Site Activation Specialist: Start-Up & Feasibility

IQVIA; United States; Remote; USD 55,000 - 75,000; Full time

Job summary

IQVIA is seeking a junior professional to support site activation activities and feasibility for North American sites. The role involves coordinating regulatory documents, coordinating with the Site Activation Manager and project teams, and ensuring timely completion of site documentation.

Under supervision, you will prepare documents, track progress, and maintain project plans. This entry-level position offers growth within a global clinical research leader and exposure to diverse studies.

Qualifications

• Bachelor's degree in life sciences or a related field.
• At least 1 year of clinical research experience.
• Advanced English proficiency for North American sites.

Responsibilities

• Serve as SPOC for feasibility and site activation activities for investigative sites.
• Prepare and review site documents for completeness and accuracy.
• Inform team when regulatory and other documents are complete.
• Distribute documents to sites and internal project teams.
• Update internal systems with project information and timelines.
• Track progress and execution of required documents (CDA, regulatory, ethics, ICF, IP).

Skills

English (Advanced)

Education

Bachelor's Degree in Life Sciences

Job description

IQVIA is seeking a junior professional to support site activation activities and feasibility for North American sites. The role involves coordinating regulatory documents, coordinating with the Site Activation Manager and project teams, and ensuring timely completion of site documentation.

Under supervision, you will prepare documents, track progress, and maintain project plans. This entry-level position offers growth within a global clinical research leader and exposure to diverse studies.