Clinical Research Coordinator 5

Avispa MedOps; Palo Alto (CA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

W2 Employment, Group Medical, Dental,

Job summary

Avispa MedOps is seeking a Clinical Research Coordinator 5 to support thoracic clinical studies at a leading university site in Stanford, CA. The assignment is onsite, 40 hours per week, for six months with an hourly pay rate of $40.

The role involves coordinating from start-up through closeout, liaising with participants, sponsors, and regulators, and ensuring compliance with protocols and regulatory requirements.

Qualifications

• 2 years of related work experience or an equivalent combination of education and experience.
• Proficiency with Microsoft Office and basic data management tools.
• Knowledge of medical terminology.

Responsibilities

• Coordinate thoracic clinical studies from start-up through closeout.
• Serve as primary contact with participants, sponsors, and regulatory agencies.
• Determine participant eligibility and obtain consent; assist in recruitment strategies.

Skills

Microsoft Office

Medical terminology

Education

Bachelor's degree in a related field

Two-year college degree

Tools

Microsoft Office

Job description

Clinical Research Coordinator 5 1521189

• Hourly pay: $40/hr
• Worksite: Leading university (Stanford, CA 94305 - Onsite)
• W2 Employment, Group Medical, Dental, Vision, Life, Retirement Savings Program, PSL
• 40 hours/week, 6 Month Assignment

A leading university is seeking a Clinical Research Coordinator 5 to coordinate thoracic clinical studies from start-up through closeout.

Clinical Research Coordinator 5 Responsibilities:

• Serve as the primary contact with research participants, sponsors, and regulatory agencies, coordinating moderately complex aspects of one or more clinical studies from start-up through closeout, and participate in sponsor monitoring meetings, monitor visits, and regulatory audits.
• Determine participant eligibility and gather consent according to protocol, assist in developing recruitment strategies, and coordinate the collection and processing of study specimens.
• Collect and manage patient and laboratory data, manage research project databases, develop flow sheets and other study documents, complete case report forms, and ensure patient and research data are documented in appropriate files per institutional and regulatory requirements.
• Ensure compliance with research protocols by reviewing and auditing case report forms against source documents, preparing regulatory submissions, and completing Institutional Review Board renewals. Interact regularly with the principal investigator to ensure patient safety and proper study conduct.
• Assemble study kits for study visits, monitor the scheduling of procedures and charges, coordinate documents, monitor expenditures and adherence to study budgets, and resolve billing issues in collaboration with finance and management staff.

Clinical Research Coordinator 5 Qualifications:

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