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Job Title: Clinical Research Coordinator

We are seeking a Clinical Research Coordinator to join our top-ranked research team. You will work under the general direction of the Principal Investigator to ensure that all protocols are conducted in accordance with Good Clinical Practice principles. You will play a key role in coordinating clinical research studies, ensuring compliance with regulations, and maintaining high ethical standards.

Responsibilities

+ Develop strong working relationships and maintain effective communication with study team members.

+ Coordinate the day-to-day activities of research visits, including vital signs, EKG, and lab work assessments.

+ Ensure that subjects participating in clinical trials follow the study protocol as directed.

+ Maintain and organize study source documents and report adverse events promptly.

+ Ensure the safety of subjects during the study.

+ Educate subjects on protocols, study interventions, and study drugs.

+ Ensure that data collected is accurate, legible, and organized according to good clinical practices.

Essential Skills

+ Proficiency in Good Clinical Practice (GCP).

+ Logical thinking and ability to prioritize tasks.

+ Strong interpersonal and team-building skills.

+ Ability to adapt quickly to changing business conditions.

+ Experience with EKG, phlebotomy, and injections.

Additional Skills & Qualifications

+ Minimum of 2 years of experience in healthcare.

+ Strong attention to detail and interpersonal skills.

+ Proficiency with MS Office suite (Outlook, Word, Excel, PowerPoint, SharePoint) and clinical trial master filing systems.

+ Ability to travel for study activities and attend meetings as required.

+ Understanding of study drug background and study requirements.

+ Friendly and outgoing demeanor with a passion for patient interaction.

+ Capability to lift 15 pounds occasionally and prolonged periods of desk work.

+ Ability to communicate effectively and work collaboratively in a multi-disciplinary team.

Job Type & Location

This is a 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 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 OMAHA,NE.

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 [email protected] (%[email protected]) for other accommodation options.