Clinical Research Coordinator

Tenet Healthcare Corporation • Delray Beach, FL

13d

About The Position

The Clinical Research Coordinator (CRC) assists the Principal Investigator in conducting all aspects of clinical trials, including regulatory tasks, under the direct supervision of the Clinical Research Manager and affiliated Director. The CRC provides operational support in managing patients accrued to multiple research protocols to help ensure subject safety and regulatory compliance. Responsibilities include compiling, registering, and submitting data; monitoring compliance with protocols, Standard Operating Procedures, and applicable regulations and guidelines; and ensuring effective data flow associated with research protocols.

Requirements

• Associate of Science degree or higher in science, healthcare, or a related field; graduates of foreign medical schools are also eligible.
• Strong problem-solving, analytical, and process-management skills.
• Strong planning, organizational, and project-management skills.
• Strong interpersonal and oral and written communication skills.
• Attention to detail and ability to manage multiple priorities.
• Ability to work without close supervision or guidance and exercise independent judgment.
• General PC skills.
• AHA Basic Life Support (BLS) certification within 90 days of hire.
• SOCRA Certified Clinical Research Associate (CCRP) certification within 30 months of hire.

Nice To Haves

• Two to three years of clinical research experience, including healthcare compliance, research auditing, monitoring standards, or related experience.
• Knowledge of federal and state laws governing research.
• Knowledge and understanding of CPT and ICD-10 codes.
• Experience reviewing medical record documentation for accuracy and compliance with laws, rules, policies, and procedures.

Responsibilities

• Report for scheduled shifts on time and prepared to assume responsibilities.
• Attend and participate in meetings and take responsibility for information communicated at meetings.
• Adhere to corporate, regional, hospital, and departmental policies and procedures.
• Assist patients, family members, physicians, visitors, and employees in a professional and courteous manner.
• Follow infection-control procedures.
• Adhere to environmental care standards.
• Adapt to varied age-specific patient populations.
• Fulfill HICS responsibilities, assignments, tasks, and roles as directed during emergencies or disasters; know hospital emergency codes and take appropriate actions in accordance with hospital policies and procedures; participate on an assigned Hurricane response team.
• Comply with HIPAA policies and procedures, including minimum-necessary requirements for the position.
• Support clinical trials, including regulatory tasks, under the supervision of the Clinical Research Manager and affiliated Director.
• Provide operational support for patients enrolled in multiple research protocols, supporting subject safety and regulatory compliance.
• Compile, register, and submit data; monitor protocol and regulatory compliance; and ensure effective data flow for research protocols.

Benefits

• Medical, dental, vision, and life insurance.
• 401(k) retirement savings plan with employer match.
• Paid time off.
• Career development and continuing education opportunities.
• Health savings accounts and healthcare and dependent flexible spending accounts.
• Employee Assistance Program and employee discount program.
• Voluntary benefits, including pet insurance, legal insurance, accident and critical illness insurance, long-term care, elder and childcare, and auto and home insurance.

What This Job Offers

• Education Level: Associate degree