What are the responsibilities and job description for the Clinical Documentation Expert position at Madrigal Pharmaceuticals Corporation?
Welcome to Madrigal Pharmaceuticals Corporation, a leading biopharmaceutical company focused on developing novel therapeutics for NASH and other metabolic disorders.
We are currently seeking an experienced Medical Writer to lead our medical writing efforts. As a key member of our team, you will be responsible for ensuring the accuracy, consistency, and quality of clinical and regulatory documents.
Key Responsibilities:
- Develop and implement medical writing strategies to support Phase 1 through IV clinical trials.
- Collaborate with cross-functional teams to ensure alignment between medical writing activities and program goals.
- Prepare high-quality clinical and regulatory documents, including protocols, reports, and submissions.
Qualifications:
- 10 years of experience in medical writing, preferably in pharmaceutical drug development.
- Strong understanding of regulatory requirements, including GCP and GDP.
- Excellent communication and project management skills.
What We Offer:
We offer a competitive salary and comprehensive benefits package, including flexible paid time off, medical, dental, vision, and life and disability insurance.
Madrigal Pharmaceuticals Corporation is an equal opportunity employer committed to diversity and inclusion.
