Community involvement with local nonprofit organizations
Discounts on local sports games
Modern, eco-friendly campus with fitness center
Discounted tuition for UC online programs
Job summary
A leading clinical contract research organization in Cincinnati is seeking a full-time Regulatory Submissions Coordinator. This entry-level position involves coordinating regulatory submissions, maintaining quality review of trial documents, and working with research sites. Candidates should have a PharmD, possess strong organizational and communication skills, and be detail-oriented. The company offers a robust training program and a positive work culture with opportunities for growth.
Qualifications
PharmD required, preferably in Life Sciences.
3.5 GPA or above preferred.
Some office experience is preferred.
Responsibilities
Communicate with research sites to collect essential documents.
Maintain ongoing quality review of trial documents.
Collect and assemble regulatory start-up submissions.
Maintain study start-up timelines.
Review regulations to develop solutions.
Skills
Organizational skills
Communication skills
Attention to detail
Prioritization skills
Education
PharmD
Tools
Microsoft Office
Job description
A leading clinical contract research organization in Cincinnati is seeking a full-time Regulatory Submissions Coordinator. This entry-level position involves coordinating regulatory submissions, maintaining quality review of trial documents, and working with research sites. Candidates should have a PharmD, possess strong organizational and communication skills, and be detail-oriented. The company offers a robust training program and a positive work culture with opportunities for growth.