Actalent
Job Title
Clinical Research Nurse
Responsibilities
Collaborate with the Protocol Activation office to initiate and activate clinical trial protocols using the study start‑up task list.
Prepare and review study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.
Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals before study activation.
Review protocols, collect feedback, and resolve obstacles in collaboration with the Principal Investigator (PI).
Provide nursing education to other disciplines to ensure safe and effective care of enrolled patients.
Translate protocol treatment plans into sample orders.
Collaborate with the clinical research team to prescreen potential subjects and active cancer patients for clinical trials.
Review patient charts and medical history to confirm protocol eligibility.
Ensure the informed consent process is completed and documented according to IRB, GCP, and institutional policies.
Register consented research patients with study sponsors and enter data into the clinical trials database.
Serve as a link between patients and the research team, addressing challenges with protocol completion.
Ensure protocol‑specific orders are executed accurately, coordinating continuity of care between disciplines and sites.
Manage patient reimbursement while on clinical trials and deliver high‑quality oncology nursing care.
Grade adverse events and document toxicities according to protocol guidelines.
Complete Serious/Unexpected Adverse Event (SAE) forms and collaborate on overall protocol compliance.
Assist with bio‑specimen collection and processing, monitoring visits, audits, and database queries.
Maintain research records for screened and enrolled patients.
Provide training and orientation to other faculty and staff.
Ensure adherence to all regulations and guidelines throughout the research project.
Essential Skills
Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.
Bachelor’s Degree in Nursing preferred.
One year of oncology experience required.
Three to five years of oncology research experience preferred.
Maintains active Basic Life Support (BLS) certification.
Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.
Certification as a Clinical Research Professional (CCRP) preferred.
Detail‑oriented with excellent organizational skills.
Proficient in computer applications (the person™, Word, Excel, etc.).
Excellent communication and interpersonal skills.
Ability to maximize resources and be resourceful.
Additional Skills & Qualifications
Experience with clinical research coordination, patient recruitment, and enrollment.
Understanding of FDA, IRB, and GCP regulations.
Experience in teaching and training clinical staff.
Job Type & Location Contract to Hire, Somerville, New Jersey
Pay & Benefits Hourly pay: $55.00 – $57.00 per hour.
Benefits (subject to eligibility and classification):
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)
Application Deadline October 28, 2025
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.
For reasonable accommodations, please e‑mail
actalentaccommodation@actalentservices.com
for other accommodation options.
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Responsibilities
Collaborate with the Protocol Activation office to initiate and activate clinical trial protocols using the study start‑up task list.
Prepare and review study tools such as study binders, medication diaries, eligibility checklists, and flow sheets.
Verify Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals before study activation.
Review protocols, collect feedback, and resolve obstacles in collaboration with the Principal Investigator (PI).
Provide nursing education to other disciplines to ensure safe and effective care of enrolled patients.
Translate protocol treatment plans into sample orders.
Collaborate with the clinical research team to prescreen potential subjects and active cancer patients for clinical trials.
Review patient charts and medical history to confirm protocol eligibility.
Ensure the informed consent process is completed and documented according to IRB, GCP, and institutional policies.
Register consented research patients with study sponsors and enter data into the clinical trials database.
Serve as a link between patients and the research team, addressing challenges with protocol completion.
Ensure protocol‑specific orders are executed accurately, coordinating continuity of care between disciplines and sites.
Manage patient reimbursement while on clinical trials and deliver high‑quality oncology nursing care.
Grade adverse events and document toxicities according to protocol guidelines.
Complete Serious/Unexpected Adverse Event (SAE) forms and collaborate on overall protocol compliance.
Assist with bio‑specimen collection and processing, monitoring visits, audits, and database queries.
Maintain research records for screened and enrolled patients.
Provide training and orientation to other faculty and staff.
Ensure adherence to all regulations and guidelines throughout the research project.
Essential Skills
Graduate of an accredited school of nursing with a license to practice in the State of New Jersey.
Bachelor’s Degree in Nursing preferred.
One year of oncology experience required.
Three to five years of oncology research experience preferred.
Maintains active Basic Life Support (BLS) certification.
Oncology Nursing Society (ONS) certification as an Oncology Certified Nurse (OCN) or Advanced Oncology Certified Nurse (AOCN) preferred.
Certification as a Clinical Research Professional (CCRP) preferred.
Detail‑oriented with excellent organizational skills.
Proficient in computer applications (the person™, Word, Excel, etc.).
Excellent communication and interpersonal skills.
Ability to maximize resources and be resourceful.
Additional Skills & Qualifications
Experience with clinical research coordination, patient recruitment, and enrollment.
Understanding of FDA, IRB, and GCP regulations.
Experience in teaching and training clinical staff.
Job Type & Location Contract to Hire, Somerville, New Jersey
Pay & Benefits Hourly pay: $55.00 – $57.00 per hour.
Benefits (subject to eligibility and classification):
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)
Application Deadline October 28, 2025
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.
For reasonable accommodations, please e‑mail
actalentaccommodation@actalentservices.com
for other accommodation options.
#J-18808-Ljbffr