Clinical Research Coordinator RN

What We Offer

RNs with experience working in Oncology OR Clinical Research!

This position offers hybrid work opportunities!

What You'll Do

• Sets up and performs routine clinical trial related activities.
• Collects, enters and summarizes clinical trial data.
• Maintain clinical and professional competency standards.
• Generates study specific source documents (paper and/or electronic).
• Collects blood samples, cultures, tissues and other samples for processing, shipping and or analysis.
• Assures drug and device accountability is up to date and available at all times.
• Works with Sr. team members to prepare for and attend sponsor and/or FDA audits.
• Develop knowledge to understand protocol feasibility.
• With leader or senior team member guidance, coordinates scheduling of pre-site, initiation, monitoring and closeout visits.

Qualifications

• Nursing Levels: Must have current or compact RN licensure in the state of North Carolina.
• Clinical Research Coordinator I RN: Minimum 1 year* of nursing or clinical research experience required.
• Clinical Research Coordinator II RN: Minimum 5 years* of clinical research experience required.
• Clinical Research Coordinator III RN: Minimum 10 years* of clinical research experience required.
• Clinical Research Coordinator IV RN: Minimum 15 years* of clinical research experience required.
• Certification in Clinical Research required.

Additional Skills

• Requires demonstrated knowledge of complex financial research concepts gained through education and experience.
• Works with a high degree of independence, using direction and independent judgement in the execution of tasks.
• Human relations and interpersonal skills necessary for interacting patients and team members.
• Attention to detail and accuracy necessary.
• Ability and willingness to work irregular hours as necessitated by research protocols.
• Excellent verbal and written communication skills.
• Excellent telephone diplomacy.
• Working knowledge of Information Systems and database management.
• Excellent analytical and time management skills.
• Self-motivated and able to work independently as well as a team.
• Ability to prioritize and problem-solving skills, with demonstrated competency in applying clinical knowledge to patient management.
• Able to meet multiple deadlines for concurrent projects.
• Knowledge and assessment skills to provide age appropriate care and protocol requirements.
• Good Clinical Practice (GCP), Human Subjects Training, and International Air Transportation Association (IATA) certification for shipping hazardous and biological substances.