CLIENT SUMMARY

A global leader in research-based drug development, this CRO builds strong strategic partnerships with select Sponsors to advance the most efficient and cost-effective path to drug approval. As a therapeutically-focused Clinical Research Organization (CRO), it is viewed as a steward of drugs, leveraging extensive medical and regulatory expertise to deliver additional input, strategy, and efficiencies to each and every phase of the clinical trial. From custom solutions addressing the needs of small and midsize biotechnology companies to full-service offerings for global pharmaceutical companies, the company has the breadth, depth, and flexibility to deliver a superior result, specific to client needs, on six continents.

JOB SUMMARY

The medical writer will be interacting closely with multiple operational units of the business to assist in documenting the outcome of various projects.  Essential is the ability to compose technical information in a format that is easily understood by the layman.

KEY JOB RESPONSIBILITIES

• Writing clinical study reports, integrated summaries of efficacy and safety, and protocols.
• Coordinating quality assurance reviews of documents and maintaining audit trails of changes.
• Providing input on data analysis planning and interpretation.

IDEAL CANDIDATES’ QUALIFICATIONS AND EXPERIENCE

Candidate with a Bachelor degree in journalism, English or related.  Candidate should have a minimum of at least 5 years of true medical writing experience.  Prior experience in the healthcare industry required.         

ADDITIONAL COMMENTS

The selected candidate must be in Cincinnati or willing to relocate to Cincinnati.  No remote working arrangements.