Job Title: Clinical Research Coordinator

Job Description

The Research Coordinator will assist an Investigator, Research Associate, or Project Manager in operationalizing tasks associated with implementing a research study. This includes a variety of tasks related to recruitment, data collection, data management, and reporting of results.

Responsibilities

• Recruit and consent research participants.
• Conduct telephone or in-person interviews with participants, including screening for eligibility.
• Perform follow-up with study participants via telephone, email, and/or mail.
• Prepare, mail, and process questionnaires and other study correspondence.
• Assist in tracking study participants using MS Excel.
• Maintain accurate and detailed records and files of work.
• Review, edit, clean, and enter participant data into a database.
• Assist with literature reviews for proposal submissions and manuscript preparation.
• Manage bookkeeping related to study budgets, including ordering supplies and requesting checks for payment and participant incentives.
• Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.

Essential Skills

• High school diploma or General Education Development (GED).
• Experience in chart review, patient recruitment, electronic data capture (EDC), electronic medical records (EMR), and clinical research.
• Familiarity with Good Clinical Practice (GCP) guidelines.
• Strong customer service experience.
• Proficiency in navigating Excel and other Microsoft programs.
• Background in the medical field.

Additional Skills & Qualifications

• Tech-savvy with a keen interest in growing in the field of Clinical Research.
• Experience in data entry.

Work Environment

The position requires working on-site five days a week. This role offers an opportunity to work in Clinical Research Trials, supporting one of the leading healthcare providers in the US.

Pay and Benefits

The pay range for this position is $25.00 - $30.00/hr.

Eligibility requirements apply to some benefits and may depend on your job
classification and length of employment. Benefits are subject to change and may be
subject to specific elections, plan, or program terms. If eligible, the benefits
available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Knoxville,TN.

Application Deadline

This position is anticipated to close on May 18, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.