Job Description

Job Description

Job Description

DAY SHIFT ONLY

Job Title: Clinical Research Technician

Job Description

The Clinical Research Technician supports the safe and accurate conduct of clinical trials by performing advanced technical procedures and direct participant care activities in a Phase I research setting. This role focuses on the safety, welfare, and comfort of study participants while ensuring all procedures follow study protocols, regulatory requirements, standard operating procedures (SOPs), scope of practice, and current training status. The technician assists with meal administration, sample collection and processing, vital signs, ECG procedures, dose verification, and documentation to maintain high-quality clinical research data and participant care.

Responsibilities

• Perform advanced technical procedures in support of clinical trials, including meal administration, subject positioning, bag checks, vital sign collection, ECG lead placement, phlebotomy, urine collection, PK runner duties, height/weight/BMI measurements, and dose verification, in alignment with protocol and current training.
• Administer study meals by ensuring the correct meal with the correct content is delivered to the correct study participant, following all protocol requirements and timing specifications.
• Conduct subject bag checks to ensure no contraband is present on the study floor and maintain a safe and compliant unit environment.
• Carry out study activities such as ECG positioning, supervised exercises, and other protocol-specific procedures that require monitoring and supervision of participants.
• Perform venipuncture, capillary, and/or IV specimen collection from study participants according to established protocols while maintaining strict aseptic technique.
• Manage biological samples accurately, including the collection, labeling, identification, transport, and processing of blood, urine, and other specimens to ensure sample integrity and chain of custody.
• Assist with dose verification by accurately confirming subject identity and dosing labels during dose administration, acting as an additional quality check to support protocol compliance.
• Promptly report any subject complaints or potential adverse events to charge staff or appropriate clinical personnel to ensure timely evaluation and treatment.
• Measure and record physical parameters, including height, weight, and BMI calculations, in accordance with protocol requirements.
• Obtain and document vital signs such as blood pressure, pulse oximetry, heart rate, temperature, and respiratory rate, ensuring accurate and timely data entry.
• Place ECG electrodes and leads accurately to enable precise telemetry monitoring and high-quality ECG data collection.
• Perform additional delegated clinical and research tasks as assigned and supervised by charge staff, within scope of practice and training.
• Review study-specific training materials and applicable protocols to develop a thorough understanding of study procedures as they relate to assigned responsibilities.
• Ensure that the Delegation of Authority and Training Logs for each study are completed accurately and in a timely manner.
• Stay current with and adhere to SOPs, Good Clinical Practice (GCP) and ICH guidelines, as well as relevant state and national laws and ethical standards governing clinical research.
• Observe and comply with all HIPAA, OSHA, Exposure Control, and Emergency Response regulations as required by applicable training.
• Create and maintain accurate, complete, and timely records of all protocol activities and events as delegated and trained, ensuring data quality and regulatory compliance.
• Monitor the progress of volunteers during study participation and provide for their care, comfort, and safety by attending to their needs and promptly addressing concerns.
• Participate in quality assurance activities related to clinical research projects and proactively identify and communicate opportunities for process improvement as they impact clinical practice.
• As required by study or site needs and if appropriately trained and delegated, perform additional procedures such as obtaining participant information and medical histories, administering questionnaires, coordinating meals, obtaining vital signs and EKGs, assisting with drug administration, collecting specimens, and conducting luggage or personal item searches.

Essential Skills

• Demonstrated experience performing venipuncture and phlebotomy safely and accurately in a clinical or research setting.
• Ability to perform clinical research procedures such as vital sign collection, ECG lead placement, and specimen collection according to protocol.
• Familiarity with the conduct of clinical trials and the practical activities required to support study protocols.
• Ability to follow detailed written protocols, SOPs, and regulatory requirements with strong attention to accuracy and compliance.
• Competence in maintaining aseptic technique during specimen collection and handling.
• Strong observational skills to monitor participant safety, identify potential adverse events, and escalate concerns appropriately.
• Effective documentation skills to create and maintain accurate records of protocol activities and events.
• Ability to work under supervision while carrying out delegated tasks responsibly and reliably.
• High school diploma or GED or higher level of education.
• Phlebotomy skills and training suitable for performing blood draws in a research environment.

Additional Skills & Qualifications

• Experience in a clinical research environment, particularly in clinical trials or Phase I studies, is beneficial.
• Experience in pre-screening patients or participants for clinical studies is advantageous.
• Knowledge of Good Clinical Practice (GCP) and ICH guidelines is highly desirable.
• Familiarity with HIPAA, OSHA, and Exposure Control regulations supports effective compliance.
• Ability to learn and apply new SOPs, protocols, and study-specific procedures quickly.
• Strong interpersonal and communication skills to interact professionally with study participants and clinical staff.
• Commitment to participant safety, comfort, and ethical standards in clinical research.
• Interest in professional growth within clinical research, with motivation to pursue advancement opportunities.

Work Environment

This position is based in a Phase I clinical research unit located in West Bend, Wisconsin. The environment is a structured, protocol-driven clinical setting focused on early-phase clinical trials and intensive participant monitoring. The role involves frequent direct interaction with study participants, hands-on clinical procedures, and collaboration with clinical and research staff. Work may include varied hours aligned with study schedules, dosing times, and sample collection windows. The unit operates under strict regulatory, safety, and privacy standards, including adherence to GCP, ICH, HIPAA, OSHA, and site-specific SOPs. The setting is professional and clinical, with appropriate attire required to support infection control, safety, and professional presentation while performing patient-facing and laboratory-related tasks.

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

The pay range for this position is $18.00 - $25.00/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)

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

This position is anticipated to close on May 22, 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 process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.

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.

Massachusetts Lie Detector: It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.

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.

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