Associate Medical Writer
New
J
JobgetherClinical research
Remote work options in IndiaFull-TimeJunior
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Languages
- Excellent English communication skills
- Experience
- At least 1 year of medical writing experience is preferred. At least 2 years of experience in pharmaceutical, biotechnology, clinical research, healthcare, medical imaging, or a related industry is preferred.
- Required Skills
- Microsoft ExcelPowerPoint
Requirements
- A bachelor’s degree in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare, Clinical Research, or a related scientific discipline is preferred.
- At least 1 year of medical writing experience is preferred; equivalent clinical research or scientific documentation experience may be considered.
- At least 2 years of experience in pharmaceutical, biotechnology, clinical research, healthcare, medical imaging, or a related industry is preferred.
- Understand medical writing, scientific documentation, clinical research principles, and relevant regulatory requirements.
- Knowledge of clinical trial terminology, clinical research processes, and medical imaging concepts is an advantage.
- Have strong working knowledge of Microsoft Word, Excel, PowerPoint, and Outlook.
- Have excellent English communication skills and the ability to prepare clear, accurate, well-structured scientific and operational documents.
- Demonstrate proofreading, editing, and document review skills with attention to accuracy, consistency, and compliance.
- Manage multiple projects, competing priorities, and deadlines while maintaining quality deliverables.
- Work independently and collaborate effectively with cross-functional, geographically distributed teams.
Responsibilities
- Prepare, organize, and maintain study-specific medical writing and medical communications documentation for study startup.
- Review clinical study protocols and imaging requirements to understand study procedures, schedules, and operational expectations.
- Create, update, review, and finalize site manuals, supporting forms, labels, and study-specific communication materials.
- Prepare and maintain Notes to File, protocol amendment impact assessments, correction records, and other quality and compliance documentation.
- Develop and maintain source documents and electronic clinical forms for study execution.
- Prepare agendas, meeting minutes, and action item records for study startup, project meetings, and medical communications activities.
- Maintain medical communications resources, databases, web content, document repositories, and study tracking tools.
- Support study closeout and archive documentation according to established procedures and applicable regulatory requirements.
- Assist with SOPs, work instructions, templates, training materials, and reader training content.
View Full Description & ApplyYou'll be redirected to the employer's site
