On-Site Clinical Research Coordinator II

Stanfordlivetickets; Palo Alto (CA); On-site; USD 76,000 - 142,000; Full time

Benefits offered by this job

18+ PTO days per year

Health benefits start when you start

Flexible work options

Tuition and training assistance ($6000

403(b) plan

Mental health programs

Commuter transportation benefits

Job summary

Stanford is seeking a Clinical Research Coordinator 2 to work on-site in Stanford, CA. The role manages recruitment, study start-up activities, data management, and regulatory compliance across trials in collaboration with multiple departments and the CHRI.

The candidate should have a bachelor's degree in a related field with at least two years of clinical research experience, strong organizational skills, and proficiency in Microsoft Office and databases. IRB processes and GCP may be involved.

Qualifications

• Bachelor's degree in a related field and two years of clinical research experience, or an equivalent combination.
• Experience with university research policies and procedures.
• Knowledge of medical terminology and regulatory requirements.

Responsibilities

• Oversee subject recruitment and study enrollment goals.
• Develop project schedules, targets, and accountabilities; lead team meetings.
• Audit operations to ensure regulatory compliance and quality.
• Collaborate with principal investigators and study sponsors; monitor adverse events.
• Maintain study documentation and ensure regulatory compliance.

Skills

University research policies

Organizational skills

Independent work capability

Prioritization

Communication skills

Problem solving

CV experience

Interpersonal skills

Microsoft Office proficiency

Database applications proficiency

HIPAA and FDA regulations knowledge

Education

Bachelor's degree in a related field

Two years of clinical research experience

Job description

Stanford is seeking a Clinical Research Coordinator 2 to work on-site in Stanford, CA. The role manages recruitment, study start-up activities, data management, and regulatory compliance across trials in collaboration with multiple departments and the CHRI.

The candidate should have a bachelor's degree in a related field with at least two years of clinical research experience, strong organizational skills, and proficiency in Microsoft Office and databases. IRB processes and GCP may be involved.