Clinical Operations Lead – Regulatory & Site Activation

Iqvia; As Sudiyah; On-site; OMR 30,000 - 50,000; Full time

Job summary

A leading clinical research organization is seeking a candidate to manage site activation and regulatory activities for clinical studies in Oman. The ideal candidate should have a Bachelor's Degree in Life Sciences and at least 7 years of relevant experience in a scientific or clinical environment, demonstrating strong regulatory skills and Arabic fluency. Responsibilities include overseeing regulatory submissions, managing contracts, and providing overall strategic regulatory guidance. Office presence is required 3-4 times a week.

Qualifications

• 7 years of relevant experience in a scientific or clinical environment, including international roles.
• Thorough understanding of the regulated clinical trial environment and in-depth knowledge of drug development.
• Ability to apply ICH guidelines and applicable regulatory guidelines.

Responsibilities

• Direct the delivery of site activation and maintenance activities for clinical studies.
• Oversee regulatory submissions and contract management.
• Provide regulatory and technical support to facilitate compliance.

Skills

Regulatory activities management

Financial management

Arabic language fluency

Clinical Practice (GCP) knowledge

Technical writing skills

Education

Bachelor's Degree in Life Sciences or related field

Job description

A leading clinical research organization is seeking a candidate to manage site activation and regulatory activities for clinical studies in Oman. The ideal candidate should have a Bachelor's Degree in Life Sciences and at least 7 years of relevant experience in a scientific or clinical environment, demonstrating strong regulatory skills and Arabic fluency. Responsibilities include overseeing regulatory submissions, managing contracts, and providing overall strategic regulatory guidance. Office presence is required 3-4 times a week.