Global Head, Medical Affairs & Clinical Trials

CTI Clinical Trial and Consulting Services; Covington (KY); On-site; USD 120,000 - 180,000; Full time

Job summary

CTI Clinical Trial and Consulting Services is seeking a qualified individual to lead global Medical Affairs and RSA teams in Covington, Kentucky. The ideal candidate will have 15 years of pharmaceutical and regulatory experience, along with a Master’s, PhD, or MD.

This role will focus on developing and managing global business plans while ensuring all project deliverables are met according to ethical standards. A strong background in team leadership and scientific writing is essential.

Qualifications

• 15 years of pharmaceutical / CRO, drug development, regulatory experience.
• Scientific, regulatory, clinical trial or drug development experience.
• Thorough knowledge of relevant FDA and other health authorities’ regulations.

Responsibilities

• Lead global Medical Affairs and RSA teams.
• Develop and maintain departmental global business plans.
• Ensure projects are completed according to contractual agreements.
• Oversee and review processes for deliverables with quality oversight.
• Develop and manage department budgets.

Skills

Leadership

Project management

Regulatory knowledge

Scientific writing

Team building

Education

Master’s, PhD, or MD

Job description

CTI Clinical Trial and Consulting Services is seeking a qualified individual to lead global Medical Affairs and RSA teams in Covington, Kentucky. The ideal candidate will have 15 years of pharmaceutical and regulatory experience, along with a Master’s, PhD, or MD.

This role will focus on developing and managing global business plans while ensuring all project deliverables are met according to ethical standards. A strong background in team leadership and scientific writing is essential.