Clinical Research Coordinator

Clinical Trial Coordinator

Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP). Performs a variety of research activities in support of clinical trials (including database management, biological specimen processing, and clerical duties) to assist investigators in organizing, gathering and compiling clinical research data. Recruits, assists with consenting subjects, and conducts study visits. Willing to perform routine operational tasks as needed and act as back-up coordinators on other clinical trials. Must have a good attention to detail as well as good interpersonal skills

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 the quality of information received.

Competencies (Knowledge, Skills, and Abilities Required):

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.

Knowledge and understanding of legislation and regulatory bodies affecting research studies.

Ability to manage multiple concurrent objectives, projects, groups, or activities, making effective judgments as to prioritizing and time allocation.

Scientific writing and reading skills.

Minimum Education and Experience Requirements:

High school diploma with at least 5 years of research experience OR

Bachelor's of science/master's degree preferred; Some clinical experience preferred

Work Shift

Workday Day (United States of America)

Worker Sub Type

Regular

Employee Entity

Thomas Jefferson University

Primary Location Address

900 Walnut Street, Philadelphia, Pennsylvania, United States of America

Jefferson is committed to providing equal educational and employment opportunities for all persons without regard to age, race, color, religion, creed, sexual orientation, gender, gender identity, marital status, pregnancy, national origin, ancestry, citizenship, military status, veteran status, handicap or disability or any other protected group or status.