Job Description
We are seeking a diligent and detail-oriented Research Coordinator to assist with the operational tasks associated with implementing a research study. The role involves recruitment, data collection, data management, and reporting of results, contributing significantly to the success of our clinical research trials.
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, e-mail, 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).6+ months of clinical research experience.Experience in the medical field, phlebotomy, and vaccines.Additional Skills & Qualifications
Tech savvy.Interest in growing in Clinical Research.Proficient in data entry.Experience with chart review, patient recruitment, electronic data capture (EDC), and electronic medical records (EMR).Knowledge of Good Clinical Practice (GCP) guidelines.Work Environment
This position requires working five days on site. You will be supporting one of the leading healthcare providers in the US, offering a unique opportunity to be involved in clinical research trials. The work environment is collaborative and focused on advancing healthcare through research.
Job Type & Location
This is a Contract position based out of Bristol, Tennessee.
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 Bristol,TN.
Application Deadline
This position is anticipated to close on Sep 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.