Clinical Research Coordinator (Medical Assistant/Phlebotomy) jobs-in Huntington Beach,CA,US

ed and highly organized Clinical Research Coordinator (CRC) to support and manage day-to-day activities related to clinical trials and research studies. This role is responsible for ensuring protocol compliance, participant coordination, regulatory documentation, specimen handling, and communication with sponsors and regulatory bodies.

Candidates with Phlebotomy or Medical Assistant (MA) certification are strongly preferred, as the role may include specimen collection and basic clinical procedures.
Key Responsibilities
• Coordinate and oversee daily operations of clinical research studies in accordance with study protocols and regulatory requirements
• Recruit, pre-screen, consent, and enroll eligible study participants
• Conduct participant visits and ensure all assessments are completed within protocol-defined timelines
• Collect, process, label, and ship biological specimens (e.g., blood, urine) per study guidelines
• Perform basic clinical procedures aligned with certification, including vital signs and EKGs
• Maintain accurate, complete, and timely documentation in electronic and paper case report forms (CRFs)
• Communicate effectively with study sponsors, monitors, and Institutional Review Boards (IRBs) regarding study progress and compliance
• Assist with preparation, maintenance, and submission of regulatory documents and IRB materials
• Maintain investigational product accountability and ensure proper storage and handling when applicable
• Schedule study visits, manage participant follow-ups, and track study timelines
• Ensure adherence to Good Clinical Practice (GCP), SOPs, and regulatory standards

Qualifications
• Bachelor's degree in a health-related field or equivalent clinical research experience
• 1-2 years of clinical research experience preferred
• Phlebotomy Certification or Medical Assistant (MA) Certification preferred
• Strong knowledge of Good Clinical Practice (GCP) and clinical research regulations
• Excellent organizational skills with strong attention to detail
• Effective communication and interpersonal skills
• Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms)
• Ability to work independently and collaboratively in a multidisciplinary team environment

Preferred Qualifications
• Prior experience in clinical trials within a hospital, academic, or research center setting
• Familiarity with IRB processes and regulatory documentation
• Bilingual skills are a plus, depending on patient population

If you're interested or want more details, feel free to call me at 469-290-8978or email me at [email protected]. Looking forward to connecting!