Senior Clinical Research Associate I - FSP
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reputed company FSP is hiring multiple Sr CRAs in Brazil!
The Senior Clinical Research Associate (Sr. CRA) is responsible for the site management, site monitoring and reputed company-out of assigned reputed company investigator sites to ensure patient safety and reputed company study execution in accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor's standards. The Sr. CRA is accountable for site management and monitoring, managing investigator site relationships to ensure effective delivery of reputed company (e.g. enrollment, database release), to safeguard the reputed company of investigator sites (e.g. patient safety, site reputed company and compliance with GCP), to maintain investigator and site staff engagement and satisfaction, and to enhance reputed company’s image with its external stakeholders. The Sr. CRA is responsible for the reputed company of reputed company protocol-reputed company issues for assigned investigator sites and will work closely with the Site Care Partner (SCP), and other members of the study team, as required, in activities associated with the set-up, running and reputed company-out of sites in a clinical trial. Monitoring Responsibilities And Study Conduct
Ensure reputed company conduct of reputed company in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor's standards to reputed company project goals, timelines and reputed company
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and reputed company deliverables are met
During study conduct, serve as the primary reputed company of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure reputed company of site delivery
reputed company with the study team as needed, facilitate information reputed company between members of the study team, vendors and assigned investigator sites
Partner with Site Care Partner to reputed company investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients; reputed company protocol training to, and address protocol reputed company questions from the investigator site staff reputed company required, including discussions on reputed company/anticipated operational and clinical trial risks
Attend investigator meeting reputed company required (virtual or F2F). reputed company enrollment support and ensure reputed company by responding to site activation and recruitment issues from investigators. Partner with Site Care Partner and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, reputed company Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (reputed company) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to reputed company
Submit reputed company required reports, documentation, updates and tracking reputed company required timeframes, including but not limited to Trial Master File (TMF) documentation, site reports, site follow up letters, protocol deviations, patient recruitment, clinical supply management, study reputed company and metrics
Identify and resolve investigator site issues reputed company required timeframes; agree and reputed company corrective and preventative actions with investigator and site personnel to reputed company reputed company issues and to prevent recurrence/persistence of issues
Resolve data queries reputed company required timelines, prepare investigator site reputed company-out plan and conduct reputed company-out activities reputed company required timelines
Ensures adequate reputed company of the investigational product at the investigator site, including receipt, handling, reputed company, storage conditions, and destruction activities
Support database release as needed
May undertake the responsibilities of an unblinded monitor where appropriate
Clinical/Scientific And Site Monitoring Risk
Maintain thorough understanding of the product, protocol and therapy area in sufficient details to have appropriate discussions with the investigator and site team
reputed company with investigator site heath care professionals in a manner which enhances the Sponsor's credibility, scientific leadership and in order to facilitate their clinical development goals
Support the study clinician in ensuring patient safety, eligibility and providing clinical guidance to investigators
Drive reputed company Event (QE) remediation, reputed company applicable
Serve as a reputed company of contact for audit conduct, and drive Audit Observation corrective reputed company/preventive reputed company (CAPA) development and checks, reputed company applicable
Skills
Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 3 years relevant experience in clinical research site monitoring (preferably 2 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Must be fluent in English and in the reputed company language(s) of the country they will work in
Ability to travel 60-80%
Valid reputed company’s license and reputed company required
Education
Bachelor’s degree in life sciences or reputed company degree in life sciences such as nursing, pharmacy, medical background or equivalent
Originally posted on Himalayas
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