- 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