Job Title : Clinical Research Associate
Contract Duration : 6 Months
Pay range : $70 - 85 / hr
Location : Boston, MA
Work Type : Hybrid
Job Description :
- The primary responsibility of the Clinical Research Associate is to conduct site monitoring visits in accordance with CTNI's SOPs, ICH GCP guidelines, and federal regulations to ensure that
the rights and well-being of human subjects are protected and
electronic case report forms (e-CRF) are accurate, complete, and verifiable from source documents.Primary Duties :
Responsible for conducting study monitoring visits (Site Qualification Visit to Close Out Visit) to assess protocol and regulatory compliance per the approved monitoring plan.Review and compare source documentation to eCRFs to ensure data is complete and accurate.Clinical Research Associate provides Investigator and study staff training at study initiation and as needed through the course of the trial.Review study-specific site documents including regulatory documents, drug accountability logs, training logs, the delegation of authority logsMaintain regular communication with assigned sites to support site enrollment, data entry, query resolution, and patient retention.Document site visit findings and observations via trip reports and letters.Escalate major visit findings as described in the monitoring plan to appropriate study team members.Participate in weekly meetings with the study team.Other Tasks, as required :
Participate in the site and / or investigator identification, evaluation, and selection processes.Attend and participate in investigator and coordinator meetings, as needed.Submit monitoring visit expense reports in a timely manner.Assist with central monitoring and site management duties.Competencies Required :
Excellent oral and written communication skillsSound interpersonal skillsAbility to work independentlyAbility to travel up to 50% of the timeAbility to identify problems and develop solutionsExceptional attention to detailAbility to navigate and utilize multiple online systems and softwareRequired Education and Experience :
BA or BS in a life sciences-related field or registered nursing certificateMinimum of 3 years monitoring experiencePain research experience is a plusMust be knowledgeable of clinical trial systems and Microsoft Office applicationsMust have the capability to complete primary duties for multiple studiesExpectations for All Employees :
Supports the organization's missions, vision, and values by exhibiting the following behaviors; excellence and competence, collaboration, innovation, respect, personalization, commitment to our community, and accountability and ownershipBenefits :
Medical, Vision, and Dental Insurance Plans401k Retirement FundAbout GTT :
GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. As a Native American-owned, economically disadvantaged corporation, we highly value diverse and inclusive workplaces. Our clients are Fortune 500 banking, insurance, financial services, and technology companies, along with some of the nation's largest life sciences, biotech, utility, and retail companies across the US and Canada. We look forward to helping you land your next great career opportunity!
25-18311 : #LI-GTT #gttjobs #LI-Hybrid
Salary : $70 - $85
