Job Overview
We are seeking a dynamic and detail-oriented Clinical Research Coordinator / Phlebotomist to join our innovative research team. In this pivotal role, you will oversee the planning, execution, and management of clinical trials and research projects, ensuring compliance with regulatory standards and scientific protocols. In this energetic position, you will be responsible for collecting blood samples and other specimens with precision and compassion, ensuring accurate processing and documentation. Your leadership will drive the success of research initiatives aimed at advancing medical knowledge and improving patient outcomes. This position offers an exciting opportunity to work at the forefront of clinical research, coordinating multidisciplinary teams, managing data collection processes, and ensuring adherence to Good Clinical Practice (GCP) guidelines. If you thrive in a fast-paced environment and are passionate about scientific discovery, this role is perfect for you!
Responsibilities
- Coordinate all aspects of clinical trials from start-up through closeout, including site initiation, monitoring, and documentation management
- Supervise research staff and research teams to ensure efficient workflow and compliance with study protocols
- Oversee data collection, entry, validation, and analysis to maintain accuracy and integrity of research data
- Ensure all activities comply with FDA regulations, ICH GCP standards, and drug regulation requirements
- Manage research administration tasks such as protocol development, ethics submissions, and regulatory documentation
- Lead training sessions on Good Clinical Practice (GCP), research ethics, and regulatory requirements for team members
- Monitor study progress, troubleshoot issues, and implement corrective actions to maintain project timelines
- Facilitate communication between investigators, sponsors, regulatory bodies, and other stakeholders involved in clinical trials
- Maintain detailed records of research activities, adverse events, and compliance documentation in accordance with research project management best practices
- Perform venipuncture and blood sampling using aseptic technique to ensure specimen integrity
- Collect, process, label, and document biological specimens accurately according to protocol
Requirements
- Proven supervising experience in clinical or scientific research settings with a track record of leading research teams effectively
- Strong background in clinical research procedures, including clinical trials management and data collection techniques
- Laboratory experience preferred to understand sample handling and experimental protocols
- Knowledge of FDA regulations, ICH GCP guidelines, drug regulation processes, and compliance management systems
- Experience with research administration tasks such as protocol writing, ethics submissions, and regulatory documentation preparation
- Skills in statistical analysis for research to interpret data accurately and support findings
- Valid ICH GCP certification from a recognized issuer for California or equivalent jurisdiction is highly desirable
- Demonstrated leadership abilities with excellent project management skills to oversee multiple research projects simultaneously
- Familiarity with research development project management tools and techniques
- Strong organizational skills with attention to detail in maintaining accurate records and ensuring regulatory compliance
- Certified or trained in phlebotomy with demonstrated venipuncture skills (blood sampling)
Join us to be part of a passionate team dedicated to pioneering medical advancements! This paid position offers an engaging environment where your expertise will directly contribute to impactful health solutions. We value innovation, integrity, and collaboration—qualities that drive our success in advancing scientific discovery.
Pay: $16.00 - $21.00 per hour
Experience:
- Clinical Research: 2 years (Required)
Language:
- English (Required)
- Spanish (Required)
License/Certification:
- Certified Phlebotomy Technician (CPT) (Required)
- GCP Certification (Required)
- IATA Certification (Required)
Work Location: In person
