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

Jefferson Health; Philadelphia (Philadelphia County); On-site; USD 70,000 - 110,000; Full time

Job summary

An established industry player in healthcare is seeking a Clinical Research Project Manager to lead clinical trials from inception to completion. This vital role involves overseeing daily trial activities, ensuring compliance with Good Clinical Practice, and training research staff. You will manage data integrity and regulatory submissions while representing the organization both internally and externally. Join a dedicated team committed to advancing healthcare and making a significant impact in the field of clinical research. If you're passionate about improving patient outcomes and thrive in a collaborative environment, this opportunity is perfect for you.

Qualifications

• 5+ years of clinical research experience with a Bachelor's degree.
• Master's degree with 3 years of clinical research experience.

Responsibilities

• Oversee clinical trials ensuring compliance with GCP.
• Train staff on GCP procedures and maintain subject logs.
• Prepare IRB and regulatory submissions for compliance.

Skills

Clinical Research Management

Data Management

Regulatory Compliance

Staff Training

Quality Control

Education

Bachelor's Degree

Master's Degree

Tools

Electronic Data Capture Systems

Job description

Below is a refined version of the job description, with improved formatting and focus on relevant content:

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

Location: Jefferson, Philadelphia, PA

Type: Full-time

Posted: 2 Days Ago

Job Details

The Clinical Research Project Manager will independently 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. Ensuring all study procedures comply with protocols and regulations is essential. The role involves training and supervising research staff, overseeing clinical trials, developing standard operating procedures, and representing TJU internally and externally.

Responsibilities

• Oversee day-to-day activities of clinical trials in accordance with Good Clinical Practice (GCP).
• Train and supervise research staff on GCP procedures.
• Prepare and submit IRB and regulatory materials to ensure compliance.
• Maintain accurate subject logs, track expenses, and coordinate with Grant Administrators.
• Perform quality control assessments to ensure data integrity.
• Organize and maintain patient data documentation.
• Design and manage electronic data capture databases.
• Provide clerical and technical support to adhere to research protocols.

Qualifications

Bachelor’s degree with 5 years of clinical research experience or Master’s degree with 3 years of experience.

Work Details

Shift: Day shift (United States)

Location: 1101 Market, Philadelphia, PA

About Jefferson

Jefferson is a nationally ranked health system committed to reimagining healthcare and higher education. With over 65,000 staff, Jefferson provides high-quality clinical care, education, and research across multiple campuses and locations. The organization is dedicated to equal opportunity employment and fostering a diverse workforce.