Clinical Trials Coordinator: Data, Recruits & Visits

Thomas Jefferson University & Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Life and AD&D insurance

Disability insurance

Tuition assistance

Retirement plans

Job summary

Thomas Jefferson University is seeking a detail-oriented professional to oversee day-to-day clinical trial activities under GCP. The role includes data management, biospecimen processing, and clerical duties to support investigators in organizing and compiling trial data.

Recruits and consents subjects and conducts study visits as part of the study team. The position requires light supervision, strong adherence to research protocols, and the ability to coordinate regulatory filings and subject

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, data base, 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.

Education

High School Diploma/GED or equivalent

Job description

Thomas Jefferson University is seeking a detail-oriented professional to oversee day-to-day clinical trial activities under GCP. The role includes data management, biospecimen processing, and clerical duties to support investigators in organizing and compiling trial data.

Recruits and consents subjects and conducts study visits as part of the study team. The position requires light supervision, strong adherence to research protocols, and the ability to coordinate regulatory filings and subject