Clinical Research Coordinator
Flourish Research, Walnut Creek, CA, United States
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 have an opening for a
Clinical Research Coordinator I/II
at our research site in Walnut Creek, CA! The Flourish Research Walnut Creek site, formerly known as Diablo Clinical Research in Walnut Creek, has proudly served the East Bay community for 30 years as a dedicated clinical research facility conducting Phase 1‑3 trials with major pharmaceutical sponsors and biotech innovators.
The Clinical Research Coordinator (CRC) serves as the main point of contact for study participants and Sponsor/CRO representatives. You'll work closely with investigators to ensure participant safety and accurate, timely data collection. Coordinators typically see 3‑5 patients daily, with higher volumes during high‑enrollment studies. Experience in diabetes trials (Type 1 & 2) is a plus. We’re actively enrolling for large‑scale vaccine studies and healthy volunteer device trials, including single‑visit and overnight stays.
Shift:
Monday‑Friday, 8:30 AM – 5:00 PM
Location:
2255 Ygnacio Valley Road, Suite M, Walnut Creek, CA 94598
Compensation:
$26/hr – $34/hr (depending on experience)
Benefits:
Health, dental, and vision insurance plans; 401(k) with a 100% employer match on the first 4% of employee contributions; tuition reimbursement; parental leave; referral program; employee assistance program; life insurance; disability insurance; and 15 days of PTO + 8 paid holidays and 2 floating holidays.
Responsibilities
Obtaining informed consent per ICH/GCP and site SOPs.
Reviewing and revising source documents and interviewing and collecting data from study participants.
Participating in protocol training meetings and completing online training for protocol‑specific software programs.
Dispensing/collecting study medication and providing accurate Investigational Product accountability.
Working with our lab specialist to obtain study participant laboratory specimens according to protocol (phlebotomy license and lab experience a plus, but not essential as we have a FT lab specialist on staff).
Completing study participant tracking information (either electronic or manual) accurately and on a timely basis. Responding and resolving data queries in a prompt manner.
Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
Performing basic data manipulation.
Maintaining a thorough understanding of all assigned clinical trial protocols.
Other duties as assigned.
Qualifications
Work experience as a CRC, preferably with a research site.
Bachelor's degree preferred.
Phlebotomy and EKG experience preferred.
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.
#J-18808-Ljbffr
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 have an opening for a
Clinical Research Coordinator I/II
at our research site in Walnut Creek, CA! The Flourish Research Walnut Creek site, formerly known as Diablo Clinical Research in Walnut Creek, has proudly served the East Bay community for 30 years as a dedicated clinical research facility conducting Phase 1‑3 trials with major pharmaceutical sponsors and biotech innovators.
The Clinical Research Coordinator (CRC) serves as the main point of contact for study participants and Sponsor/CRO representatives. You'll work closely with investigators to ensure participant safety and accurate, timely data collection. Coordinators typically see 3‑5 patients daily, with higher volumes during high‑enrollment studies. Experience in diabetes trials (Type 1 & 2) is a plus. We’re actively enrolling for large‑scale vaccine studies and healthy volunteer device trials, including single‑visit and overnight stays.
Shift:
Monday‑Friday, 8:30 AM – 5:00 PM
Location:
2255 Ygnacio Valley Road, Suite M, Walnut Creek, CA 94598
Compensation:
$26/hr – $34/hr (depending on experience)
Benefits:
Health, dental, and vision insurance plans; 401(k) with a 100% employer match on the first 4% of employee contributions; tuition reimbursement; parental leave; referral program; employee assistance program; life insurance; disability insurance; and 15 days of PTO + 8 paid holidays and 2 floating holidays.
Responsibilities
Obtaining informed consent per ICH/GCP and site SOPs.
Reviewing and revising source documents and interviewing and collecting data from study participants.
Participating in protocol training meetings and completing online training for protocol‑specific software programs.
Dispensing/collecting study medication and providing accurate Investigational Product accountability.
Working with our lab specialist to obtain study participant laboratory specimens according to protocol (phlebotomy license and lab experience a plus, but not essential as we have a FT lab specialist on staff).
Completing study participant tracking information (either electronic or manual) accurately and on a timely basis. Responding and resolving data queries in a prompt manner.
Maintaining a thorough understanding of all data collection instruments and collecting data accurately and according to protocol.
Performing basic data manipulation.
Maintaining a thorough understanding of all assigned clinical trial protocols.
Other duties as assigned.
Qualifications
Work experience as a CRC, preferably with a research site.
Bachelor's degree preferred.
Phlebotomy and EKG experience preferred.
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.
#J-18808-Ljbffr