Medical Writer - PhD - Cardiovascular/Metabolic - Cincinnati

Medpace; Cincinnati (OH); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Comprehensive training

Job summary

Medpace is currently seeking candidates for a full-time, office-based Medical Writer position. This role requires a PhD in Life Sciences focusing on Cardiovascular and/or Metabolic research and involves writing, editing, and maintaining high-quality clinical documents critical to medical therapeutics development.

The position offers comprehensive training, project management, and collaborative work with subject matter experts, providing a unique opportunity for those looking to excel in the pharmaceutical and medical device fields.

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.

Responsibilities

• Write, edit, and maintain high-quality, complex clinical and regulatory documents.
• 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.
• Maintain an understanding of and compliance with company processes, and industry guidelines and regulations.

Skills

Analytical skills

Synthesize complex information

Team collaboration

Education

PhD in Life Sciences with a focus in Cardiovascular and/or Metabolic research

Job description

Job Summary

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.
• 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.
• Prior experience in the CRO, pharmaceutical, or medical writing industries is not required but is advantageous.