Flourish Research
Senior Clinical Research Coordinator
Flourish Research, Southfield, Michigan, United States, 48076
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 Senior Clinical Research Coordinators at our Detroit, MI location! The Senior 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, 9 AM - 5 PM; one Saturday each month (9 AM - 1 PM)
Location:
20755 Greenfield Rd # 107, Southfield, MI 48075
Compensation:
$30 - $36 based on experience + quarterly discretionary performance bonuses
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.
Communicates with the Study Sponsor/CRO regarding study‑specific questions.
Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.
Additional duties as assigned by management.
Qualifications
Bachelor's degree preferred but not required.
Phlebotomy experience is required; EKG or other patient labs/processes preferred.
5+ 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.
It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status.
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!
#J-18808-Ljbffr
We are actively hiring Senior Clinical Research Coordinators at our Detroit, MI location! The Senior 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, 9 AM - 5 PM; one Saturday each month (9 AM - 1 PM)
Location:
20755 Greenfield Rd # 107, Southfield, MI 48075
Compensation:
$30 - $36 based on experience + quarterly discretionary performance bonuses
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.
Communicates with the Study Sponsor/CRO regarding study‑specific questions.
Participates in site visits from Sponsors/CROs, including site initiation and monitoring visits.
Additional duties as assigned by management.
Qualifications
Bachelor's degree preferred but not required.
Phlebotomy experience is required; EKG or other patient labs/processes preferred.
5+ 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.
It is the policy of Flourish Research not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, or veteran status.
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!
#J-18808-Ljbffr