Clinical Research Coordinator

2 days ago

San Francisco, California, United States SF Research Institute Full time

About SFRI

San Francisco Research Institute (SFRI) is a
global Clinical Research Institute

with over
25 years of experience

and more than
1,000 successfully completed studies

across biotechnology, pharmaceuticals, medical devices, dermatology, cosmetics, nutrition, and wellness. SFRI provides comprehensive clinical and regulatory support—from proof of concept to product launch—helping companies bring safe, effective, and scientifically validated innovations to market

Position: Clinical Research Coordinator

SFRI is seeking a
Clinical Research Coordinator

with hands-on experience managing studies at a private clinical site. The ideal candidate will have a strong background in coordinating studies related to
pharma (Oncology) and dietary supplements

, with a passion for advancing clinical evidence in wellness and aesthetics. This position offers an opportunity to work with innovative research protocols, cutting-edge skin assessment technologies, and a collaborative scientific team.

Key Responsibilities

  • Coordinate and manage all phases of clinical research studies—from initiation through closeout—ensuring full protocol compliance and operational excellence.
  • Lead and expand patient recruitment efforts across multiple channels to meet study enrollment goals.
  • Screen, consent, and enroll eligible participants according to study-specific inclusion and exclusion criteria.
  • Serve as the primary point of contact for sponsors, laboratories, and internal research staff to ensure smooth communication and study execution.
  • Collaborate with phlebotomists, coordinators, and laboratory teams to support sample collection, processing, and data accuracy.
  • Operate and maintain advanced skin research instruments, ensuring calibration and quality control in accordance with manufacturer and study specifications.
  • Collect vital signs and anthropometric data as required by study protocols, including blood pressure, temperature, heart rate, weight, height, and waist measurements.
  • Facilitate biological sample collection such as blood, urine, or stool when required, and ensure proper labeling, documentation, and shipment to certified laboratories.
  • Maintain detailed source documents, monitoring reports, participant visit logs, and regulatory documentation.
  • Ensure strict adherence to ICH-GCP and ethical standards throughout the conduct of all studies.

Qualifications

  • Bachelor's degree in life sciences, nursing, or a related health discipline.
  • Prior experience as a clinical research coordinator within a private site setting.
  • Familiarity with studies in personal care, skincare, or nutraceutical categories.
  • Strong interpersonal and organizational skills, with the ability to manage multiple studies concurrently.
  • Proficiency in maintaining accurate documentation, source data, and regulatory files.
  • Commitment to data integrity, patient safety, and scientific rigor.

Preferred Qualifications

  • Experience working with industry-sponsored trials or consumer health research.
  • Knowledge of skin assessment devices and imaging technologies.
  • Atleast 4 years of working full-time as a CRC in the U.S.
  • Phlebotomy certification or prior hands-on experience in sample collection.

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