Clinical Research Coordinator jobs in Lorain, OH

Job Summary:

Responsibilities:

• Coordinate the implementation and conduct of research projects ensuring adherence to research protocol requirements including timely completion and communication of regulatory documents, the development of data capture and monitoring plans, reports Serious Adverse Events as they occur and completion of Food and Drug Administration (FDA) and sponsor forms in accordance with GCP guidelines. 
• Serves as a liaison between investigators, research personnel, outside study personnel and central research administration offices to assist in protocol interpretation, enrollment and safety questions. 
• Utilizes the nursing process as a basis for patient care.
• Assesses research subject; completes nursing assessment, documenting findings in research subject records. Notifies physician of abnormal findings.
• Establishes a care plan in collaboration with the research subject, family and research team.  Coordinates ongoing care.
• Identifies discharge needs and facilitates discharge planning as appropriate.
• Performs telephone triage. 
• Performs nursing procedures and treatments as directed by physician or LIP in the treatment and management of patient care. 
• Evaluates, initiates and maintains standards of care consistent with CCHS policies & procedures.
• Assists with specialized patient care equipment as required by the clinical research protocol.
• Administers medications and treatments as ordered by a physician or LIP. 
• Directs, coordinates and participates in the evaluation & supervision of nursing care provided to research subjects, establishing patient care priorities and delegating nursing activities according to the patient needs and staff qualifications and capabilities. 
• Participates in education, research and performance improvement activities.
• Develops and maintains knowledge of research protocol to coordinate the comprehensive and compliant execution of assigned protocols. 
• Assists with preparation for audits and response to audits.
• Maintains professional relationships, including frequent and open effective communication with internal and external customers.
• Assists with the development of training and educational material for assigned research protocols.  Provides and documents education as needed.
• Develops protocol specific checklists. 
• Educates the patient/family and team on the research protocol. 
• Conducts and documents the informed consent process.
• May assist PI with research study design and development of the research protocol.
• May assist with research project budget development.
• Performs other duties as assigned.

Education:

• Graduate from an accredited school of professional nursing. 
• BSN preferred.

Certifications:

• Current state licensure as Registered Nurse (RN). 
• Proof of Basic Life Support (BLS) certification must be presented upon hire. 
• Any registered nurse or advanced practice nurse must obtain a cancer specific certification or demonstrate ongoing qualifying education within the timeframe of the facilities accreditation cycle, if they work in  medical oncology, radiation oncology,  cancer center or cancer clinic and/or administer chemotherapy within an accredited Cleveland Clinic facility.

Complexity of Work:

• Demonstrates basic computer proficiency.
• Must have strong organizational, communication and interpersonal skills.
• Must be self-directed with demonstrated ability to work effectively with a multidisciplinary team of professionals.
• Ability to work with minimal supervision at offsite facilities.
• Displays a thorough understanding of the research process and terminology, and in-depth knowledge of the specialty under investigation.
• Exhibits a working knowledge of federal regulations and good clinical practice (GCP).
• Meets clinical competency requirements. 
• Maintains current knowledge in specialty area.
• Participates in process improvement activities.
• Continually demonstrates competency with defined requirements for the position as established by Cleveland Clinic.

Work Experience:

• Four years clinical experience and two years research experience.

Physical Requirements:

• Requires full range of body motion, manual and finger dexterity, and eye-hand coordination.
• Requires standing and walking for extended periods of time.
• Requires corrected vision and hearing to normal range.
• Requires working under stressful conditions and irregular hours.
• Exposure to communicable diseases and/or body fluids.
• Medium Work - Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Physical Demand requirements are in excess of those for Light Work.

Personal Protective Equipment:

• Follows standard precautions using personal protective equipment as required