross-functional teams to achieve project goalsOpportunity for professional growth and developmentAbout this Role:This is a challenging and rewarding role that requires a unique blend of scientific knowledge, technical skills and business acumen. If you are a motivated and detail-oriented individual with a passion for scientific writing, we encourage you to apply.

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