Clinical Research Coordinator

Jefferson Health Plans • Philadelphia, PA

4d • Onsite

About The Position

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.

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 the quality of information received.

Requirements

• 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.
• High school diploma with at least 5 years of research experience OR Bachelor's of science/master’s degree preferred; Some clinical experience preferred

Nice To Haves

• Some clinical experience preferred

Responsibilities

• 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.
• Performs routine operational tasks as needed and acts as back-up coordinators on other clinical trials.
• 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.

Benefits

• Medical (including prescription)
• Supplemental insurance
• Dental
• Vision
• Life and AD&D insurance
• Short- and long-term disability
• Flexible spending accounts
• Retirement plans
• Tuition assistance
• Voluntary benefits (group rates on insurance and discounts)
• Tuition discounts at Thomas Jefferson University after one year of full time service or two years of part time service

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED