Clinical Research Assistant

Temple University • Philadelphia, PA

10h • Onsite

About The Position

Temple University’s Lewis Katz School of Medicine, Pulmonary/Critical Care/Sleep Med Department, is seeking a Clinical Research Assistant to support clinical research projects and trials. The assistant works under the direct supervision of the Principal Investigator and/or Research Coordinators and is mentored by coordinators, managers, and/or the PI. Decisions are made within established policies, procedures, and instructions. The role involves study coordination, patient screening and enrollment support, data collection and entry, documentation, and clerical and technical assistance. Prior clinical research experience is not required, but analytical thinking, attention to detail, and an interest in learning about clinical research are important. This is an on-site, grant-funded position. A background check and PII/Cash Handling Clearance are required before service begins.

Requirements

• Zero to 6 months of related experience, or an equivalent combination of education and experience.
• Strong interest in learning about clinical research.
• Demonstrated computer skills and proficiency with MS Office Suite software programs.
• Aptitude in professionalism.
• Excellent written and oral communication skills.
• Analytical thinking and attention to detail.

Responsibilities

• Assist with screening, enrollment, and tracking patients in clinical trials and other research studies.
• May participate in enrolling human subjects; obtain informed consent; schedule study visits; perform basic clinical assessments; and collect and enter study data.
• Perform research, database, and clerical tasks to support clinical trials and help investigators organize, gather, and compile clinical research data.
• Organize and maintain documentation required for clinical trials and other research projects.
• Inform the Principal Investigator or designated individuals about issues involving patient responses to treatment, medication, or adverse effects.
• Assist the Principal Investigator with Institutional Review Board filings and annual reviews.
• Provide 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.

Benefits

• Full medical coverage
• Dental coverage
• Vision coverage
• Paid time off
• 11 paid holidays
• Tuition remission for eligible employees and their dependents
• Retirement plan

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed