Onsite CRC II: Recruitment & Study Coordination

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

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.