Global Study Start-Up Director & Regulatory Lead

Medpace; Cincinnati (OH); On-site; USD 100,000 - 150,000; Full time

Benefits offered by this job

Flexible work environment

Competitive PTO packages

Employee health and wellness initiatives

Discounted tuition for UC online programs

Job summary

A leading clinical contract research organization is seeking a Director of Study Start-Up to lead the Study Start-Up/Regulatory Submissions team. The role demands extensive experience in a CRO, excellent leadership and negotiation skills, and a strong focus on customer relations. This position is office-based in Cincinnati and offers competitive benefits including bonuses and a flexible work environment. Join a company recognized as a top workplace and contribute to impactful medical advancements.

Qualifications

• 8+ years as a study start-up senior leader within a CRO.
• Experience managing and developing a team.
• Ability to manage challenging priorities.

Responsibilities

• Contribute to the growth and strategic development of a large, global Study Start-Up team.
• Develop and identify continuous improvement opportunities.
• Oversee Study Start-Up/Regulatory Submissions activities and timelines.

Skills

Presentation skills

Negotiation skills

Leadership

Interpersonal skills

Customer focus

Education

Bachelor’s degree in Life Sciences

Advanced degree (preferred)

Job description

A leading clinical contract research organization is seeking a Director of Study Start-Up to lead the Study Start-Up/Regulatory Submissions team. The role demands extensive experience in a CRO, excellent leadership and negotiation skills, and a strong focus on customer relations. This position is office-based in Cincinnati and offers competitive benefits including bonuses and a flexible work environment. Join a company recognized as a top workplace and contribute to impactful medical advancements.