Clinical Research Coordinator - (Variable Time, Family and Community Medicine

Jefferson Health Plans • Philadelphia, PA

1d • Onsite

About The Position

Works under limited supervision and oversees the day-to-day activities of a clinical trial in accordance with Good Clinical 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. 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.

Requirements

• Minimum High School Diploma or equivalent.
• 4 years of relevant experience (with High School Diploma or equivalent).
• Previous experience preferred (with Bachelors degree/Masters degree).

Nice To Haves

• Bachelors degree/Masters degree and previous experience preferred.

Responsibilities

• Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical 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.
• Interacts with co-workers, visitors, and other staff consistent with the values of Jefferson.
• 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.

Benefits

• Medical (including prescription) insurance
• Supplemental insurance
• Dental insurance
• Vision insurance
• 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: Part-time
• Career Level: Mid Level
• Education Level: High school or GED