Description Job Title:

Clinical Research Coordinator 2 - GI team

Location Address:

Palo Alto, CA 94305 (Onsite 5 days per week) Duration of project (start and end date): ASAP to 6 months Full Time (40 hours per week) Shift timing/schedule: Day business hours Will the resource be working with minors? No How many years of experience are required? 1-2 years Will this role extend or possibly convert to an FTE?

Yes PR Range:

$44.82/hr. On W2 - $51.72/hr on W2 without benefits Top 3 requirements to hire? Experience in oncology clinical research Onsite coordinator work Treatment trials in phases 1-III

JOB PURPOSE

Perform duties related to the coordination of clinical studies. Coordinate moderately complex aspects of one or more clinical studies and work under the close direction of the principal investigator and/or study coordinator/supervisor.

CORE DUTIES

Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through closeout. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Coordinate the 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. Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff. Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct. Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements. Participate in monitoring visits and regulatory audits.

Education & Experience:

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.

Knowledge, Skills, and Abilities:

Strong interpersonal skills. Proficiency with Microsoft Office. Knowledge of medical terminology.

Certifications and Licenses:

Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.

PHYSICAL REQUIREMENTS

Frequently stand, walk, twist, bend, stoop, squat, and use fine light/fine grasping. Occasionally sit, reach above shoulders, perform desk-based computer tasks, use a telephone, and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds. Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more. Ability to drive day or night, if applicable.