Oncology Clinical Research Coordinator – Impactful Trials

Ochsner Health; Baton Rouge (LA); On-site; USD 40,000 - 60,000; Full time

Job summary

Ochsner Health seeks a dedicated research professional to manage clinical trial activities, recruit participants, obtain informed consent, and coordinate visits under supervision. Strong organizational and documentation skills are essential, with familiarity in Epic and regulatory standards.

The role requires a high school diploma (or equivalent) and 1 year of relevant experience or a life sciences degree, plus BLS certification within 60 days. Remote exceptions may apply.

Qualifications

• Knowledge of medical and clinical research terminology and processes.
• Familiarity with ICH guidelines for ethical conduct of research.
• Ability to follow the investigational plan in execution of study visits.
• Strong organizational and time management skills and ability to multi-task and pay close attention to detail.

Responsibilities

• Assists in recruiting study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings as required.
• Coordinates and oversees patient activity as it relates to the conduct of research and clinical trials including informed consent under direction and supervision of more senior research staff.
• Arranges necessary tests and procedures in accordance with protocol requirements and reports results to the investigator.
• Performs clinical laboratory activities as required per protocol.
• Develops and maintains all required documentation as it relates to the conduct of assigned clinical trials and associated patient care.
• Completes data entry into sponsor-specific data entry systems and/or supports data coordinator, including query resolution.
• Conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines.
• Adapts behavior to the specific patient population and respects privacy, etc.
• Performs other related duties as assigned.

Skills

Medical terminology

ICH guidelines

Documentation

Data entry

Verbal communication

Attention to detail

Travel between facilities

Computer proficiency

Education

High school diploma or equivalent

Bachelor's degree in life science or related field

Tools

Epic

Job description

Ochsner Health seeks a dedicated research professional to manage clinical trial activities, recruit participants, obtain informed consent, and coordinate visits under supervision. Strong organizational and documentation skills are essential, with familiarity in Epic and regulatory standards.

The role requires a high school diploma (or equivalent) and 1 year of relevant experience or a life sciences degree, plus BLS certification within 60 days. Remote exceptions may apply.