Actalent
Job Title: Clinical Research Coordinator - Part Time
Job Description
The Research Coordinator will play a crucial role in assisting with the operational aspects of research studies. This includes tasks related to participant recruitment, data collection and management, as well as reporting results. This position offers the opportunity to contribute to clinical research trials in collaboration with leading healthcare providers in the U.S.
Responsibilities
Recruit and consent research participants.
Conduct telephone or in-person interviews to screen for participant eligibility.
Perform follow-up with study participants via telephone, email, 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 payments and participant incentives.
Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.
Required Skills & Experience
High school diploma or General Education Development (GED).
3+ years of on-site hands‑on Clinical Research Coordinator experience.
Experience with chart review, patient recruitment, EDC, EMR, and clinical research.
Knowledge of Good Clinical Practice (GCP).
Phlebotomy skills.
Work Environment This position is based on‑site in a clinic environment. The initial commitment is for 20 hours per week for 3 months, followed by 12‑15 hours per week for another 3 months, with potential for extension. The role offers an engaging and supportive work environment, collaborating with one of the leading healthcare providers in the U.S.
Job Type & Location This is a Contract position based out of Las Vegas, NV.
Pay and Benefits
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 Las Vegas,NV.
Application Deadline This position is anticipated to close on Jan 16, 2026.
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.
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Responsibilities
Recruit and consent research participants.
Conduct telephone or in-person interviews to screen for participant eligibility.
Perform follow-up with study participants via telephone, email, 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 payments and participant incentives.
Perform miscellaneous administrative tasks such as typing labels, copying, faxing, meeting preparation, note-taking, and transcribing audio files.
Required Skills & Experience
High school diploma or General Education Development (GED).
3+ years of on-site hands‑on Clinical Research Coordinator experience.
Experience with chart review, patient recruitment, EDC, EMR, and clinical research.
Knowledge of Good Clinical Practice (GCP).
Phlebotomy skills.
Work Environment This position is based on‑site in a clinic environment. The initial commitment is for 20 hours per week for 3 months, followed by 12‑15 hours per week for another 3 months, with potential for extension. The role offers an engaging and supportive work environment, collaborating with one of the leading healthcare providers in the U.S.
Job Type & Location This is a Contract position based out of Las Vegas, NV.
Pay and Benefits
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 Las Vegas,NV.
Application Deadline This position is anticipated to close on Jan 16, 2026.
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.
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