Clinical Research Coordinator 2

Clinical Research Coordinator 2 - Knoxville, TN (Onsite)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.We have an incredible opportunity for ar 2 to join ICON’s Accellacare team. The CRC 2 ensures the safety of our volunteers, promotes the mission of Accellacare, and strives to meet and exceed study priorities. This individual is responsible for recruiting and promoting our service to suitable participants and sponsor representatives. Additionally, the CRC 2 will perform tasks required to coordinate and complete a study according to the protocol.This role is with Accellacare, part of ICON's clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.Location: 100% Onsite at Accellacare (1200 Merchant Drive, Knoxville, TN 37912)Hours: Monday – Friday; 8:00am – 5:00pm (no weekends or holidays)What you will be doing:Performs study start-up duties including the production of a recruitment tool, and progress notes, as well as phone screening patients and identifying participants for trials on siteProactively develops and executes recruitment plans that meet and exceed enrollment goalsPerforms study start-up duties including the production of a recruitment plan, recruitment tool, and progress notes, as well as phone screening participants.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. Attends investigator meetings Creates and updates source documents/progress notes and utilizes templates provided in the Core Operating GuidelinesAccurately collects study data via source documents/progress notes as required by the protocolPerforms technical requirements of the study protocol, i.e., lab work (phlebotomy and processing), blood pressure, electrocardiograms, Holtor 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 specified by a protocolPerforms continuous reviews of the inclusion and exclusion criteria for each participant during the trial for their trials as well as peer review of inclusion and exclusion for trialsDocuments laboratory data and adverse reactions, presents this information to an investigator in a timely manner, and immediately notifies investigators, the Institutional Review Board and sponsor of any serious adverse events Builds and maintains strong relationships with Investigators and provides ongoing communication about trial status and participants Dispenses study medication at the direction of the InvestigatorMaintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visitsEnters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsorYour Profile:2+ years of experience as a Clinical Research CoordinatorStrong attention to detailMotivated about a career in clinical researchExcellent time management and planning skills with an organized approach to workBachelor's degree in life sciences or other related field#LI-Office#LI-TP1#LI-AccellacareEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.Rewards & BenefitsICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.Benefits may include:Competitive base salary and performance related incentivesHealth and wellbeing programmes including medical, dental, and vision coverage where applicableRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities through structured training and career pathwaysBenefits may vary depending on role and location.Visit our careers site to read more about the benefits ICON offers.Inclusion and AccessibilityICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.Are you a current ICON Employee? Please click here to applySummaryLocation: US, Knoxville, TNType: Full time