Job Description

Clinical Research Associate 2580199

A leading hospital is seeking a skilled Research Associate - Administration. The successful candidate will oversee, manage and participate in research activities. The ideal candidate has 2+ years of experience in a clinical research coordinator role. . The company offers a great work environment!

Clinical Research Associate Pay and Benefits:

• Hourly pay: $30/hr
• Worksite: Leading hospital and health care system (Los Angeles, CA 90020- Job location may require site to site travel - Santa Monica, Torrance)
• W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
• 40 hours/week, 3 Month Assignment

Clinical Research Associate Responsibilities:

• Provide oversight of clinical research sites compliance with ICH/Good Clinical Practices (GCP), governing SOPs (standard operating procedures) and clinical study protocols.
• Responsible for research assessment and patient intervention under the supervision of the Principal Investigator.
• Responsible for regulatory coordination of clinical research studies, preparation, submission and maintenance of regulatory files to fulfill research requirements.
• Additional responsibilities include regulatory compliance, patient recruitment and enrollment, data collection, research chart documentation, quality assurance, report preparation, protocol information dissemination to health care professionals, patients and their family members.
• Work may be assigned by Senior Management, and assignments may be changed on an as-needed basis in order to ensure that studies and patient care needs are handled appropriately and in a timely manner.
• Travel to other locations may be required.

Clinical Research Associate Qualifications:

• A multi-tasked individual with a minimum 2 years of experience in a clinical research coordinator role.
• College degree in medicine, science, health, or equivalent.
• Performs management of research activities to ensure the collection of accurate clinical data within given timeline.
• Knowledge of ICG GCP guidelines and expertise to review, evaluate medical data and all applicable local laws and regulations.
• Demonstrated knowledge of all components of the research process as it pertains to clinical trials and studies, i.e., IRB procedures and processes, data management, etc.
• Experience in selection and management of vendors/CROs (Central Lab, IVRS, EDC).
• Track progress of clinical studies with regard to budget, study milestones, and deadlines.Recruiting & enrolment of patients who meet eligibility criteria, scheduling, completing CRFs.
• Able to solve complex problems, prioritize multiple tasks, plan proactively and accomplish goals within project in a dynamic team environment.
• Participate in study audits, as applicable.

Clinical Research Associate Shift:

• Monday-Friday, 8:00-5:00

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