Site Activation Specialist
hace 4 semanas
At Iqvia Llc, we are seeking a highly skilled Site Activation Specialist to join our team. As a key member of our clinical research team, you will be responsible for performing tasks at a country level associated with Site Activation (SA) activities.
Key Responsibilities:
- Work with clinical study teams to ensure the accuracy of data in CTMS
- Provide support to clinical systems end users, including receipt, evaluation, and recommendation for all issue/enhancement requests
- Conduct research and data analysis to identify potential sites that meet the study criteria and objectives
- Assist with feasibility launch, including system set-up, feasibility questionnaire creation, and site-level feasibility questionnaire outreach
- Effectively communicate with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities
- Track and enter data of feasibility responses and report responses to internal stakeholders
- Troubleshoot any issues or discrepancies that arise in the feasibility process
Requirements:
- Bachelor's Degree in Life Science or Scientific Health Field
- 3 years clinical research conducting clinical trials and processes, preferably with North America (sites)
- 2 years of feasibility and recruitment experience
- Experience with trial optimization vendors, tools, and methods
- Analytical thinker, attention to detail, and good communication skills
- Highly proficient with Excel
- Fluent in English
About Iqvia Llc:
Iqvia Llc 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.
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