Research Associate

1 week ago


Los Angeles, California, United States Avispa Technology Full time
Research Associate - Clinical Trials
A reputable healthcare organization is in search of a proficient Research Associate specializing in clinical trials. The successful applicant will be responsible for overseeing, managing, and actively participating in various research initiatives. The ideal candidate will possess the necessary skills and experience to excel in this role. The organization provides a supportive work environment.

Compensation and Benefits for Research Associate:

Hourly Compensation:
$30/hr

Work Environment:
Esteemed healthcare organization (location may involve travel between sites)
W2 Employment, Group Medical, Dental, Vision, Life Insurance, Retirement Savings Program, Paid Sick Leave
40 hours/week, Temporary Assignment

Key Responsibilities of the Research Associate:


Ensure compliance of clinical research sites with ICH/Good Clinical Practices (GCP), relevant SOPs (standard operating procedures), and clinical study protocols.

Conduct research assessments and patient interventions under the guidance of the Principal Investigator.
Manage regulatory coordination for clinical research studies, including preparation, submission, and maintenance of regulatory documentation to meet research standards.

Additional duties encompass regulatory compliance, patient recruitment and enrollment, data collection, research documentation, quality assurance, report generation, and dissemination of protocol information to healthcare professionals, patients, and their families.

Tasks may be assigned by Senior Management, with the possibility of adjustments as necessary to ensure timely handling of studies and patient care needs.

Travel to various locations may be necessary.

Qualifications for the Research Associate:
A versatile individual with a minimum of 2 years of experience in a clinical research coordinator capacity.
A degree in medicine, science, health, or a related field.
Ability to manage research activities to guarantee the collection of precise clinical data within established timelines.
Familiarity with ICG GCP guidelines and the ability to review and evaluate medical data in accordance with applicable local laws and regulations.

Proven understanding of all aspects of the research process related to clinical trials and studies, including IRB procedures, data management, etc.

Experience in selecting and managing vendors/CROs (Central Lab, IVRS, EDC).
Monitor the progress of clinical studies concerning budget, study milestones, and deadlines.
Recruit and enroll patients who meet eligibility criteria, schedule appointments, and complete case report forms.

Capable of resolving complex issues, prioritizing multiple tasks, planning proactively, and achieving goals within a dynamic team environment.

Participate in study audits as required.

Work Schedule:
Monday-Friday, 8:00 AM - 5:00 PM

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