Clinical Research Technician

Job Title: Clinical Research Technician

Job Description

We are seeking a dedicated Clinical Research Technician for our Phase I Clinical Research Unit. This role involves rotating through all three shifts, with minimal overnight duties due to our existing overnight staff. You will initially train on the first shift for 4-6 weeks. This position offers a dynamic schedule set 2-3 weeks in advance, including a weekend shift every other week. You will work closely with Clinical Research Nurses and Coordinators to manage Phase I Clinical Trials.

Responsibilities

• Accurately perform blood pressure, venipuncture, weights, pulse, respiratory rate, and temperature readings.

• Prepare and accurately record ECGs/Holters.

• Collect and process biological samples as specified in the protocol and ensure their proper distribution.

• Monitor meals to ensure dietary compliance by research participants.

• Assist in the preparation of rooms and medical equipment.

• Assist with screening procedures as needed.

• Maintain a clean, safe, and efficient working and study environment.

• Build respectful relationships with study participants.

• Accurately record all research data obtained or observed.

• Assist with quality control of source documents and case report forms.

• Maintain a basic understanding of current regulatory requirements.

• Attend all required meetings, as appropriate.

• Assist with study procedures as necessary.

• Maintain accurate records of all work undertaken.

• Maintain skills to perform all study tasks, as required.

• Ensure participant safety and dignity at all times.

• Handle participant complaints efficiently and effectively to maintain satisfaction.

• Ensure client and participant confidentiality is maintained.

• Respond to client and team queries in a timely manner.

• Take ownership of the quality and standard of own work.

Essential Skills

• Experience in patient care, laboratory work, and clinical research.

• Proficiency in EKG, clinical trials, sample preparation, phlebotomy, chart review, and understanding of biology.

• Knowledge of FDA, ICH, and GCP guidelines.

Additional Skills & Qualifications

• High School Diploma, CNA, Medical Assistant, EMT, or a BS Degree in Science/Healthcare.

• 0-2 years of experience in science, healthcare, or research.

• Phlebotomy skills are a plus.

Work Environment

This opportunity is based in our Phase I Clinical Research Unit in Madison, WI. Candidates will work in a state-of-the-art facility with access to advanced medical and research equipment. The work environment is professional, ensuring participant safety and confidentiality at all times. The role involves rotating shifts with varying start times, providing a diverse and hands-on experience in the clinical research field.

Job Type & Location

This is a Contract position based out of Madison, WI.

Pay and Benefits

The pay range for this position is $23.00 - $23.00/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 Madison,WI.

Application Deadline

This position is anticipated to close on Feb 6, 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@ (%20actalentaccommodation@) for other accommodation options.