Clinical Research Assistant - Hematology

City of Philadelphia - Philadelphia, PA

Full-time - Entry Level

Philadelphia, PA

1,001-5,000 employees

Executive, Legislative, and Other General Government Support

About the position

The Clinical Research Assistant in Hematology at Jefferson Health plays a crucial role in supporting clinical trials and research initiatives. This position is designed for individuals who are eager to contribute to the advancement of medical knowledge and patient care through research. The assistant will work under the direct supervision of research coordinators, assisting in the organization, gathering, and compilation of clinical research data. This role is essential in ensuring that all research activities adhere to established protocols and regulatory requirements, particularly those set forth by the Institutional Review Board (IRB). In this position, the Clinical Research Assistant will be responsible for tracking and maintaining credentialing documentation for all staff and researchers involved in clinical trials. This includes ensuring compliance with IRB regulations and maintaining the integrity of the research process. The assistant will also provide clerical and technical support to facilitate the smooth operation of clinical trials, ensuring that all data collected is accurate and reliable. The role requires effective communication and interaction with co-workers, visitors, and other staff, embodying the values of Jefferson Health. The assistant will perform a variety of research, database, and clerical duties to support clinical trials, assisting investigators in organizing and compiling clinical research data. Additionally, the assistant will be responsible for maintaining documentation required for clinical trials and will inform the Principal Investigator or designated individual of any issues concerning patient responses to treatment, medication, or any adverse effects observed. The assistant may also assist in the enrollment of human subjects, contributing to the overall success of the research initiatives.

Responsibilities

• Assist research coordinators with organizing, gathering, and compiling clinical research data.
• Track and maintain credentialing documentation for staff and researchers participating in clinical trials in accordance with IRB regulations.
• Provide clerical and technical support to ensure adherence to research protocols and quality of information received.
• Perform a variety of research, database, and clerical duties in support of clinical trials.
• Organize and maintain documentation required for clinical trial(s).
• Inform Principal Investigator and/or designated individual on any issues concerning patient's response to treatment/medication/any adverse effects overall to patients.
• Assist Principal Investigator with IRB filings and annual reviews.
• May assist in the enrollment of human subjects.

Requirements

• Minimum High School Diploma or equivalent.
• Experience in a research or clinical setting preferred.

Nice-to-haves

• Experience in clinical trials.

Benefits

• Vision insurance.