Senior Medical Content Lead, Regulatory Document Creation
1 week ago
Unlock Your Potential as a Senior Medical Content Lead
Parexel is seeking an experienced Senior Medical Content Lead to lead our medical writing efforts and create high-quality regulatory documents.
About the Role:
The successful candidate will be responsible for researching, creating, and editing documents associated with clinical research. As a project lead writer/submission coordinator and primary client contact, you will manage contributions from multiple writers working on related documents. You will also facilitate process improvement, technical mentoring/training, and support Medical Writing Services management during the sales process by providing client liaison and proposals input.
What We're Looking For:
- A minimum of 10 years of experience in regulatory medical writing, including authoring protocols, clinical study reports, investigator's brochures, informed consent forms, summary documents, and more.
- Proven expertise in multiple therapeutic areas, such as vaccines, immunology, autoimmune disorders, cardiovascular disorders, endocrine disorders, gastrointestinal disorders, infectious diseases, mental health, neurology, oncology, and others.
- Strong communication and interpersonal skills to collaborate with cross-functional teams and clients.
- A bachelor's or advanced degree in life sciences/healthcare, or equivalent education/degree.
- Experience from the pharmaceutical/CRO industry, with a focus on variable workload management.
- A commitment to delivering high-quality outputs with exceptional attention to detail.
Your Benefits:
This role offers a competitive salary of $120,000 - $160,000 per year, depending on experience, plus benefits that include comprehensive health insurance, retirement savings plan, paid time off, and professional development opportunities.
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