Clinical Research Technician

Clinical Research Technician

The Clinical Research Technician supports the safe and accurate conduct of clinical trials by performing advanced technical procedures and practical study activities in a Phase I research setting. This role focuses on protecting the safety and welfare of study participants while carrying out protocol-specific tasks in accordance with regulatory requirements, standard operating procedures, scope of practice, and current training. The technician works under supervision to perform clinical procedures, manage biological samples, document study activities, and maintain compliance with Good Clinical Practice and applicable guidelines.

Responsibilities

• Perform advanced technical procedures in support of clinical trials, including meal administration, subject positioning, bag checks, vital sign measurements, ECG lead placement, phlebotomy, urine collection, PK running, height, weight and BMI measurements, and dose verification.
• Administer study meals, ensuring the correct meal and content are delivered to the correct study participant according to protocol requirements.
• Conduct subject bag checks to ensure no contraband is present on the study floor and maintain a safe and compliant environment.
• Perform study activities such as ECG positioning, supervised exercises, and other protocol-defined procedures requiring direct supervision of subjects.
• Collect venous, capillary, and/or IV blood specimens from study participants using aseptic technique and in accordance with established protocols.
• Perform proper and accurate sample management, including collection, identification, transport, and processing of biological samples such as blood and urine.
• Assist with dose verification during dose administration by accurately verifying subject identity and dosing labels as an additional quality control step.
• Report any subject complaints or potential adverse events immediately to charge staff or appropriate clinical personnel to ensure timely evaluation and treatment.
• Measure and document physical parameters including height, weight, and BMI, ensuring accurate and consistent data collection.
• Measure and record vital signs, including blood pressure, pulse oximetry, heart rate, temperature, and respirations, in accordance with study protocols.
• Place ECG electrodes and leads accurately to support precise telemetry monitoring and high-quality ECG data collection.
• Perform additional delegated tasks from the study task list as assigned and supervised by charge staff.
• Review study-specific training materials and applicable protocols to develop a thorough understanding of study procedures relevant to assigned responsibilities.
• Ensure Delegation of Authority and Training Logs for each study are completed accurately and in a timely manner.
• Stay current with standard operating procedures, Good Clinical Practice (GCP), ICH guidelines, and applicable state and national laws and ethical standards.
• Observe and maintain compliance with HIPAA, OSHA, exposure control regulations, and emergency response procedures as required by training.
• Create and maintain accurate, complete, and timely records of all protocol activities and events as delegated and trained.
• Monitor the progress of volunteers during study participation and provide for their care, comfort, and safety by attending to their needs.
• Participate in quality assurance activities related to clinical research projects and proactively identify areas where quality improvements may be needed.
• As required by study or site needs and if appropriately trained and delegated, perform additional study procedures such as obtaining participant information and histories, administering questionnaires, handling meals, collecting vital signs and EKGs, assisting with drug administration, collecting specimens, and conducting luggage or bag searches.

Essential Skills

• Ability to perform advanced technical procedures in a clinical research environment, including meal administration, subject positioning, bag checks, vital signs, ECG lead placement, phlebotomy, urine collection, PK running, and physical measurements.
• Proficiency in venipuncture, capillary, and/or IV blood collection using aseptic technique and in accordance with established protocols.
• Competence in collecting, identifying, transporting, and processing biological samples such as blood and urine with high accuracy and attention to detail.
• Skill in accurate dose verification and subject identity confirmation during dose administration as part of quality control processes.
• Ability to measure and document height, weight, BMI, and a full range of vital signs, including blood pressure, pulse oximetry, heart rate, temperature, and respirations.
• Capability to place ECG electrodes and leads correctly to ensure accurate telemetry and ECG monitoring.
• Strong documentation skills with the ability to create and maintain accurate records of protocol activities and study events.
• Working knowledge of Good Clinical Practice (GCP), ICH guidelines, and adherence to relevant regulatory and ethical standards.
• Understanding of and compliance with HIPAA, OSHA, exposure control regulations, and emergency response procedures.
• Attention to participant safety, comfort, and welfare throughout study participation.
• Ability to follow detailed study protocols, standard operating procedures, and delegated task lists under supervision.
• High school diploma or GED or higher level of education.

Additional Skills & Qualifications

• Experience with quality control activities in a clinical or research setting, including identifying and supporting quality assurance initiatives.
• Familiarity with pre-screening patients or volunteers for clinical research participation.
• Experience with chart review and documentation in a clinical or research environment.
• Exposure to or experience in clinical research settings, particularly Phase I units, is beneficial.
• Ability to review and complete Delegation of Authority and Training Logs accurately and on time.
• Strong interpersonal skills to interact professionally with study participants and research staff.
• Ability to adapt to changing study needs and perform additional procedures when appropriately trained and delegated.

Work Environment

This position is based in a Phase I clinical research unit located in West Bend, WI. The work environment involves direct interaction with study participants in a controlled clinical setting where strict adherence to protocols, safety procedures, and regulatory standards is required. The role includes frequent handling of biological samples, use of clinical equipment such as blood pressure monitors, ECG machines, and telemetry systems, and participation in emergency response procedures as trained. Staff work closely with clinical and research teams in a structured environment focused on participant safety, data accuracy, and regulatory compliance.

Job Type & Location

This is a Permanent position based out of West Bend, WI.

Pay and Benefits

The pay range for this position is $45760.00 - $49920.00/yr.

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Workplace Type

This is a fully onsite position in West Bend, WI.

Application Deadline

This position is anticipated to close on Jun 11, 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.

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San Francisco Fair Chance Ordinance: Pursuant to the San Francisco Fair Chance Ordinance, for all positions located in the city and county of San Francisco, we will consider for employment qualified applicants with arrest and conviction records.

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Use of Artificial Intelligence (AI): We may use Artificial Intelligence (AI) to support parts of our hiring process, including sourcing, screening, and evaluating candidates. AI helps assess applications and qualifications, but final decisions are made by our hiring team. By applying, you acknowledge and agree that your application may be reviewed using AI tools.