Clinical Research Nurse I

IRE • San Antonio, TX

4d • Onsite

About The Position

ICON is a global healthcare intelligence and clinical research organisation focused on helping bring new medicines and treatments to patients faster. The Clinical Research Nurse I supports clinical research operations and the execution of clinical trials, following study protocols and providing compassionate patient care throughout the research process. This is a PRN/as-needed role based 100% onsite in San Antonio, Texas. The stated schedule is Monday through Friday, 6:00 AM to 2:30 PM.

The nurse assists with planning, implementing, and coordinating research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures. The role involves assessing patients, administering study treatments, performing protocol-required procedures, maintaining patient safety and ethical standards, documenting study data, collaborating with research teams, and educating participants and their families about study procedures, treatment regimens, and informed consent.

Requirements

• Bachelor's degree in Nursing (BSN) from an accredited institution.
• Current Registered Nurse (RN) licensure in the applicable jurisdiction.
• Minimum of 1–2 years of clinical nursing experience; research or academic healthcare experience and exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines are preferred.
• Strong clinical assessment and critical thinking skills, including the ability to recognize and respond to changes in patient status and communicate effectively with healthcare professionals and study investigators.
• Knowledge of clinical research regulatory requirements, including International Council for Harmonisation (ICH) guidelines and local requirements, and commitment to ethical standards and patient confidentiality.
• Proficiency with electronic medical record (EMR) systems, clinical documentation, and data entry, with attention to detail and accuracy.
• Excellent interpersonal and organizational skills and ability to work independently and collaboratively in a fast-paced, multidisciplinary environment, prioritize competing demands, and meet project deadlines.
• Must have the legal right to work in the country where the role is based.

Nice To Haves

• Clinical nursing experience in a research or academic healthcare setting.
• Exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.

Responsibilities

• Assist in planning, implementing, and coordinating clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures.
• Conduct patient assessments, administer study treatments, and perform clinical procedures required by the research protocol while ensuring patient safety and compliance with ethical standards.
• Collect, record, and maintain accurate and complete documentation, including medical histories, vital signs, adverse events, and laboratory results, in electronic case report forms and study databases.
• Collaborate with investigators, study coordinators, regulatory staff, and other multidisciplinary team members to support efficient study conduct, participant recruitment, and retention.
• Educate and counsel study participants and their families about study procedures, treatment regimens, and informed consent, and address questions or concerns.

Benefits

• Competitive base salary and performance-related incentives.
• Health and wellbeing programmes, including medical, dental, and vision coverage where applicable.
• Retirement and pension plans.
• Life assurance and disability coverage.
• Employee assistance programmes and wellbeing resources.
• Learning and development opportunities through structured training and career pathways.

What This Job Offers

• Career Level: Entry Level