Site Selection Specialist

IRE

5d • Remote

About The Position

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organization: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organization that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development. That’s our vision. We’re driven by it. And we need talented people who share it. If you’re as driven as we are, join us. You’ll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

Requirements

• Complete Bachelor's Degree
• Strong previous experience in a Clinical Research environment as a CTA, SSU, Site Activation, Remote Monitoring and as CRA.
• Strong Microsoft Tools knowledge
• Advanced English - Communication, Writing and Reading
• Brazil - Remote

Responsibilities

• Work with the Site Selection Lead to ensure knowledge of the goals, scope and requirements of the project (e.g. number of sites required/country, number of positive responses required etc.) and ensure that high quality results are delivered.
• Identify study investigators/ sites for potential study participation, both from the database and other potential sources such as local intelligence/internet etc.
• Ensure all newly identified sites are data based appropriately, checked for quality status and are fully processed.
• To contact and build relationships with study investigators/ sites and networks in assigned areas (e.g. region(s), countries I countries or therapeutic area) for the conduct of feasibility and potential study participation.
• To liaise with country managers to gather country specific evidence to support Site Selection, e.g. site list review, country specific profile of sites, standard of care.
• To ensure that all data collected, in the conduct of Site Selection or site related country feasibility, is fully documented and kept up to date in relevant systems to build knowledge and intelligence.
• To ensure appropriate procedures are followed, whether Sponsor specific or according to ICON SOPs, Site Selection RACI.
• Ensure appropriate follow up with sites on any inconsistencies in data provided for analysis and to chase outstanding feasibility data to ensure a complete data set.
• To contact investigators, local ICON employees and collect data to support country choice in the conduct of feasibility assessments.
• To become a country expert on the investigator profile, healthcare setting, standard of care to ensure the best sites are approached for projects.
• To liaise cross-functionally with other departments such as Study Start Up, CRA management to get local intelligence on sites and support local data collection.
• Be an expert on how to interact with sites and obtain relevant information to support Site Selection.
• Use knowledge and experience to build efficiency in the process and consistently deliver high quality investigators, sites, and other data to the Functional Lead for your projects.
• Ensure debarred Investigators are not included in feasibilities or for study participation.
• Ensure relevant parties, such as Site Selection lead, Feasibility Manager or Project Manager are aware of any Audit or Regulatory findings that may influence reasons for site selection.
• Ensure confidentiality is maintained or appropriate confidentiality agreements are in place prior to study discussions.
• Ensure all investigator feedback and status of contact with the site is tracked and data based appropriately, including reasons for site selection /de-selection.
• Support other team members, e.g. seconded CRAs, on how to get the best information from sites, act as a trainer and mentor to new staff within the group.
• Identify high performing sites and develop relationships with them as a single point of contact during site selection and ensure that key data collected from/related to these sites are maintained in ICON's systems.
• Deliver high quality standards and strive for excellence, act in a proactive, flexible and responsive manner to both internal and external customer needs.
• Establish good relationships internally and externally.
• To undertake other reasonably related duties as may be assigned from time to time.
• Recognize, exemplify and adhere to ICON's value, which centers around our commitment to People, Clients and Performance.
• To embrace and contribute to our culture of process improvement with a focus on accelerating concept to cure.
• Travel (approximately 10%) domestic and/or international, as required.
• Responsible for implementing the project-specific Site Selection strategy at the country level.

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level