Clinical Research Assistant-Recruitment

This position is on-site and requires a background check.

About the Role

The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. The Clinical Research Assistant is mentored by coordinators, managers and/or the PI. Decisions are made within the limits of clearly established policies, procedures or instructions. This is a grant-funded position.

At Temple University's Lewis Katz School of Medicine, you will be part of a nationally recognized, state-of-the-art research community that is driving innovation in patient care. Our clinical research programs span a wide range of disciplines and provide coordinators with the opportunity to contribute to groundbreaking studies that directly impact the health and well-being of diverse populations. With access to advanced resources, collaborative teams, and a strong commitment to excellence, Temple offers an ideal environment for Clinical Research Coordinators to grow their careers while shaping the future of medicine.

Responsibilities

• Perform study coordination tasks under direct supervision, following established protocols and procedures.
• Assist with screening, enrollment, and tracking patients in clinical trials and other research studies.
• Participate in the enrollment of human subjects for clinical trials, including obtaining informed consent, scheduling subjects for visits, performing basic clinical assessments, and collecting and entering study data.
• Perform various research, database, and clerical tasks to support clinical trials, aiding investigators in organizing, gathering, and compiling clinical research data.
• Organize and maintain documentation required for clinical trials and/or other research projects.
• Inform the Principal Investigator or other designated individuals about any issues regarding patient responses to treatment, medication, or adverse effects.
• Assist the Principal Investigator with Institutional Review Board (IRB) filings and annual reviews.
• Offer clerical and technical support to ensure adherence to research protocols and maintain the quality of information received.
• Adhere to FDA, IRB, Pennsylvania, and other applicable regulations.
• Perform other duties as assigned.

Requirements

• Zero to 6 months of related experience is required, or an equivalent combination of education and experience may be considered.
• Strong interest in learning about Clinical Research.
• Demonstrated computer skills and proficiency with MS Office Suite software programs.
• Excellent written and oral communication skills.
• Aptitude in professionalism.

Benefits

• Full medical, dental, and vision coverage.
• Paid time off.
• 11 paid holidays.
• Tuition remission – eligible employees and their dependents can obtain a degree tuition-free.
• Generous retirement plan.

Pay

Salary Range: Up to $49,000.00 per year. A variety of important factors are reviewed by HR when considering salary, including job duties, the applicant's education and experience, all relevant internal equity considerations, department budget, and funding source.