What are the responsibilities and job description for the Clinical Research Coordinator position at Hoag Hospital Irvine?
CLINICAL RESEARCH COORDINATOR I - RESEARCH CANCER
Department : Allied Health
Status : Full Time
Shift : 1st
Remote or Onsite : Onsite
Location : Newport Beach, CA, US, 92617
Salary Range : $33.9100-$52.1700 / hour. Actual compensation may vary based on geographic location, work experience, skill level, and education.
Reporting to the Clinical Research Supervisor, Clinical Research Manager, or Director of Clinical Research Operations, the Clinical Research Coordinator I (CRC-I) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. The CRC-I provides support and coordination for FDA regulated research including data, blood and tissue collection studies that may involve industry-sponsored, government funded and / or investigator initiated clinical research trials.
The CRC-I is involved in all aspects of the clinical research process including, but not limited to protocol review, preparation and administration of the informed consent, completion of study related visit forms, ensuring protocol required assessments are completed per study guidelines, processing of lab samples per IATA standards, regular communication with study sponsors and their collaborators, and data entry into study systems within study required timeframes.
The CRC-I will ensure accurate completion of case report forms (CRFs), adverse event / serious adverse event (SAE) reporting, scheduled subject follow-up, and maintenance of regulatory binders. Discusses research study with potential study subjects and answers any questions (may refer questions to Principal Investigator or Sub-Investigator when appropriate) while obtaining informed consent as well as assisting in scheduling follow-up visits for enrolled subjects.
Responsible for development of study flow sheets, preparation of study source documentation, gathering study data, and assessing subject eligibility (inclusion / exclusion). In addition, the CRC-I will record protocol specific assessments and ensure collection and shipment of samples, complete study forms to submit to sponsors and / or appropriate agencies, collect, enter, and clean data into study database while maintaining data quality.
Must be knowledgeable of Good Clinical Practices, protection of human subjects in research practices, and FDA regulatory guidelines regarding clinical research.
Education and Experience
- High School Diploma with sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and / or equivalent experience / training.
- Excellent verbal and written communications and presentation skills; excellent organizational skills; and excellent interpersonal skills to work effectively in a diverse team.
- Proficiency with Microsoft Word, PowerPoint, and Windows.
- Excellent analytical and problem-solving skills.
- Ability to work effectively in a fast-paced, team-based environment; project management and coordination skills; ability to prioritize tasks and meet multiple deadlines on concurrent projects.
- Ability to establish cooperative working relationships with patients, co-workers, and physicians.
Preferred Qualifications :
Hoag is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Hoag is committed to the principle of equal employment opportunity for all employees and providing employees with a work environment free of discrimination and harassment. Hoag hires a diverse group of people in a manner that allows them to reach their full potential in the pursuit of organizational objectives.
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Salary : $34 - $52
