Clinical Research Nurse I

ICON plc • San Antonio, TX

1d • Onsite

About The Position

The Clinical Research Nurse I delivers clinical research operations work, supporting the execution of clinical trials while ensuring adherence to study protocols and providing compassionate patient care throughout the research process. This is an as-needed (PRN) position 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 clinical research activities in accordance with study protocols, regulatory guidelines, and standard operating procedures. The role includes conducting patient assessments, administering study treatments, performing protocol-required procedures, and maintaining patient safety and ethical standards. The nurse also collects and maintains accurate study documentation and data, collaborates with multidisciplinary research teams, and educates and counsels participants and their families about study procedures, treatment regimens, and informed consent.

Employment with ICON is contingent on having the legal right to work in the country where the role is based. ICON describes itself as a global healthcare intelligence and clinical research organisation whose mission is to bring new medicines and treatments to patients faster. Its stated values include integrity, collaboration, agility, and inclusion.

Requirements

• Bachelor's degree in Nursing (BSN) from an accredited institution.
• Current licensure as a Registered Nurse (RN) in the applicable jurisdiction.
• Minimum of 1–2 years of clinical nursing experience; research or academic healthcare experience is preferred, along with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines.
• 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 regulatory 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.
• 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 (SOPs).
• Conduct patient assessments, administer study treatments, and perform clinical procedures required by research protocols 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 (eCRFs) 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 regarding study procedures, treatment regimens, and informed consent, and address questions or concerns.

Benefits

• Competitive base salary and performance-related incentives.
• 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.
• Health and wellbeing programmes.

What This Job Offers

• Career Level: Entry Level