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About the Role

Perform country-level Site Activation (SA) activities in accordance with regulations, SOPs, project requirements, and contractual/budgetary guidelines. This role involves developing professional individual contributor skills with moderate oversight, making recommendations for system and process enhancements, and addressing general but not complex issues.

Responsibilities

• Serve as Single Point of Contact (SPOC) for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments.
• Ensure adherence to SOPs, Work Instructions (WIs), quality of deliverables, and project timelines.
• Perform feasibility, site ID, start-up, and site activation activities.
• Distribute completed documents to sites and internal project team members.
• Prepare and review site documents for completeness and accuracy.
• Ensure accurate completion and maintenance of internal systems, databases, and tracking tools.
• Review and provide feedback to management on site performance metrics.
• Review, establish, and agree on project planning and timelines.
• Ensure monitoring measures are in place and implement contingency plans as needed.
• Inform team members of the completion of feasibility, site ID, regulatory, and contractual documents.
• Review, track, and follow up on the progress of documents, questionnaires, CDA/SIF, regulatory, ethics, ICF, and IP release documents.
• Provide local expertise to SAMs and project team during planning.
• Perform quality control of documents provided by sites.
• May have direct contact with sponsors on specific initiatives.

Requirements

• Bachelor's Degree in Life science or related field.
• 3 years of clinical research or other relevant experience, or equivalent combination of education, training, and experience.
• 3 years clinical research experience, including 1 year in a leadership capacity.

Work Type

• full-time

Experience Level

• Entry Level
• Mid-Level

Education Level

• Bachelor's Degree

Salary/Compensations

• $78,800.00 - $105,000.00

Benefits

• Health and wellness benefits
• Other benefits

About the Company

• IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries.
• We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
• Learn more at https://jobs.iqvia.com

Equal Opportunity

• IQVIA is proud to be an equal opportunity employer.
• All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law.
• Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request.
• If you have a disability that requires an accommodation, we encourage you to contact our Talent Acquisition Team at: workday_recruiting@iqvia.com, so that IQVIA can support your participation in the recruitment process.
• IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
• All information and credentials submitted in your application must be truthful and complete.
• Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
• We appreciate your honesty and professionalism.
• Please note that we may use artificial intelligence (AI) in the processing of your application.
• However, we only use AI to assist our recruitment team with the screening or assessment of candidacies, and not as a substitute for human decision-making.