Clinical Research Coordinator/Data Manager

Jefferson Health Plans • Philadelphia, PA

2d • 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.
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 Bachelor’s degree/Master’s degree).

Nice To Haves

• Bachelor’s degree/Master’s degree

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.
• 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)
• 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