Understanding and undertaking research on the topic given and creating the conceptual framework.
Work closely with the study team and ensure that results in the documents accurately reflect the client s requirement.
Work closely with the study team to reach the consensus on timelines for deliverables.
Complete documents according to agreed-upon timelines and follows up with study team to ensure SOP and regulatory compliances.
Align with the study team to meet the project-related goals.
Rewrite the content if the content fails to fulfil the requirement of the client.
Rephrasing and proofreading the documents if required.
Assisting other academic writing tasks.
Thorough knowledge of clinical research concept, practices and medical writing standards.
Ability to work independently with minimal supervision, do multi-tasks and work effectively under pressure.
Should possess project management, interpersonal and active listening skills.
Should maintain productive and professional working relationship with the team members.
Knowledge in Medical Devices, Pharmaceutical, Food & Life Science
Plan, schedule and manage project deliverables
Working on client requirements - on-time delivery and quality
Read content and correct for errors in spelling, punctuation, and grammar
Rewrite copy to make it easier for readers to understand
Required Skills:
Knowledge in Medical Devices, Pharmaceutical, Food & Life Science
Both Male & Female candidates preferable
Excellent communication with interpersonal skills
Excellent in writing skills
Required Experience: 2 years. Required Qualification: M.B.A., Healthcare Management / or M.Sc., Life Science in relevant subject matter /domain expertise. Department: Production Service Management Work Schedule : Full Time (Flexible Timings), Monday - Saturday (except second Saturday) Location: Chennai