Clinical Trials Coordinator II - Patient-Focused Studies

Thomas Jefferson University; United States; On-site; USD 42,000 - 62,000; Full time

Benefits offered by this job

Medical insurance

Tuition assistance

Retirement plans

Job summary

Thomas Jefferson University seeks a Clinical Research professional to oversee day-to-day activities of clinical trials in line with GCP. You will support investigators with data collection, database management, biospecimen handling, and regulatory filings, including IRB submissions.

The role involves recruiting and consenting subjects, coordinating study visits, and ensuring compliance with healthcare regulations while maintaining meticulous trial documentation and data integrity.

Qualifications

• High School Diploma/GED or equivalent.
• 4 years of relevant experience.
• Knowledge of and the ability to utilize technology tools to organize, store and manage database systems.
• Knowledge of and ability to utilize tools, techniques and processes for gathering and reporting data in a particular department or division of a company.
• Knowledge and understanding of legislation and regulatory bodies affecting healthcare practices.
• Knowledge of principles and practices associated with the rights and responsibilities of patients and caregivers.
• Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.

Responsibilities

• Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson.
• Performs a variety of research, database, biospecimen collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.
• Organizes and maintains documentation required for clinical trial(s).
• Informs Principal Investigator and/or designated individual on any issues concerning patients response to treatment/medication/ any adverse effects overall to patients.
• Assists Principal Investigator with regulatory body filings including IRB submissions.
• May assist in the enrollment of human subjects.
• May provide clerical and technical support to ensure adherence to research protocols and quality of information received.

Skills

Database management

Data collection & reporting

Regulatory knowledge

Attention to detail

Multitasking

Education

High School Diploma or GED

Tools

Database software

Job description

Thomas Jefferson University seeks a Clinical Research professional to oversee day-to-day activities of clinical trials in line with GCP. You will support investigators with data collection, database management, biospecimen handling, and regulatory filings, including IRB submissions.

The role involves recruiting and consenting subjects, coordinating study visits, and ensuring compliance with healthcare regulations while maintaining meticulous trial documentation and data integrity.