About Us:
Flourish Research is where clinical trials thrive. Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. At Flourish Research, we strive toward excellence. In clinical trials and healthcare, excellence means everyone deserves the best care, regardless of their race, color, gender identity, religion, ethnicity, physical abilities, age, sexual orientation, or veteran status. We embrace employees, customers, and patients from these underrepresented groups to help make this vision a reality. Flourish is committed to a safe work environment where all employees, customers, and patients are included, and treated with dignity and respect. The more diversity we have in our team, the more unique perspectives, and ideas we share, and the better prepared we are to serve our communities. WE SEE YOU. WE ARE YOU. WE EMBRACE YOU. WE CELEBRATE YOU!
Flourish Research is looking for motivated, talented, creative individuals who want to learn and grow in their careers while contributing to research that changes lives! We offer an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.
About the Job:
We are actively hiring a Sr. Clinical Research Coordinator to support our Covina, California site.
Shift: Monday-Friday day shift (40 hours per week)
Location: Onsite, Covina, CA
FLSA Classification: Non-Exempt
Compensation : $32 to $38 per hour (depending on experience)
PURPOSE: To coordinate a variety of complex activities and perform duties and procedures related to the start-up, conduct and close-out phases of clinical pharmaceutical and device research protocols. To obtain clean, objective, and accurate data within sponsor timelines while following applicable Flourish SOPs, policies and procedures, federal regulations, medical ethics, Good Clinical Practices (GCPs), International Council of Harmonization (ICH), Institutional Review Board (IRB) requirements, and in compliance with specific sponsor protocol requirements. All responsibilities should be completed in accordance with Flourish Research’s Core Values, Mission Statement and Employee Manual.
ESSENTIAL JOB FUNCTIONS:
· Read, understand, and accomplish protocol specified patient visits and procedures.
· Clearly and concisely document patient assessments, observations, test results and other study related information per federal regulations, protocol requirements and GCPs.
· Obtain patient informed consent according to federal regulations, GCPs and IRB requirements.
· Is creative and diligent in recruiting qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsor’s timeline while following regulations and rules governing medical ethics, IRB, GCP and ICH guidelines.
· Complete all required training in a timely manner.
· Schedule and conduct patient visits according to protocol requirements and timelines.
· Maintain accurate and complete written source documentation of patient visits and protocol related activities.
· Accurately complete case report forms (CRFs &/or eCRFs) and/or worksheets generated by the sponsor.
· Maintain confidentiality of patient and protocol issues as appropriate and as bound by Confidentiality.
· Agreements with Flourish Research, between Flourish and sponsors, and between Flourish and other entities, as well as HIPAA regulations.
· Promptly report adverse events to supervisor and/or Principal Investigator/Sub-Investigator as deemed necessary.
· Report Serious Adverse Events (SAEs) to sponsor within 24 hours of becoming aware of the SAE.
· Also report the SAE to the supervisor, Principal Investigator and/or Sub-Investigator.
· Account for clinical trial materials (i.e., CRFs, study drug, lab supplies, and/or other required items).
· and ensure availability of appropriate…