Study Start-Up Coordinator – Regulatory Submissions

Medpace; Cincinnati (OH); On-site; USD 50,000 - 70,000; Full time

Job summary

A clinical research organization is seeking a full-time Regulatory Submissions Coordinator in Cincinnati, Ohio. This role involves coordinating regulatory submissions, ensuring compliance, and communicating with research sites. Ideal candidates will have a Bachelor's degree in Life Sciences and at least 1-5 years of experience in study coordination or the pharmaceutical industry. Strong organizational and communication skills are essential. Join a team dedicated to advancing clinical trials with your expertise.

Qualifications

• Minimum of 1-5+ years of experience as a study coordinator or related pharmaceutical experience required.
• Excellent at organizing and prioritizing tasks.
• Strong written and oral communication skills.

Responsibilities

• Communicate with research sites to collect essential documents for clinical trials.
• Maintain ongoing quality review of trial documents.
• Organize and assemble regulatory submissions.
• Ensure compliance with regulations and requirements.

Skills

Organizational skills

Oral and written communication skills

Attention to detail

Microsoft Office knowledge

Education

Bachelor's degree in a Life Sciences field

Job description

A clinical research organization is seeking a full-time Regulatory Submissions Coordinator in Cincinnati, Ohio. This role involves coordinating regulatory submissions, ensuring compliance, and communicating with research sites. Ideal candidates will have a Bachelor's degree in Life Sciences and at least 1-5 years of experience in study coordination or the pharmaceutical industry. Strong organizational and communication skills are essential. Join a team dedicated to advancing clinical trials with your expertise.