Clinical Research Nurse

Clinical Research Nurse (Contract Position)

Contract Duration: Open ended contract

Job Type: Full-time 40 hours per week (Monday-Friday) - during normal business hours

Start Date: ASAP

Job Description

We are seeking a full-time, onsite Clinical Research Nurse (CRN) with experience in clinical research to support an ongoing Oncology clinical trial. The ideal candidate will be able to work independently and act as one of the main CRN's for this study. As the position and study progress, additional responsibilities may be assigned. The candidate must be flexible and willing to assist with various tasks as needed.

Key Responsibilities

Patient Recruitment: Identify and recruit suitable patients for the clinical trial.

Medical Record Review: Conduct thorough reviews of patient medical records.

Participant Screening: Perform phone screenings or prescreen participants for eligibility.

Informed Consent: Obtain informed consent from trial participants.

Data Management: Collect study data and enter it into electronic data capture (EDC) systems and address and resolve data queries promptly.

Medical Record Retrieval: Obtain necessary medical records for the study.

Documentation: Create and maintain source documents.

Compliance: Ensure compliance with e-diary protocols.

Regulatory Support: Assist with Institutional Review Board (IRB) approvals and provide regulatory support.

Adverse Event Reporting: Assist with timely reporting of adverse events (AEs) and serious adverse events (SAEs).

Study Visit Preparation: Organize participant schedules, ensure informed consent, prepare necessary documentation and coordinate with the research team to ensure all protocols are followed.

Specimen Collection and Processing: Obtain biological specimens from participants, label and temporarily store specimens, perform initial processing like serum separation and transport specimens to a lab for further analysis and storage.

Study Binder Maintenance: Keep study binders organized and up-to-date.

Participant Follow-Up: Conduct follow-up with study subjects to ensure retention.

Scheduling: Arrange in-patient visits and follow-up appointments and send reminders.

Administrative Tasks: Perform various administrative duties as required.

Phlebotomy: Perform phlebotomy.

Injections: Administer intermuscular, subcutaneous, or intradermal injections.

Sample Collection: Collect non-invasive samples (mouth swab, urine, sputum, etc.).

ECGs: Perform ECGs.

Vital Signs: Collect and record basic vital signs.

Product Dispensation: Dispense oral products.

Qualifications

• Minimum of two years of experience as a Clinical Research Nurse

• Registered Nurse (RN) license in FL

• IP administration experience

• Specific experience in Oncology clinical trials preferred

• Proficiency with electronic medical records (EMR) and electronic data capture (EDC) systems

Pay and Benefits

The pay range for this position is $35.00 - $45.00

• 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 Orlando,FL.

Application Deadline

This position will be accepting applications until Jan 21, 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.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

• Hiring diverse talent

• Maintaining an inclusive environment through persistent self-reflection

• Building a culture of care, engagement, and recognition with clear outcomes

• Ensuring growth opportunities for our people

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 ~~~ (~~~) for other accommodation options.