Infusion Nurse

Posted 5 Hours Ago
Be an Early Applicant
Grand Rapids, MI, USA
In-Office
Mid level
Healthtech • Biotech • Pharmaceutical
The Role
Provide direct infusion nursing care for oncology clinical trial participants: administer chemotherapy/immunotherapy/investigational agents, perform venipuncture and IV/central line management, collect samples and vitals, educate patients on trials and side effects, coordinate protocol-related procedures, and document per SOPs and EHR.
Summary Generated by Built In

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access” to cutting edge trials throughout the United States and Europe.  

We are seeking an Infusion Nurse. The Infusion Nurse is responsible for providing direct patient care to individuals who are participants in research protocols that are conducted at START. The Infusion Nurse uses appropriate professional judgment and decision-making in planning and providing care. Nursing care is to be delivered in a manner consistent with the Standard Operating Procedures and standards of practice, and professional evidence-based standards.

Location: 5800 Foremost Dr SE, Grand Rapids, Michigan 49546

Patient Care

  • Administer chemotherapy/immunotherapy/investigational agent to participants (inclusive of parenteral) according to the protocol and applicable regulations.
  • Perform study-related activities including but not limited to venipuncture, obtaining blood specimens, IV insertion, and venous access device (central line) management, ECG collection, and vital signs.
  • Collect biological samples according to the protocol and Standard Operating Procedures.
  • Provide patient education regarding participation in a clinical trial, chemotherapy/immunotherapy/investigational agent administration and potential side effects.

Planning and problem-solving tasks 

  • Prepare for clinic day ensuring necessary supplies.
  • Assist with entry and completion of quality standards for EHR/PQRS.

Communicating tasks 

  • Communicate with providers regarding a change in patient status.

Protocol management tasks 

  • Work with study team to ensure that study related procedures, drug administration, labs, vital signs and ECG are completed. 

Education & Experience

  • High School Diploma or GED.
  • Licensed Registered Nurse in practicing state.
  • 2 - 4 years of experience in peripheral IV insertion and management of venous access device(s). 

Preferred Experience

  • Oncology Certified Nurse (OCN) certification.
  • Clinical Trial and oncology experience.
  • Experience working with Microsoft Office, including Teams, Excel and Word. 

Best-in-Class Benefits and Perks 

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:  

  • 401(k) retirement savings plan with employer match 
  • Eligibility for an annual performance bonus, based on role and company results 
  • Generous paid time off and paid holidays 
  • Comprehensive medical, dental, and vision coverage and optional insurance options 
  • Company paid life and disability insurance for added financial protection 
  • Employee Assistance Program (EAP) providing confidential, no‑cost support for you and your family from day one 
  • Flexible FSA and HSA plans to support your financial wellness 
  • Commitment to a supportive environment that values balance, wellbeing, and flexibility 
  • We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation. 

More About START 

START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”. 

Learn more at STARTresearch.com.  

Ready to be part of a team changing the future of cancer treatment? 

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law. 

Skills Required

  • High School Diploma or GED
  • Licensed Registered Nurse in practicing state
  • 2-4 years experience in peripheral IV insertion and management of venous access devices
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The Company
294 Employees
Year Founded: 2007

What We Do

Deeply rooted in community oncology centers globally, the START Center for Cancer Research ('START') provides patients with access to specialized Phase 1 clinical trials for novel anti-cancer agents. With research sites in the United States and in Spain, Portugal, and Ireland, START’s clinical trial sites have conducted more than 1,500 early phase clinical trials, including for 50 therapies that have gained FDA/EMA approval.

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