Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati

Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research for a full-time, office-based Medical Writer position. The Medical Writer will lead development of various high-quality documents critical to the development of safe and effective medical therapeutics. This is a unique opportunity that includes comprehensive training and application of the candidate’s analytical skills and academic knowledge . The position includes independent work and cross-functional collaboration. If you want a rewarding position that allows you to be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Responsibilities

• Write, edit, and maintain high-quality, complex clinical and regulatory documents, including, but not limited to, clinical study reports, protocols, Investigator’s brochures, and IND and NDA modules;
• Coordinate and conduct quality control reviews;
• Effectively communicate and collaborate with Sponsors and Medpace subject matter experts;
• Manage multiple projects and tasks simultaneously while also meeting deadlines; and
• Maintain an understanding of and compliance with company processes, and industry guidelines and regulations.

Qualifications

• PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical);
• Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience;
• Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and
• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous.

Medpace Overview

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Why Medpace?

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Cincinnati Perks

• Cincinnati Campus Overview
• Flexible work environment
• Competitive PTO packages, starting at 20+ days
• Competitive compensation and benefits package
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives
• Community involvement with local nonprofit organizations
• Discounts on local sports games, fitness gyms and attractions
• Modern, ecofriendly campus with an on-site fitness center
• Structured career paths with opportunities for professional growth
• Discounted tuition for UC online programs

Awards

•

Named a Top Workplace in 2024 by The Cincinnati Enquirer

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.

• Write, edit, and maintain high-quality, complex clinical and regulatory documents, including, but not limited to, clinical study reports, protocols, Investigator's brochures, and IND and NDA modules; • Coordinate and conduct quality control reviews; • Effectively communicate and collaborate with Sponsors and Medpace subject matter experts; • Manage multiple projects and tasks simultaneously while also meeting deadlines; and • Maintain an understanding of and compliance with company processes, and industry guidelines and regulations.

• PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research (clinical or nonclinical); • Ability to synthesize complex information into a clear and concise format that is appropriate for the target audience; • Energetic and enthusiastic team-player that is self-motivated and eager to learn and grow in the position; and • Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous.