Clinical Research Specialist
2 weeks ago
Clinical Research Associate
A prominent healthcare organization is in search of a proficient Clinical Research Associate to lead, manage, and engage in research initiatives within the Department of Medicine Clinical Trial Program. The ideal candidate will possess a minimum of two years of experience in clinical research coordination within an academic medical environment.
Compensation and Benefits:
- Hourly wage: $30/hr
- Work environment: Esteemed healthcare institution
- Employment type: W2, with Group Medical, Dental, Vision, Life, Retirement Savings Program, Paid Sick Leave
- Full-time: 40 hours/week, with a 3-month contract (potential for extension)
Key Responsibilities:
- Ensure compliance of clinical research sites with ICH/Good Clinical Practices (GCP), relevant SOPs, and clinical study protocols.
- Conduct research evaluations and patient interventions under the guidance of the Principal Investigator.
- Oversee the regulatory management of clinical research projects, including the preparation, submission, and upkeep of regulatory documentation.
- Coordinate research activities to guarantee the collection of precise clinical data within specified timelines.
- Additional duties encompass regulatory adherence, patient recruitment and enrollment, data gathering, research documentation, quality assurance, report generation, study audits, and dissemination of protocol information to healthcare professionals and patients.
Qualifications:
- Minimum of 2 years of experience in a clinical research coordinator capacity within an academic medical setting.
- Bachelor's degree in medicine, science, health, or a related field.
- Familiarity with IRB procedures, patient recruitment, enrollment, and completion of CRFs.
- Understanding of ICG GCP guidelines and ability to assess and interpret medical data alongside applicable local regulations.
- Comprehensive knowledge of the research process as it relates to clinical trials, including IRB procedures and data management.
- Experience in vendor/CRO selection and management.
- Proficient in tracking clinical study progress concerning budget, milestones, and deadlines.
- Skilled in recruiting and enrolling eligible patients, as well as scheduling and completing CRFs.
- Adept at resolving complex issues, prioritizing multiple tasks, planning proactively, and achieving project goals within a collaborative team setting.
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