Sponsor Site Activation & Regulatory Lead

IQVIA; Durham (NC); On-site; USD 60,000 - 157,000; Full time

Job summary

IQVIA, a global leader in clinical research services, seeks a Site Activation professional in Durham, NC. The role focuses on start-up meetings, regulatory document preparation, and tracking project timelines, ensuring SOP compliance.

Ideal candidates hold a life sciences degree with clinical research experience and strong communication, negotiation, and organizational skills. This position requires independent work and effective prioritization in a fast-paced environment.

Qualifications

• Bachelor's degree in life sciences or related field; 3 years of clinical research or equivalent experience.
• Experience in leadership roles within clinical research.
• Knowledge of GCP/ICH and regulatory guidelines.

Responsibilities

• Act as Single Point of Contact for sites, SAMs, and project teams to ensure SOP and project timelines adherence.
• Lead start-up and site activation activities in line with regulations and SOPs.
• Prepare site regulatory documents and review for completeness.
• Maintain internal systems with project-specific information.
• Provide site performance feedback to management and track progress of documents.
• Support project planning and contingency planning with timelines.

Skills

Negotiation skills

Communication skills

Organizational skills

Independent work

Task prioritization

Education

Bachelor's Degree in life sciences

3 years clinical research experience

Job description

IQVIA, a global leader in clinical research services, seeks a Site Activation professional in Durham, NC. The role focuses on start-up meetings, regulatory document preparation, and tracking project timelines, ensuring SOP compliance.

Ideal candidates hold a life sciences degree with clinical research experience and strong communication, negotiation, and organizational skills. This position requires independent work and effective prioritization in a fast-paced environment.