Clinical Research Coord RN

Novant Health

60K–80K a year

Behavioral Health Market Context

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Job Description

esearch. If you are a dedicated and compassionate RN with a desire to make a difference in the healthcare industry, we encourage you to apply for this exciting opportunity.

Coordinate and manage all aspects of clinical trials and studies, including recruitment, enrollment, and scheduling of participants.
Ensure compliance with all regulatory and ethical standards set forth by governing bodies.
Work closely with physicians and other healthcare professionals to develop and implement research protocols.
Maintain accurate and detailed records of study data and participant information.
Communicate with study participants, providing necessary education and support throughout the research process.
Collaborate with the research team to analyze data and prepare reports for publication or presentation.
Monitor study progress and make necessary adjustments to ensure timely completion and accurate data collection.
Participate in the development and implementation of new research initiatives.
Stay current on industry advancements and changes in regulations related to clinical research.
Foster a positive and collaborative work environment to promote effective teamwork and communication.
Advocate for the importance of clinical research and its impact on patient outcomes.
Adhere to organizational policies and procedures to ensure the highest quality of care and ethical standards are met.

Novant Health is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.

Qualifications

  • The ideal candidate will possess strong communication and organizational skills, as well as a passion for improving patient outcomes through research

Benefits

    Responsibilities

    • In this role, you will play a crucial part in the advancement of medical research and treatment by coordinating various clinical trials and studies
    • Coordinate and manage all aspects of clinical trials and studies, including recruitment, enrollment, and scheduling of participants
    • Ensure compliance with all regulatory and ethical standards set forth by governing bodies
    • Work closely with physicians and other healthcare professionals to develop and implement research protocols
    • Maintain accurate and detailed records of study data and participant information
    • Communicate with study participants, providing necessary education and support throughout the research process
    • Collaborate with the research team to analyze data and prepare reports for publication or presentation
    • Monitor study progress and make necessary adjustments to ensure timely completion and accurate data collection
    • Participate in the development and implementation of new research initiatives
    • Stay current on industry advancements and changes in regulations related to clinical research
    • Foster a positive and collaborative work environment to promote effective teamwork and communication
    • Advocate for the importance of clinical research and its impact on patient outcomes
    • Adhere to organizational policies and procedures to ensure the highest quality of care and ethical standards are met


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