Clinical Research Nurse

POSITION PURPOSE

The Research Nurse supports clinical research projects by managing participant recruitment, overseeing the administration of clinical trials, collecting data, and ensuring adherence to study protocols. The position involves direct patient care, monitoring of research participants, and facilitating communication between the clinical team and research staff. The Research Nurse helps ensure compliance with regulatory standards and institutional guidelines for clinical studies.

DUTIES & RESPONSIBILITIES

• Clinical Trial Management:
• Administer medications, treatments, or interventions as per study protocol.
• Monitor participant reactions and any adverse events.
• Collect biological samples (blood, urine, etc.) or perform other necessary procedures.
• Document all trial-related procedures and observations accurately.
• Ensure participant safety and confidentiality at all times.
• Data Collection and Documentation:
• Record all patient information, research data, and observations in databases or case report forms.
• Maintain study records in compliance with Good Clinical Practice (GCP) and regulatory requirements.
• Prepare reports for review by the Principal Investigator or research team.
• Participant Follow-up:
• Schedule and monitor participant follow-up visits as per study protocol.
• Educate participants about the study’s goals, procedures, and any risks involved.
• Address participant questions or concerns regarding the study.
• Collaboration and Communication:
• Collaborate with the research team, including physicians, coordinators, and laboratory staff.
• Act as a liaison between patients and the research team.
• Assist in organizing study-related meetings and events.
• Regulatory Compliance and Quality Assurance:
• Adhere to ethical guidelines, regulatory requirements, and institutional policies for clinical research.
• Ensure compliance with Institutional Review Board (IRB) protocols and sponsor regulations.
• Monitor adverse events and report findings according to protocol guidelines.
• Training and Education:
• Stay updated on clinical trial protocols, ethical guidelines, and regulatory standards.
• Provide training to new staff or researchers regarding study procedures and safety protocols.

EDUCATION & EXPERIENCE

Qualifications:

• Education:
• Registered Nurse (RN) with a valid nursing license (required).
• Bachelor of Science in Nursing (BSN) preferred.
• Certification in Clinical Research (CCRC) or Clinical Research Nurse certification is a plus.
• Experience:
• Previous experience in clinical research, particularly in patient management, is highly preferred.
• Familiarity with clinical trial protocols, Good Clinical Practice (GCP), and regulatory guidelines.
• Skills:
• Strong clinical skills in patient care and assessment.
• Excellent communication skills to interact with participants, families, and research staff.
• Attention to detail, with the ability to record and manage data accurately.
• Ability to work independently and as part of a team in a fast-paced environment.
• Other Requirements:
• Knowledge of data management software and electronic medical records (EMR).
• Ability to handle sensitive information with discretion and maintain confidentiality.
• Ability to work flexible hours, including evenings or weekends, depending on the study.

Physical Requirements:

• May require travel to clinical sites or research locations.

Work Environment:

• Work may take place in in a clinical trial site
• Involves direct patient interaction and the potential for exposure to medical risks, such as bloodborne pathogens, while following safety protocols.

PHYSICAL/MENTAL DEMANDS: Must be able to stand for long periods of time as well as walking frequently. Exert up to 35 lbs. of force occasionally and/or up to 10 lbs. of force constantly to lift, carry, push, pull, or otherwise move objects, including the human body. Must be able to observe safe practice criteria in assisting patients and must be able to safely support the full weight of a patient when necessary. Mental demands consist of Supply Management, Verbal Communication, Professionalism, Customer Focus, Confidentiality, Bedside Manner, Medical Teamwork. Must be able to handle stressful situations. Must possess mental acuity for attention to accuracy and detail.

Job Type: Full-time

Pay: $50,000.00 - $65,000.00 per year

Benefits:

• 401(k)
• Dental insurance
• Health insurance
• Paid time off
• Vision insurance

Physical Setting:

• Clinic

Schedule:

• 8 hour shift
• Monday to Friday

Ability to Commute:

• San Antonio, TX 78218 (Preferred)

Ability to Relocate:

• San Antonio, TX 78218: Relocate before starting work (Preferred)

Work Location: In person

Salary : $50,000 - $65,000