Clinical Research Coordinator
US-ID-Boise
careers
Req #: 99503
Type: Full-Time
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Overview: Our patients come from all walks of life and so do we! We foster an environment that embraces our employees' unique strengths, experiences and perspectives which drive our exceptional patient-centered care. We strive to build a positive, supportive, and inclusive culture to deliver exceptional patient experiences and create a strong work environment. What to Expect: Children and Adult Specialty Research encompasses a variety of indications, including adult and pediatric trials for endocrine diseases, cystic fibrosis (CF), and pulmonary diseases in both outpatient and inpatient settings. The primary focus of this position is the coordination of pulmonology inpatient treatment trials. The candidate must be available for occasional weekend hours, depending on the study and enrollment quantity, and should be flexible to work between inpatient (both floor and ICU) and outpatient clinical trials. A successful candidate will be someone who craves variety in their work and wants to integrate and collaborate with team members across multiple studies within the department. * Conducts and documents informed consent process. * Reviews clinical records and extracts necessary data to determine eligibility and complete data submission via the appropriate mechanism. * Assists in recruiting patients for clinical trials. * Conducts research activities per protocol. * Documents research process, adverse event grading, consent process, patient progress on study in electronic medical record. * Initiates and submits Serious Adverse Events reports to study sponsor in collaboration with the physician and/or principal investigator. * Maintains clinical trials management system; prepare reports as needed. * Prepares for and conducts study monitor visits and audits. * Serves as liaison and reference to physicians, investigators and other staff members for questions regarding the research process. * Collaborates with investigator and regulatory staff regarding Institutional Review Board requirements. * Participates in protocol design, development, and writing, as well as writing study manuscripts. May complete scientific literature searches and due diligence practices prior to study inception. * Prepares basic statistical reports or other reports and presentations as required. * Collaborates with external community, business and academic partners. * Works constructively with coworkers and clinicians to improve processes and standards of practice. * Perform other duties and responsibilities as assigned. Minimum Qualifications: * Education: Bachelor's degree. * Experience: 3 years' experience. * Licenses/Certifications: Current Basic Life Support (BLS) Provider Certified through American Safety and Health Institute, American Heart Association, or American Red Cross. Responsibilities: The Clinical Research Coordinator 2 is responsible for identifying eligible patients for research and ensuring that research protocols are carried out accurately. * Conducts and documents informed consent process. * Reviews clinical records and extracts necessary data to determine eligibility and complete data submission via the appropriate mechanism. * Conducts research activities per protocol. * Documents research process, adverse event grading, consent process, patient progress on study in electronic medical record. * Initiates and submits Serious Adverse Events reports to study sponsor in collaboration with the physician and/or principal investigator. * May maintain clinical trials management system; prepare reports as needed. * May prepare for and conduct study monitor visits and audits. * Serves as liaison and reference to physicians, investigators and other staff members for questions regarding the research process. * Collaborates with investigator and regulatory staff regarding Institutional Review Board requirements. * May participate in protocol design, development, and writing, as well as writing study manuscripts. May complete scientific literature searches and due diligence practices prior to study inception. * Prepares basic statistical reports or other reports and presentations as required. * Collaborates with external community, business and academic partners. * Mentor research staff by acting as a content expert. * Perform other duties and responsibilities as assigned. Qualifications: * Education: Bachelor's degree. * Experience: 3 year's experience. * Licenses/Certifications: Current Basic Life Support (BLS) Provider Certified through American Safety and Health Institute, American Heart Association, or American Red Cross.
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