Job Title: Clinical Research Nurse - Oncology Based (Must have onco exp)

Job Description

Join a prestigious academic research institute committed to pioneering scientific discoveries in basic, clinical, and population-based cancer research. As a Clinical Research Coordinator, you will play a vital role in reducing cancer incidence, mortality, and morbidity by facilitating high-profile studies and working with state-of-the-art equipment.

Responsibilities

• Screen and enroll subjects into clinical trials.
• Explain the informed consent process to participants.
• Document adverse events during the trial.
• Collect and manage study documents, including protocols, regulatory documents, informed consents, case report forms, and source documents.
• Prepare applications for the Institutional Review Board (IRB).

Essential Skills

• Registered Nurse with a license in the Commonwealth of Pennsylvania.
• Minimum of two to three years of clinical research experience.
• Experience in hematology and cancer medication administration.
• Proficiency in adverse event reporting using CTCAE 4.0.
• Effective communication and writing skills.
• Ability to multi-task and problem solve.
• Demonstrated teamwork and independent working capabilities.
• Knowledge of IRB and human research protection regulations.
• Strong computer skills, particularly in MS Office Suite.

Additional Skills & Qualifications

• Bachelor of Science in Nursing (BSN) preferred.
• Experience in oncology is highly advantageous.

Work Environment

The role is based in a fast-paced environment on a large campus, offering the opportunity to work with one of the most prestigious academic research institutes globally. You will be involved in high-profile studies with renowned sponsors, utilizing cutting-edge technology.