Clinical Research Nurse Coordinator I
$87,360–$97,760 year
On-siteMidland, Texas, United States
Job Summary
Coordinate clinical trials by identifying objectives, implementing protocols, and scheduling site initiation visits while ensuring adherence to GCP and IRB standards. Perform nursing assessments, administer investigational products, and conduct procedures such as vitals checks, ECGs, and IV starts. Manage study supplies, reconcile inventory, and complete pre-screening logs, informed consent, and randomization accurately. Assess and report adverse events, manage specimens, and coordinate patient visits with regulatory and clinical staff. Document data in EDC systems, resolve monitoring queries, and train new team members on clinical research skills. Travel to other company sites as needed to perform assigned duties.
Required Qualifications
- Active, unrestricted licensure as a Registered Nurse (RN) in the State of Texas
- At least one year clinical and/or clinical research experience
- Current CPR or Basic Life Support (BLS) certification, or the ability to obtain certification within the first 90 days of employment
- Venipuncture and IV start skills or ability to learn within first 30 days
- Meticulous attention to detail, with ability to follow complex instructions and protocols precisely
- Strong organizational and problem-solving skills
- Team player able to effectively self-reflect, communicate, and collaborate across teams
- Good written and verbal communication skills
- Proficient with basic computer software (MS Office)
- Travel to and from other company sites as needed to perform job responsibilities
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