Regulatory Start-Up Manager – Clinical Trials

IQVIA; Riyadh; On-site; SAR 180,000 - 240,000; Full time

Job summary

A leading global healthcare company in Saudi Arabia is seeking a Site Activation Manager to manage all aspects of site activation, maintenance, and regulatory activities for clinical studies. The ideal candidate will have 7 years of relevant experience and a Bachelor's degree in Life Sciences, with strong regulatory and technical writing skills. Proficiency in Arabic is essential. This role includes developing management plans, ensuring compliance, and mentoring team members.

Qualifications

• 7 years' relevant experience in a scientific or clinical environment.
• Strong understanding of regulated clinical trial environment.
• In-depth knowledge of drug development process.

Responsibilities

• Oversee Site Activation and Maintenance for assigned projects.
• Develop and maintain the Management Plan according to Scope of Work.
• Ensure collaboration across regions and countries.
• Create and review documentation to support business development.
• Mentor and coach colleagues as required.

Skills

Regulatory experience

Financial experience

Arabic language fluency

Education

Bachelor's Degree in Life Sciences or related field

Job description

A leading global healthcare company in Saudi Arabia is seeking a Site Activation Manager to manage all aspects of site activation, maintenance, and regulatory activities for clinical studies. The ideal candidate will have 7 years of relevant experience and a Bachelor's degree in Life Sciences, with strong regulatory and technical writing skills. Proficiency in Arabic is essential. This role includes developing management plans, ensuring compliance, and mentoring team members.