Senior Site Activation & Feasibility Lead

IQVIA; Buenos Aires; Presencial; ARS 1.200.000 - 2.000.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a country-level Site Activation professional to manage feasibility, site initiation, and activation activities in accordance with local and international regulations and SOPs. The role supports SAMs, PM teams, and other departments, ensuring timely, accurate documentation and ongoing process improvements.

You will review timelines, maintain systems and databases, and provide local expertise during project planning.

Formación

• Bachelor's Degree Life science or related field required.
• 3 years clinical research experience, including 1 year leadership experience required.
• Equivalent combination of education, training and experience may be acceptable.

Responsabilidades

• Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary. Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
• Perform feasibility, site ID, start up and site activation activities according to applicable regulations, SOPs and work instructions. Distribute completed documents to sites and internal project team members.
• Prepare site documents, reviewing for completeness and accuracy.
• Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
• Review and provide feedback to management on site performance metrics.
• Review, establish and agree on project planning and project timelines. Ensure monitoring measures are in place and implement contingency plan as needed.
• Inform team members of completion of fesibility, site ID, regulatory and contractual documents for individual sites.
• Review, track and follow up the progress, the approval and execution of documents, questionnaires, CDA/SIF, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
• Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
• Perform quality control of documents provided by sites.
• May have direct contact with sponsors on specific initiatives.

Educación

Bachelor's Degree Life science or related field

3 years clinical research experience, including 1 year experience in a leadership capacity.

3 years clinical research or other relevant experience; or equivalent combination of education, training and experience.

Descripción del empleo

IQVIA is seeking a country-level Site Activation professional to manage feasibility, site initiation, and activation activities in accordance with local and international regulations and SOPs. The role supports SAMs, PM teams, and other departments, ensuring timely, accurate documentation and ongoing process improvements.

You will review timelines, maintain systems and databases, and provide local expertise during project planning.