Madrigal Pharmaceuticals
Pharmaceuticals • Biotechnology • Healthcare Insurance
Madrigal Pharmaceuticals is a biopharmaceutical company focused on developing novel therapeutics for nonalcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). The company achieved a significant milestone with the accelerated FDA approval of its first therapy for adults with NASH with moderate to advanced liver fibrosis. Madrigal is actively conducting a Phase 3 trial for the treatment of NASH with compensated cirrhosis. The company is dedicated to improving care for patients with NASH/MASH through its ambitious research programs and therapeutic developments.
51 - 200 employees
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $259M Post-IPO Equity on 2022-12
Associate Director, Medical Writing
Job not on LinkedIn
October 28
🍂 Massachusetts – Remote
💵 $173k - $211k / year
⏰ Full Time
🟠 Senior
✏️ Content Writer
🦅 H1B Visa Sponsor
Madrigal Pharmaceuticals
Pharmaceuticals • Biotechnology • Healthcare Insurance
Madrigal Pharmaceuticals is a biopharmaceutical company focused on developing novel therapeutics for nonalcoholic steatohepatitis (NASH), also known as metabolic dysfunction associated steatohepatitis (MASH). The company achieved a significant milestone with the accelerated FDA approval of its first therapy for adults with NASH with moderate to advanced liver fibrosis. Madrigal is actively conducting a Phase 3 trial for the treatment of NASH with compensated cirrhosis. The company is dedicated to improving care for patients with NASH/MASH through its ambitious research programs and therapeutic developments.
51 - 200 employees
💊 Pharmaceuticals
🧬 Biotechnology
⚕️ Healthcare Insurance
💰 $259M Post-IPO Equity on 2022-12
📋 Description
• Write documents supporting Phase 1 through IV clinical trials • Collaborate closely with cross-functional teams • Ensure that documents are of the highest quality and compliant with global regulatory requirements • Contribute to updates to standard operating procedures • Stay current with regulatory guidelines, industry trends, and best practices in medical writing
🎯 Requirements
• 6+ years of clinical or regulatory medical writing experience • Strong understanding of drug development process, including clinical research, regulatory requirements, and publication strategies • Experience in liver, cardiovascular or metabolic diseases • Familiarity with designing and operationalizing clinical studies • Able to analyze and interpret complex clinical data and scientific information • Experienced in using industry standard technical tools (e.g., Microsoft Word macros) • Committed to adhere to ethical principles and industry standards, including Good Clinical Practice (GCP) and Good Documentation Practices (GDP)
🏖️ Benefits
• Flexible paid time off • Medical insurance • Dental insurance • Vision insurance • Life/disability insurance • 401(k) offerings (traditional, Roth, employer match) • Supplemental life insurance • Legal services • Mental health benefits through Employee Assistance Program
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