Clinical Research Coordinator

Flourish Research•Walnut Creek, CA

23d•$26 - $34•Onsite

About The Position

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.

Requirements

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

Nice To Haves

Experience in diabetes trials (Type 1 & 2) is a plus.
Phlebotomy license and lab experience a plus, but not essential as we have a FT lab specialist on staff.

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.