Clinical Research Professional (I, II or III) Department of Internal Medicine, Division of Pulmonary
- Plan and coordinate clinical research projects.
- Screen patients for admittance in study based on pre-determined criteria.
- In conjunction with the investigator, document and evaluate adverse events and response to treatment.
- Coordinate the generation of data for proposals, reports, and manuscripts. Assist in development of reports.
- Perform routine physical/clinical procedures.
- Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati (UC)/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
- Maintain regulatory documentation. Prepare IRB submissions.
- Draft subject informed consents and consent comprehension tests. Assist in drafting compliant advertisements.
- Liaison with medical staff, university departments, ancillary departments, satellite facilities, IRB, and industry contacts.
- Provide direction, instruction and guidance to coordinate research activities, including patient screening and recruitment, enrollment and education. Ensure protocol procedures have been completed adhering to Good Clinical Practice Guidelines as defined by the Federal Drug Administration (FDA) and serve as subject matter expert.
- Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations. Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.
- Assist with developing and revising policies and procedures for the research team to ensure compliance with the protocol.
- Serve as a resource within the department for the development of less experienced team members.
- Contribute to the development of new processes, procedures, tools and training to enhance clinical research activities, compliance, and efficiency.
- Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
- Perform related duties based on departmental need. This job description can be changed at anytime.
- Provide direction, instruction and guidance to coordinate research activities including patient screening and recruitment, enrollment and education. Ensure protocol procedures have been completed adhering to Good Clinical Practice Guidelines as defined by the Federal Drug Administration (FDA) and serve as subject matter expert.
- Independently coordinate nursing/social work and patient care and/or patient follow-up functions of the clinical study including planning and developing related activities. Provide quality patient care to patients and their families within area of clinical specialty.
- Collaborate with care coordinators, social workers, psychologists, physicians and other appropriate treatment team members in diagnostic formulation, treatment direction, and recommendations. Act as a liaison with medical staff, university departments, ancillary departments and/or satellite facilities.
- Initiate and assist with developing and revising policies and procedures for nursing practice.
- Serve as a peer-mentor within the department, supporting management and in various responsibilities as appropriate including the development of less experienced team members.
- Contribute to the development of new processes, procedures, tools and training to enhance clinical research activities, compliance, and efficiency.
- Ensure compliance with contract principles, federal regulations, laws and University of Cincinnati/University of Cincinnati Physicians Company (UCPC) policy and operating procedures.
- Perform related duties based on departmental need. This job description can be changed at any time.
- Bachelor's Degree must be in a related field.
- Five (5) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
- Bachelor's Degree must be in a related field.
- Seven (7) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
- Bachelor's Degree must be in a related field.
- Nine (9) years of relevant education, experience and/or other specialized training can fulfill minimum education and experience requirements
- One (1) year of related experience.
- Three (3) years relevant experience
- Five (5) years of relevant experience
- SoCRA/ACRP/RAPS certification
- For patient facing role, CPR certification
- Experience in an academic or clinical setting in the area of clinical specialization.
- Master's Degree
- Experience in an academic or clinical setting in the area of clinical specialization.
- Office environment/no specific unusual physical or environmental demands.
- Competitive salary based on experience
- Comprehensive health coverage (medical, dental, vision, prescription)
- Flexible spending accounts & wellness programs
- Professional development & mentorship opportunities
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