Clinical Research Nurse
1 day ago
We are seeking a highly skilled Clinical Research Nurse to join our team at ICON Clinical Research. As a Clinical Research Nurse, you will play a critical role in conducting clinical trials, ensuring patient safety and protocol adherence, and contributing to the advancement of innovative treatments and therapies.
Key Responsibilities:- Assist in the planning, implementation, and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures.
- Conduct patient assessments, administer study treatments, and perform clinical procedures as required by the research protocol, while ensuring patient safety and compliance with ethical standards.
- Collect, record, and maintain accurate and complete data documentation, including medical histories, vital signs, adverse events, and laboratory results, in electronic case report forms and study databases.
- Collaborate with multidisciplinary teams, including investigators, study coordinators, and regulatory staff, to ensure efficient study conduct, participant recruitment, and retention throughout the duration of the trial.
- Provide education and counseling to study participants and their families regarding study procedures, treatment regimens, and informed consent, while addressing any questions or concerns that may arise during the course of the study.
- Bachelor's degree in Nursing (BSN) from an accredited institution, with current licensure as a Registered Nurse (RN) in the applicable jurisdiction.
- Minimum of 1-2 years of clinical nursing experience, preferably in a research or academic healthcare setting, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.
- Strong clinical assessment and critical thinking skills, with the ability to recognize and respond to changes in patient status and communicate effectively with healthcare professionals and study investigators.
- Knowledge of regulatory requirements governing clinical research, including the International Council for Harmonisation (ICH) guidelines and local regulatory requirements, with a commitment to upholding ethical standards and patient confidentiality.
- Proficiency in electronic medical record (EMR) systems, clinical documentation, and data entry, with a high level of attention to detail and accuracy in recording patient information and study data.
- Excellent interpersonal and organizational skills, with the ability to work independently and collaboratively in a fast-paced, multidisciplinary environment, while prioritizing competing demands and meeting project deadlines.
- Competitive salary and benefits package.
- Opportunities for professional growth and development.
- A diverse and inclusive work environment.
- Recognition and rewards for outstanding performance.
At ICON Clinical Research, we are committed to providing a workplace free of discrimination and harassment. We are an equal opportunity employer and welcome applications from diverse candidates. If you need a reasonable accommodation for any part of the application process, please let us know or submit a request here. We look forward to hearing from you
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