Senior Clinical Research Associate
- Expired: over a month ago. Applications are no longer accepted.
Job Title: Senior Clinical Research Associate
Location: Boston, MA (Remote/Home Based with Regional New England travel)
Duration: 12 month renewable contract
Compensation: Salaried + benefits
Excellent opportunity for a Senior CRA on a long term contract basis working in a fully embedded model for a large sponsor client.
- Educational requirement: BA/BS
- Years of experience: 2+ years of CRA (monitoring experience) - Ideally 5 years of field CRA experience
- Industry experience: 5+ years of clinical research industry experience
- Diabetes experience is a nice to have
- Remote Monitoring Experience
- Risk Based Monitoring
KEY AREAS OF RESPONSIBILITY
Responsible for providing site management and support to external trial staff (Principal Investigators and Study Coordinators) from trial initiation to closeout
Ensure collection of high quality data, timely adverse event reporting, subject protection and compliance to the protocol
Adherence to ICH-GCP, regulatory requirements, local ethics requirements, Company SOPs, and Clinical Development Guidelines
Manage recruitment and retention strategies at the site level, analyzing enrollment and randomization projections against actual recruitment numbers to ensure targets are met
Collaborates regularly with Local Trial Manager (LTM) and Line of Business Manager, communicating site progress and escalating critical issues that could impact trial milestones
Trains and supports external trial staff regarding requirements for CRF and IVRS data entry, AE/SAE/MESI reporting, ethics reporting, protocol deviation identification, drug accountability and temperature monitoring, query resolution, essential document collection and ITF filing
Identifies objectives for scheduled monitoring visits; ensures planned visit objectives are achieved to meet protocol and SOP timelines.
Prepares and completes monitoring visit reports and follow up letters within the timeline established by the applicable SOPs and guidelines
Completes system training (IMPACT, IV/WRS, EDC, CATS, CONCUR etc.) in order to adhere to protocol and SOP timelines to meet required deliverables.
Proactive use of EDC and other data source systems for preparation and conduct of site visits as well as source data verification in collaboration with data management/logistics team
Identify potential risks and proactively take action to prevent or mitigate
Participates in Sponsor and Regulatory audits in Canada; preparing external trial staff and site records, addressing questions from Auditor, supporting external trial staff during audit, preparing audit responses ensuring compliance to local guidelines, Company SOPs and ICH-GCP.
Adheres to Company policies, procedures ,vision and fundamentals
Acts as back up to the other monitors during absences, as requested
Performs other tasks as assigned by management
Works from a home office 2-3 days per week
Works at hospitals, medical clinics 2-3 days per week
May be required to drive, fly or take train to location to perform duties of the job
Up to 70% travel required
JouleWhy Work Here?
Amazing Clinical Research position for RN's and LPN's. Amazing benefits and stock options.
At Joulé, we believe our world is filled with possibilities – where character, integrity, and commitment drive our purpose. For over 30 years, Joulé has been a trusted partner to industry leading clinical, scientific, and healthcare organizations by providing innovative workforce solutions and delivering top talent. Operating at the forefront of the life sciences arena, Joulé’s relentless approach enables our clients to rapidly and effectively execute critical initiatives and major projects. Joulé is a System One division.