Actalent
Job Title: Clinical Research Coordinator
We are seeking a Clinical Research Coordinator to join our top‑ranked research team. In this role, you will work under the general direction of the Principal Investigator to ensure all protocols are conducted in accordance with Good Clinical Practice (GCP) principles. You will play a critical role in coordinating clinical research studies, ensuring compliance with regulations, and maintaining high ethical standards.
Key Responsibilities
Develop strong working relationships and maintain effective communication with study team members.
Coordinate day‑to‑day activities of research visits, including vital signs, EKG, phlebotomy, and lab work assessments.
Ensure subjects participating in clinical trials follow the study protocol as directed.
Maintain and organize study source documents; report adverse events promptly.
Ensure the safety of subjects during the study.
Educate subjects on protocols, study interventions, and study drugs.
Ensure data collected is accurate, legible, and organized according to GCP.
Qualifications
Clinical Research Coordinator experience (minimum 2 years).
Phlebotomy skills and experience with EKG and injections.
Proficiency in Good Clinical Practice (GCP).
Proficiency with MS Office suite (Outlook, Word, Excel, PowerPoint, SharePoint) and clinical trial master filing systems.
Understanding of study drug background and study requirements.
Job Type & Location Contract to Hire position based out of Omaha, NE.
Pay And Benefits The pay range for this position is $25.00 – $29.00/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:
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 Omaha, NE.
Application Deadline: This position is anticipated to close on Jan 12, 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.
Actalent 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.
#J-18808-Ljbffr
Key Responsibilities
Develop strong working relationships and maintain effective communication with study team members.
Coordinate day‑to‑day activities of research visits, including vital signs, EKG, phlebotomy, and lab work assessments.
Ensure subjects participating in clinical trials follow the study protocol as directed.
Maintain and organize study source documents; report adverse events promptly.
Ensure the safety of subjects during the study.
Educate subjects on protocols, study interventions, and study drugs.
Ensure data collected is accurate, legible, and organized according to GCP.
Qualifications
Clinical Research Coordinator experience (minimum 2 years).
Phlebotomy skills and experience with EKG and injections.
Proficiency in Good Clinical Practice (GCP).
Proficiency with MS Office suite (Outlook, Word, Excel, PowerPoint, SharePoint) and clinical trial master filing systems.
Understanding of study drug background and study requirements.
Job Type & Location Contract to Hire position based out of Omaha, NE.
Pay And Benefits The pay range for this position is $25.00 – $29.00/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:
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 Omaha, NE.
Application Deadline: This position is anticipated to close on Jan 12, 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.
Actalent 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.
#J-18808-Ljbffr