
Clinical Research Feasibility Coordinator
Posted Sep 15

Posted Sep 15
This is a fully remote position, open to applicants in Florida.
• Execute clinical research feasibility analyses for all sites in accordance with sponsor/CRO timelines and requirements.
• Evaluate protocols or protocol summaries and study specifics to carry out feasibility assessments.
• Collaborate with the Business Development team to pinpoint potential investigators and site leaders.
• Reach out to investigators and site leaders to discuss study particulars and evaluate study feasibility.
• Maintain a record of site capabilities and equipment, including MRI, PET, and CSF functionalities.
• Organize completed questionnaires and pertinent documents within the CRM.
• Submit and revise feasibility questionnaires as necessary.
• Input per-patient budget figures into relevant systems.
• Enter principal investigator details into sponsor, CRO, and related databases.
• Support the completion and collection of signatures for confidential agreements.
• Assist in managing the upcoming research trials pipeline and applications for new studies.
• Participate in company training, webinars, and mandatory meetings.
• Engage and collaborate with clients and internal/external stakeholders in a professional and timely manner.
• Uphold the confidentiality of patient, customer, and company information.
• Carry out other assigned responsibilities.
• A high school diploma or equivalent AND at least 2 years of administrative, sales support, or related experience, OR a comparable combination of education and experience is required.
• A minimum of 1 year of experience in clinical research is required.
• Previous experience with the feasibility process in a clinical research environment is strongly preferred.
• Bilingual proficiency in English and Spanish is advantageous.
• Proficient in Microsoft applications, email, electronic health records, web applications, and capable of typing at 40+ wpm.
• Ability to perform basic clinical tasks such as measuring blood pressure, taking vitals, conducting EKGs, and performing phlebotomy.
• Exceptional organizational skills and attention to detail.
• Strong written and verbal communication abilities.
• Well-honed interpersonal and listening skills; capability to work independently as well as with colleagues, subjects, managers, and external clients.
• Competence in effectively managing multiple tasks and adapting to shifting workloads and priorities.
• Professional demeanor, respect for others, self-motivation, and a robust work ethic.
• High level of integrity and reliability.
• Ability to work with minimal supervision, identify issues, and implement solutions.
• Capacity to manage highly sensitive information with confidentiality and professionalism, adhering to HIPAA guidelines.
• Full-time employees scheduled to work at least 30 hours per week are eligible for benefits, with coverage commencing on the first day of the month following the date of hire.
• Offered benefits include medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match.
Thermo Fisher Scientific
ICON plc
ICON plc
Clinical Outcomes Solutions
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