Clinical Research Nurse 1 Baptist Jacksonville

Baptist Health Jacksonville; Jacksonville (FL); On-site; USD 65,000 - 90,000; Full time

Job summary

Baptist Health Jacksonville is seeking an Oncology Research Nurse to oversee clinical oncology studies at our Downtown Jacksonville campus. You will coordinate study activities, ensure regulatory compliance and safeguard participant safety in line with GCP and sponsor specifications.

This role requires strong organizational skills, the ability to manage multiple protocols, and collaboration with investigators, coordinators and regulators to maintain study integrity.

Qualifications

• Minimum 1 year clinical and/or research experience required.
• Bachelor's Degree may substitute one year of research experience.
• Familiar with Good Clinical Practice guidelines, FDA regulations and subject protection standards.

Responsibilities

• Coordinate study-related activities across clinical, regulatory and administrative tasks.

Skills

Oncology research coordination

GCP compliance

Regulatory knowledge

Education

Bachelor's degree

Job description

Job Description:

Experience, qualification, and soft skills, have you got everything required to succeed in this opportunity Find out below.

About Baptist Health

Recognized as a top place to work in health care, Baptist Health cares for more patients in Northeast Florida than any other provider, ranking as "most preferred" for more than 30 years. We're Jacksonville's only locally governed, faith-based, not-for-profit health system and provide a full spectrum of preventive and specialty care through 200+ locations and six hospitals. Our centers of excellence include Baptist MD Anderson Cancer Center, Baptist Heart Hospital, Baptist Neurological Institute and Wolfson Children's Hospital.

Responsible for the conduct of oncology research activities throughout BMDACC. The Oncology Clinical Research Nurse ensures that research is conducted in accordance with established standards by working with clinical investigators to coordinate study-related activities. These activities will be clinical, regulatory and administrative in nature. Coordinates numerous protocols simultaneously. She/he will ensure assigned protocols are consistent with Good Clinical Practice Guidelines (BCP), Federal Food and Drug Administration (FDA), local regulations, institutional policies and procedures, and sponsor specifications. Maintain knowledge of clinical practice standards, oncology nursing practice standards, JCAHO related safety requirements, OHRP requirements, human subject protection standards, and all institutional policies and procedures.

xzgxqkn Note: Minimum 1 year clinical and/or research experience required. Bachelor's Degree may substitute one year research

Primary Location

Downtown - Pavilion836 Prudential DrJacksonville, FL 32207United States of America