The 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, investigator’s 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.
Apply: https://jobs.parexel.com/en/job/india/senior-medical-writer/877/76035019824