Actalent
Clinical Research Coordinator (Part‑Time Contract)
Location: On‑site
Schedule: 20 hrs/week for 3 months, then 12–15 hrs/week for another 3 months (potential for extension)
About the Role Seeking an experienced Clinical Research Coordinator (CRC) to support clinical research trials for one of the leading healthcare providers in the U.S. This is a hands‑on role requiring strong organizational skills, attention to detail, and the ability to work independently while mentoring junior CRCs.
Key Responsibilities
Recruit and consent research participants.
Conduct telephone or in‑person interviews and screen for eligibility.
Perform participant follow‑up via phone, email, or mail.
Prepare, mail, and process questionnaires and study correspondence.
Track study participants using MS Excel.
Maintain accurate and detailed records and files.
Review, clean, and enter participant data into databases.
Assist with literature reviews for proposals and manuscripts.
Handle bookkeeping for study budgets (ordering supplies, processing payments, participant incentives).
Perform miscellaneous administrative tasks (labels, copying, faxing, meeting prep, note‑taking, transcribing audio files).
Required Qualifications
MUST HAVE 3+ years of on‑site patient‑facing Clinical Research Coordinator experience.
High school diploma or GED required.
Phlebotomy experience.
Job Type & Location This is a Contract position based out of Las Vegas, NV.
Pay and Benefits The pay range for this position is $30.00 – $45.00/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 Las Vegas, NV.
Application Deadline This position is anticipated to close on Jan 14, 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.
Equal Opportunity Statement 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.
Accommodation Request 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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Schedule: 20 hrs/week for 3 months, then 12–15 hrs/week for another 3 months (potential for extension)
About the Role Seeking an experienced Clinical Research Coordinator (CRC) to support clinical research trials for one of the leading healthcare providers in the U.S. This is a hands‑on role requiring strong organizational skills, attention to detail, and the ability to work independently while mentoring junior CRCs.
Key Responsibilities
Recruit and consent research participants.
Conduct telephone or in‑person interviews and screen for eligibility.
Perform participant follow‑up via phone, email, or mail.
Prepare, mail, and process questionnaires and study correspondence.
Track study participants using MS Excel.
Maintain accurate and detailed records and files.
Review, clean, and enter participant data into databases.
Assist with literature reviews for proposals and manuscripts.
Handle bookkeeping for study budgets (ordering supplies, processing payments, participant incentives).
Perform miscellaneous administrative tasks (labels, copying, faxing, meeting prep, note‑taking, transcribing audio files).
Required Qualifications
MUST HAVE 3+ years of on‑site patient‑facing Clinical Research Coordinator experience.
High school diploma or GED required.
Phlebotomy experience.
Job Type & Location This is a Contract position based out of Las Vegas, NV.
Pay and Benefits The pay range for this position is $30.00 – $45.00/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 Las Vegas, NV.
Application Deadline This position is anticipated to close on Jan 14, 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.
Equal Opportunity Statement 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.
Accommodation Request 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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