Nurse Research Specialist
2 days ago
Clinical Research Nurse I is a highly skilled professional responsible for assisting in the planning, implementation, and coordination of clinical research activities. The ideal candidate will possess 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.
Key Responsibilities:
- Assist in the development and implementation of clinical research protocols, ensuring compliance with regulatory guidelines and standard operating procedures (SOPs).
- Conduct thorough patient assessments, administer study treatments, and perform clinical procedures as required by the research protocol, while prioritizing patient safety and 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 (eCRFs) 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, addressing any questions or concerns that may arise during the study.
Requirements:
- A 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 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.
- Familiarity with regulatory requirements governing clinical research, including the International Council for Harmonisation (ICH) guidelines, 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.
About ICON:
We offer a competitive salary of approximately $80,000 per year, various annual leave entitlements, a range of health insurance offerings, competitive retirement planning options, a Global Employee Assistance Programme (EAP), life assurance, and flexible country-specific optional benefits.
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