Clinical Research Coordinator Associate — On-Site Trials Lead

SLAC; Palo Alto (CA); Vor Ort; USD 60.000 - 112.000; Vollzeit

Benefits dieser Stelle

Health benefits

PTO 18+ days

Flexible work options

Tuition assistance

403(b) plan

Zusammenfassung

Stanford University in Stanford, CA, seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions. This on-site role works with the Stanford Hospital and Clinics, coordinating visits, data collection, and adverse event reporting under GCP and HIPAA guidelines.

Qualifications include a two-year degree with experience or a related bachelor's, proficiency in MS Office, and knowledge of medical terminology.

Qualifikationen

• Two-year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.
• Proficiency with Microsoft Office.
• Knowledge of medical terminology.

Aufgaben

• Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
• Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
• Coordinate collection of study specimens and processing.
• Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
• Ensure compliance with research protocols, and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed.
• Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.

Kenntnisse

Interpersonal skills

Microsoft Office

Medical terminology

Ausbildung

Two-year college degree or equivalent with related experience

Jobbeschreibung

Stanford University in Stanford, CA, seeks a Clinical Research Coordinator Associate to manage multiple protocols, ensure regulatory compliance, and support IRB submissions. This on-site role works with the Stanford Hospital and Clinics, coordinating visits, data collection, and adverse event reporting under GCP and HIPAA guidelines.

Qualifications include a two-year degree with experience or a related bachelor's, proficiency in MS Office, and knowledge of medical terminology.