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Clinical Research Nurse Specialist

2 months ago

Philadelphia, Pennsylvania, United States Actalent Full time
Job Summary

Actalent is seeking a highly skilled Clinical Research Nurse to join our team. As a Clinical Research Nurse, you will play a critical role in the success of our clinical trials by ensuring the highest level of quality and integrity in all aspects of research.

Key Responsibilities:
  • Screen and enroll subjects into clinical trials
  • Explain the informed consent process to participants
  • Document adverse events and collect study documents, protocols, regulatory documents, informed consents, case report forms, and source documents
  • Prepare Institutional Review Board (IRB) applications
  • Recruit, screen, and enroll subjects into clinical trials
  • Explain the informed consent process to participants
  • Document adverse events
  • Collect study documents, protocols, regulatory documents, informed consents, case report forms, and source documents
  • Prepare IRB applications
Requirements:
  • Registered Nurse with license in Commonwealth of Pennsylvania
  • BSN preferred
  • Minimum of two to three years clinical research experience required
  • Hematology experience preferred
  • Experience with cancer medications and adverse event reporting using CTCAE 4.0 preferred
  • Effective communication and writing skills
  • Ability to multi-task and problem solve
  • Demonstrated ability to work as part of a team as well as independently
  • Knowledge of IRB and human research protection regulations
  • Strong computer skills
Preferred Skills:
  • Clinical research
  • Research coordinator
  • Study coordinator
  • CRC
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.