LatAm Site Activation Specialist | Regulatory & Feasibility

IQVIA; United States; Remote; USD 70,000 - 110,000; Full time

Job summary

IQVIA is seeking a country-level Site Activation Specialist to support SA activities in accordance with local and international regulations and SOPs. You will work under moderate supervision, act as SPOC for investigative sites, SAM, and project teams, and help ensure timely delivery of startup documentation.

Responsibilities include feasibility studies, site ID and activation, document preparation and QA, and coordination of regulatory submissions.

Qualifications

• Bachelor's degree in life sciences or related field.
• Minimum 3 years of clinical research experience supporting site activation and regulatory tasks.
• Advanced English required for global collaboration.

Responsibilities

• Serve as SPOC for investigative sites, SAM, PM team and other departments.
• Perform feasibility, site ID, start-up and activation activities per regulations.
• Prepare site documents, reviewing for completeness and accuracy.
• Maintain internal systems and tracking tools with project data.
• Review site performance metrics and provide feedback to management.
• Ensure project plans and timelines are in place with contingency plans.
• Coordinate regulatory and contract documents release per timelines.
• Provide local expertise during project planning.
• Perform quality control of documents provided by sites.
• May interact with sponsors on specific initiatives.

Skills

Advanced English

SPOC for sites

Education

Bachelor’s Degree Life science or related field

Job description

IQVIA is seeking a country-level Site Activation Specialist to support SA activities in accordance with local and international regulations and SOPs. You will work under moderate supervision, act as SPOC for investigative sites, SAM, and project teams, and help ensure timely delivery of startup documentation.

Responsibilities include feasibility studies, site ID and activation, document preparation and QA, and coordination of regulatory submissions.