Clinical Research Nurse Coordinator I - 6 Months Contract
Job Description
Job Description
ERA Health Research is a fast-growing clinical research company seeking a Clinical Research Nurse Coordinator I for a 6-month contract position covering a maternity leave at our Midland, TX location. This role may transition into a full-time position, depending on business needs, but conversion is not guaranteed.
The Clinical Research Nurse Coordinator I will play a vital role in the safe and effective execution of clinical research within the clinical site. This role blends direct patient care with protocol adherence, regulatory awareness, and collaborative teamwork. The ideal candidate demonstrates strong clinical acumen, attention to detail, and a commitment to research integrity and participant safety.
KEY RESPONSIBILITIES
- Direct Patient Involvement: Provide clinical support to patients participating in research protocols, including administering study-related procedures such as vital signs assessment, venipuncture, nasal swabs, and medication dispensing or tracking.
- Eligibility Assessment: Review medical records and assist in evaluating participants’ eligibility based on protocol-defined criteria.
- Informed Consent: Support or obtain informed consent from participants in accordance with ethical, regulatory, and site-specific procedures.
- Compliance & Quality: Ensure adherence to Good Clinical Practice (GCP), clinical trial protocols, institutional policies, and applicable regulatory requirements.
- Clinical Documentation: Maintain accurate and up-to-date clinical and research documentation to ensure data integrity and compliance.
- Patient Safety Monitoring: Identify, record, and promptly communicate adverse events or safety concerns to appropriate personnel.
- Interdisciplinary Collaboration: Communicate effectively with investigators, coordinators, sponsors, and site teams to support protocol objectives and timelines.
- Regulatory & IRB Support (Preferred): Assist with IRB submissions or regulatory documentation as needed.
EDUCATION & EXPERIENCE
PREFERRED
- Familiarity with regulatory documentation
- Experience supporting clinical trials a plus
- Knowledge of clinical data systems and electronic health records
- Understanding of protocol workflow and subject scheduling
REQUIRED
- Bachelor's degree in Nursing or related healthcare field
- Active RN license in good standing for Texas state
- Minimum of 1–2 years of clinical experience; experience in clinical research preferred
- Ability to perform standard clinical procedures with confidence and skill
- Strong interpersonal and communication skills, especially in a multidisciplinary setting
- Highly organized with attention to documentation, workflow, and patient care quality
OTHER DUTIES
In addition to the specific responsibilities outlined above, this role may perform other tasks or projects as assigned by a supervisor or manager. These additional duties will fall within the scope of the role and contribute to the overall success of the team.
COMPENSATION
$43.00/hourly - $45.00/hourly
EEO STATEMENT
ERA Health Research provides equal employment opportunities to all without regard to race, color, religion, sex (including sexual orientation or gender identity), national origin, age, disability, genetic information, or other protected status. Applicants and employees with disabilities may be entitled to reasonable accommodations under the terms of the Americans with Disabilities Act and certain state or local laws. A reasonable accommodation is an adjustment to our standard application and/or interview and/or employment process which will ensure an equal employment opportunity without imposing undue hardship on ERA Health Research. Please inform our team if you are requesting accommodation to complete any forms or otherwise participate in the application process or perform the essential functions of this role.