Associate Clinical Research Coordinator - Oncology

About the role

This job evaluates, initiates, and maintains activities related to the conduct of clinical trials with the assistance and guidance of departmental staff. It involves communicating with external funding agencies and sponsors, other departments, departmental staff, and patients to ensure understanding of the requirements of conducting and participating in clinical trials.

Responsibilities

• Affords study participants and screens them for eligibility on the telephone, in the clinic, and other settings as required.
• Coordinates and oversees patient (study participant) 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, including but not limited to respect for privacy, method of introduction to the patient, adapting explanation of services or procedures to be performed, requesting permissions and communication style.
• Performs other related duties as assigned.

Requirements

• Education Required – High school diploma or equivalent.
• Work Experience Required – 1 year of relevant research or clinical experience, OR Bachelor's degree in life science or related field.

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.
• Knowledge of the requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.
• Effective verbal and written communication skills.
• Organizational and time management skills and ability pay close to detail.
• Ability to travel throughout and between facilities and work a flexible work schedule.

Skills

• 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.
• Knowledge of the requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Proficiency in using computers, software, and web-based applications, including working knowledge of Epic.
• Effective verbal and written communication skills.
• Organizational and time management skills and ability pay close to detail.
• Ability to travel throughout and between facilities and work a flexible work schedule.

Benefits

At Ochsner, we offer competitive benefits packages designed to help you maintain your health and well-being. These benefits include:

• Health insurance coverage
• Dental and vision insurance
• Paid time off
• Flexible spending accounts
• Retirement savings plans
• Employee assistance programs

Pay

The salary range for this position is $XX/X based on experience and qualifications. Final compensation will be determined based on the successful candidate’s qualifications and experience.

Schedule

The schedule for this position is typically Monday through Friday, with occasional evenings and weekends as needed. Flexible scheduling may be available for certain positions.