Onsite Clinical Research Coordinator — Oncology Trials

ALOIS Solutions; Palo Alto (CA); In loco; USD 100.000 - 167.000; Tempo pieno

Descrizione del lavoro

ALOIS Solutions in Palo Alto, CA seeks an onsite Clinical Research Coordinator for a 6-month contract with potential extension. You will independently manage key aspects of oncology and treatment trials, ensuring data integrity and regulatory compliance.

Responsibilities include data management, protocol adherence, IRB coordination, and collaboration with principal investigators and sponsors. The role requires a Bachelor’s degree in a related field and two years of clinical research experience.

Competenze

• Bachelor's degree in a related field and two years of experience in clinical research, or an equivalent combination of education and relevant experience.
• Experience with research protocols and regulatory or governing bodies, including HIPAA and FDA regulations, IRB requirements, and Good Clinical Practices.
• Knowledge of medical terminology.

Mansioni

• Conduct clinical research and independently manage progressively complex projects or studies.
• Oversee data management: organize, collect, report, and monitor data collection; extract, analyze, and interpret data.
• Audit operations and laboratory procedures to ensure regulatory compliance; monitor IRB submissions and respond to requests.
• Collaborate with principal investigators and study sponsors; monitor and report serious adverse events, resolve study queries.

Conoscenze

Medical terminology

Onsite coordination

Clinical research

Regulatory knowledge

Formazione

Bachelor's degree in a related field

Descrizione del lavoro

ALOIS Solutions in Palo Alto, CA seeks an onsite Clinical Research Coordinator for a 6-month contract with potential extension. You will independently manage key aspects of oncology and treatment trials, ensuring data integrity and regulatory compliance.

Responsibilities include data management, protocol adherence, IRB coordination, and collaboration with principal investigators and sponsors. The role requires a Bachelor’s degree in a related field and two years of clinical research experience.