Clinical Research Coordinator 2

Accellacare; Knoxville (TN); On-site; USD 55,000 - 85,000; Full time

Benefits offered by this job

Health insurance

Annual leave

Retirement planning

Employee assistance program

Job summary

Accellacare, part of ICON's clinical research network, seeks a Clinical Research Coordinator 2 for our Knoxville, TN site. This onsite role focuses on recruiting participants, coordinating studies, and ensuring data quality per protocol.

You will manage start-up activities, screen participants, attend investigator meetings, and maintain documentation. Monitors and sponsor communications accompany EDC/CRF data entry responsibilities.

Qualifications

• Requires 2+ years of CRC experience.
• Bachelor's degree in life sciences or related field.
• Strong attention to detail and time management skills.

Responsibilities

• Perform study start-up duties including recruitment tools, progress notes, and on-site screening.
• Develop and execute recruitment plans to meet enrollment goals.
• Maintain training on the Clinical Trial Management System and update databases, reimburse participants, and create call lists.

Skills

Attention to detail

Time management

Career in clinical research

Education

Bachelor's degree in life sciences

Job description

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 site
• Proactively develops and executes recruitment plans that meet and exceed enrollment goals
• Performs 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 Guidelines
• Accurately collects study data via source documents/progress notes as required by the protocol
• Performs 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 protocol
• Performs 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 trials
• Documents 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 Investigator
• Maintains communication with the monitor from the sponsoring company through telephone contact, written communication and on-site visits
• Enters visit data in the Electronic Data Capture (EDC) or Case Report Forms (CRF) within timelines provided by sponsor

Your Profile

• 2+ years of experience as a Clinical Research Coordinator
• Strong attention to detail
• Motivated about a career in clinical research
• Excellent time management and planning skills with an organized approach to work
• Bachelor's degree in life sciences or other related field

What ICON Can Offer You

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our Benefits Examples Include

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

At ICON, inclusion & belonging are fundamental to our culture and values. 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.