Clinical Research Project Manager (Lung Center, Sidney Kimmel Cancer Center)

Thomas Jefferson University & Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 60,000 - 100,000; Full time

Job summary

An established industry player is seeking a dedicated Clinical Research Coordinator to oversee clinical trials from inception to completion. This role encompasses protocol coordination, data management, and regulatory compliance, ensuring that all study procedures adhere to Good Clinical Practice (GCP). You will play a pivotal role in training research staff and maintaining high standards of data quality. Join a dynamic team in a leading healthcare organization that values innovation and excellence in clinical research, making a significant impact on patient care and education in the healthcare sector.

Qualifications

• 5+ years of clinical research experience or 3+ years with a Master's degree.
• Strong understanding of Good Clinical Practice (GCP) guidelines.

Responsibilities

• Conduct clinical trials from startup to closeout, ensuring compliance.
• Train and supervise research staff on GCP procedures.
• Maintain accurate subject logs and track expenses.

Skills

Clinical Trial Management

Data Management

Regulatory Compliance

Staff Training

Quality Control

Education

Bachelor's Degree

Master's Degree

Tools

Electronic Capture Databases

Job description

Job Details

Job Description

Works independently to conduct clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and IRB document preparation. Ensures all study procedures are conducted according to the protocol and applicable regulations. Trains and supervises research staff, oversees clinical trials from start-up to closeout, and develops or contributes to standard operating procedures and processes. Attends leadership meetings, represents TJU internally and externally, oversees research operations in a division or department, and provides expert consulting at an institutional level.

• Oversees the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).
• Trains research staff on proper procedures for conducting a clinical trial per GCP.
• Prepares and submits all materials for the Institutional Review Board (IRB) and other regulatory bodies to ensure compliance.
• Maintains accurate subject logs, tracks expenses, and submits documentation to the Grant Administrator monthly for study visit payments.
• Performs regular quality control assessments to ensure clinical trial data is collected and stored per GCP.
• Organizes and maintains documentation of all patient data.
• Designs electronic capture databases and manages all collected data.
• Provides clerical and technical support to ensure adherence to research protocols and data quality.

Qualifications: Bachelor's degree with 5 years of clinical research experience, or Master's Degree with 3 years of clinical research experience.

Work Shift

Day shift (United States of America)

Worker Sub Type

Regular

Primary Location Address

1101 Market, Philadelphia, Pennsylvania, United States of America

Jefferson, located in the greater 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 10 colleges and 3 schools, serving more than 8,300 students.

Jefferson Health, ranked among the top 15 non-profit healthcare systems nationally, operates 32 hospital campuses and over 700 outpatient locations, serving millions annually. Jefferson Health Plans offers a broad range of health coverage options in Pennsylvania and New Jersey for over 35 years.

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