Clinical Research Infusion Nurse

Actalent Inc

Grand Rapids, MI

JOB DETAILS
SALARY
$35–$40 Per Hour
SKILLS
Adverse Events, Artificial Intelligence (AI), Candidate Screening, Centralized Operations/Management, Chemotherapy, Clinical Assessment, Clinical Nursing, Clinical Practices/Protocols, Clinical Research, Clinical Study Publications, Clinical Trial, Design Services, Documentation, Electrocardiogram, Electronic Medical Records, Emergency Medicine, Emergency Response, Environmental Monitoring, Genetics, Hospital, Intravenous Therapies, Nursing, Patient Education, Phlebotomy, Quality Management, Registered Nurse (RN), Regulations, Regulatory Compliance, Regulatory Requirements, Research Administration, Research Nursing, Research Protocols, Safety/Work Safety, Side Effects, Specimen Collection, Standard Operating Procedures (SOP), Technical/Engineering Design, Time Management
LOCATION
Grand Rapids, MI
POSTED
1 day ago

Job Title: Clinical Research Nurse

Job Description

This role provides specialized nursing care to participants enrolled in clinical trials, with a focus on chemotherapy, immunotherapy, and investigational agents. The Clinical Research Nurse administers study treatments, performs protocol-driven procedures, monitors participant safety, and ensures accurate documentation in compliance with applicable regulations and Standard Operating Procedures. This position plays a key role in supporting high-quality clinical research while prioritizing participant dignity, health, safety, and welfare.

Responsibilities

  • Administer chemotherapy, immunotherapy, and investigational agents, including parenteral therapies, in accordance with study protocols and applicable regulations.
  • Perform study-related clinical procedures such as venipuncture, obtaining blood specimens, peripheral IV insertion, and venous access device (central line) management.
  • Collect biological samples strictly following the study protocol and Standard Operating Procedures.
  • Perform ECG collection and obtain vital signs as required by the clinical trial protocol.
  • Use nursing assessment skills to monitor participants' general well-being and identify potential adverse events during and after study treatment.
  • Document clinical observations, adverse events, and all relevant data accurately and completely according to the protocol and Standard Operating Procedures.
  • Respond promptly and appropriately to emergency situations using established nursing standards and clinical judgment.
  • Educate, explain, and inform participants about study procedures, expectations, and their role in the clinical trial.
  • Provide patient education on chemotherapy, immunotherapy, and investigational agent administration, including potential side effects and symptom management.
  • Ensure that participant dignity, health, safety, and welfare remain the highest priority at all times throughout the course of the study.
  • Work effectively and efficiently under tight deadlines, managing high volumes of work and multiple interruptions while maintaining accuracy and quality.
  • Utilize electronic medical record (EMR) systems to document care, treatments, and study-related data in a timely and accurate manner.

Essential Skills

  • Active Registered Nurse (RN) licensure.
  • Experience starting peripheral IVs and managing central lines.
  • Proficiency in using electronic medical record (EMR) systems.
  • Ability to work effectively and efficiently under tight deadlines, high volumes, and multiple interruptions.
  • Strong nursing assessment skills for monitoring participant well-being and identifying adverse events.
  • Ability to respond to emergency situations based on nursing standards.

Work Environment

This position operates in a fast-paced clinical research setting that supports high volumes of participants and study activities. The role follows a daytime schedule, typically from 7:30 a.m. to 5:00 p.m., requiring consistent on-site presence during these hours. Nurses regularly use electronic medical record (EMR) systems and standard clinical equipment such as IV supplies, venous access devices, ECG machines, and vital sign monitors. The environment emphasizes strict adherence to study protocols, regulatory requirements, and Standard Operating Procedures while maintaining a professional, patient-centered atmosphere focused on safety, accuracy, and high-quality care.

Job Type & Location

This is a Contract position based out of Grand Rapids, MI.

Pay and Benefits

The pay range for this position is $35.00 - $40.00/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 Grand Rapids,MI.

Application Deadline

This position is anticipated to close on Jul 3, 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 20,000 consultants and 5,000 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.

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.

About the Company

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Actalent Inc