Medical Writer - PhD - Hematology/Oncology - Cincinnati

Medpace; Cincinnati (OH); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Competitive PTO starting at 20+ days

Company-sponsored employee appreciation events

Discounted tuition for UC online programs

Employee health and wellness initiatives

Job summary

Medpace is seeking a full-time Medical Writer in Cincinnati to develop critical documents for medical therapeutics. Candidates should have a PhD in Life Sciences focused on Hematology or Oncology.

This role includes writing clinical documents, collaborating with experts, and requires strong analytical skills. Benefits include competitive compensation, flexible work arrangements, and numerous development opportunities. This is a unique chance to contribute to the medical field in a supportive and innovative environment.

Qualifications

• Ability to synthesize complex information into a clear format.
• Energetic, enthusiastic, self-motivated, eager to learn and grow.
• Prior experience in the CRO, pharmaceutical, or medical writing industries is advantageous.

Responsibilities

• Write, edit, and maintain high-quality clinical and regulatory documents.
• Coordinate and conduct quality control reviews.
• Communicate and collaborate with Sponsors and Medpace subject matter experts.
• Manage multiple projects while meeting deadlines.
• Maintain compliance with company processes and industry regulations.

Skills

Synthesize complex information

Team player

Analytical skills

Education

PhD in Life Sciences with focus in Hematology and/or Oncology

Job description

Job Summary

Medpace is currently seeking candidates with a PhD in Life Sciences with a focus in Hematology and/or Oncology 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 Hematology and/or Oncology 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.

Benefits

• 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