Title: Clinical Research Associate 
Location: Remote - 50% travel 
Type: Contract

Responsibilities: 

• Develops strong investigative site relationships and ensures continuity of investigative site relationships through all phases of the trial (will be performing on site monitoring and remote monitoring)
• Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations
• Performs remote and on-site monitoring & oversight activities using various tools to ensure data generated at the site are complete, accurate, and unbiased; subjects' rights, safety, and well-being are protected
• Collects, reviews, and monitors required regulatory documents for study start-up, study maintenance, and study close-out
• Communicates with Investigators and site staff on issues related to protocol conduct, recruitment, retention, missing data and data queries, protocol deviations, regulatory documentation, site audits/inspections, and overall site performance
• Identifies, assesses, and resolves site performance, quality, or compliance problems and escalates per protocol to upper management
• Performs investigational product accountability through physical inventory and record review
• Participates & provides inputs on site selection activities
• Supports audit/inspection activities as needed
• Work with in-house Clinical Trial Assistant to collect, review, and monitor required regulatory documentation for study start-up, study maintenance, and study close-out.

Requirements:

• Bachelor's degree in Sciences from an accredited institution with strong emphasis in science and/or biology
• Minimum of 2-3 years of direct site management experience in a bio/pharma/ Clinical Research Organization
• Minimum of 1-3 years of clinical monitoring or direct site management experience in a bio/pharma/ Clinical Research Organization in the oncology space. Site level experience is required – knowledge of imaging, resistance (clinical trial coordination, study start up), and experience managing oncology trials at big academic centers
• Applicants may be eligible to work remotely depending on location
• Ability to travel domestically approximately 50% of working time
• Current driver's license preferred 
• COVID vaccination required