Clinical Research Coordinator

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.

We are actively hiring Clinical Research Coordinator at our Keystone Clinical Studies site in Plymouth Meeting, PA!

The Clinical Research Coordinator assists the Investigators in executing Phase I, II, III, and IV clinical research trials in accordance with Standard Operating Procedures (SOPs), FDA and GCP guidelines, and study protocols while providing an impeccable patient experience in every, single interaction.

Shift :

• Monday-Friday, 8 : 30 AM - 5 PM (occasional weekends) Compensation :   Hourly Rate based on experience Benefits :   Health, dental, and vision insurance plans, 401k with 4% match, tuition reimbursement, parental leave, referral program, employee assistance program, life insurance, disability insurance, and 15 days of PTO + 10 company holidays.  RESPONSIBILITIES The Clinical Research Coordinator (CRC) obtains study participant informed consent.
• Executes study protocol procedures in a detailed, organized, and professional manner.
• Performs human specimen lab draws and processing, and packages specimen shipments.
• Creates and completes study source documents and adverse event reporting on an e-source system.
• Maintains study-specific files and supplies.
• Communicate with the Study Sponsor / CRO regarding study-specific questions.
• Participates in site visits from Sponsors / CROs, including site initiation and monitoring visits.
• QUALIFICATIONS Bachelor's degree preferred, but not required Experience working neurology studies is a plus, but not required - this site primarily conducts Alzheimer's clinical studies Phlebotomy experience is required, EKG or other patient labs / processes preferred Preferably 2+ years of experience as a Clinical Research Coordinator Familiar with e-source reporting via an electronic platform A clear understanding of ICH, FDA, and GCP regulations Impeccable organizational skills and attention to detail Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor / CROs, potential subjects, and referral sources An ethical compass that compels the candidate to be honest, detail-oriented, and self-driven High-level critical thinking skills Working knowledge of medical terminology and lab collection / processing / storage procedures Proficiency with computers and Microsoft Office Suite Flourish Research offers an excellent comprehensive benefits package, a supportive and collaborative work environment, and endless growth opportunities.

Apply today to learn more about how you can join us in our mission to save and improve the lives of others!