CLinical Research Coordinator- PKPD

Thomas Jefferson University & Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 40,000 - 70,000; Full time

Job summary

An established industry player is seeking a Clinical Research Coordinator to oversee clinical trial activities. This role involves managing databases, processing biological specimens, and assisting investigators in gathering and compiling clinical research data. The ideal candidate will have a strong background in clinical trial support, ensuring quality data and adherence to protocols. Join a leading healthcare organization committed to advancing research and education while making a difference in patient care. If you are passionate about clinical research and eager to contribute to innovative healthcare solutions, this opportunity is perfect for you.

Qualifications

• Experience in clinical trial support and data management.
• Ability to assist in regulatory filings and patient enrollment.

Responsibilities

• Oversees day-to-day activities of clinical trials.
• Maintains documentation and informs investigators of patient issues.
• Provides clerical support to ensure adherence to research protocols.

Skills

Database Management

Biospecimen Processing

Clerical Duties

Regulatory Filings

Patient Interaction

Education

High School Diploma or equivalent

Bachelor's Degree

Master's Degree

Job description

Job Details

CLinical Research Coordinator- PKPD

Job Description

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.

1. Performs research, database management, 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.
2. Organizes and maintains documentation required for clinical trial(s).
3. Informs the Principal Investigator and/or designated individual of any issues concerning patients' response to treatment/medication or adverse effects.
4. Assists the Principal Investigator with regulatory filings, including IRB submissions.
5. May assist in the enrollment of human subjects.
6. Provides clerical and technical support to ensure adherence to research protocols and quality of data.

Education:

Minimum High School Diploma or equivalent.

Experience:

High School Diploma or equivalent with 4 years of relevant experience, or a Bachelor's/Master's degree with preferred prior experience.

Work Shift:

Day shift (United States of America)

Worker Sub Type:

Regular

Primary Location Address:

1015 Chestnut Street, Philadelphia, Pennsylvania, United States of America

Jefferson, located in the Philadelphia region, Lehigh Valley, Northeastern Pennsylvania, and southern New Jersey, is reimagining healthcare and higher education to create value. With over 65,000 staff, Jefferson provides high-quality clinical care, advances research, and educates future professionals across its colleges and schools, serving more than 8,300 students.

Jefferson Health is a top-ranked not-for-profit healthcare system serving the region through numerous hospitals and outpatient locations. Jefferson Health Plans offers health coverage options in Pennsylvania and New Jersey.

Jefferson is committed to equal opportunity employment and education, welcoming all qualified applicants regardless of age, race, color, religion, sexual orientation, gender identity, marital status, pregnancy, national origin, military or veteran status, disability, or other protected status.