About the jobThe Senior Medical Writer will research, create, and edit all documents associated with clinical research. The Senior Medical Writer may operate as the project lead writer/submission coordinator and primary client contact to manage contributions of multiple writers working on related documents. The Senior Medical Writer also facilitates process improvement and technical mentoring/training and supports Medical Writing Services management during the sales process by providing client liaison and proposals input.
Minimum Qualification Requirements
- Candidate must have 6+ have experience in regulatory medical writing. Experience in authoring protocols, clinical study reports, investigators brochures, informed consent forms, summary documents, etc.
- Experience in multiple therapeutic areas, including but not limited to vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders, gastrointestinal disorders, infectious diseases, mental health, neurology oncology, etc.
- Strong communication and interpersonal skills.
- Bachelors/advanced degree or equivalent education/degree in life sciences/healthcare.
- Experience from the pharmaceutical /CRO industry.
- Ability to work independently and lead projects.
- Strong analytical skills.
- Commitment to highest quality outputs, including high attention to detail.
- Ability to manage variable workload.
Lifelancer ( https://lifelancer.com ) is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech, data science and IT domains.
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https://lifelancer.com/jobs/view/27b33e3da2a566ea812f1f94f3adff29 
