For a career opportunity with Accellacare, a division of one of the largest global Clinical Research Organizations in ICON Plc, please consider applying to our Clinical Research Coordinator opening. Job Summary: The CRC I reports directly to the Clinical Operations Manager, with the primary aim to coordinate multiple studies according to the study protocol, perform collection of clinical data points and to provide a seamless, customer service to the patients attending site.

Duties:

• Assisting Clinical Research Coordinators with patient visits, documentation, CRF completion, data queries and monitor visits.
• Performing technical requirements of study protocols, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, monitoring, pulmonary function testing, allergy testing, urine/serum pregnancy testing, strep throat screening, or any procedure necessary for the protocol as ordered by the investigator or coordinator.
• Assisting in the laboratory or with other laboratory duties such as performing quality assurance review, restocking of supplies and processing of specimens.
• Performing consult visits as needed.
• Completes training on Clinical Trial Management System and maintains proper skills to update database, complete participant reimbursement, capture referral source of participants, and create calls lists to promote recruitment.
• Assisting the Clinical Research Coordinator or other staff members with creating and copying patient files for study closeout procedures.
• Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor.
• Addresses all queries or data clarifications within 48 hours of receipt.
• Typing memos, letters, recruitment tools, progress notes and various documents.
• Filing labs and correspondence.
• Performing various errands to pick up dry ice, supplies, samples, physician signatures and storage boxes, etc.
• Assisting Clinical Research Coordinators or other staff members as determined by the needs and priorities of the research organization, and as time and abilities permit.
• Assisting with answering the telephones, making appointment reminder calls and initial phone screening.
• Travel to other sites within the network may be required to support increases in workload and, or studies/projects as needed.

Successful applicants will have the following:

• Bachelor's degree, or relevant industry-field training or experience
• High level of attention to detail
• Personable, able to build rapport with patients with ease
• Motivated about a career in clinical research
• Excellent planner, organized approach to work

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.

https://careers.iconplc.com/reasonable-accommodations