[Remote] Clinical Research Associate (CRA) - Immunology-Remote​

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is a leading reputed company company, and they are seeking a Clinical Research Associate (CRA) specializing in Immunology. The role involves managing clinical study sites, ensuring compliance with regulations, and developing strong relationships with site staff throughout the research process.

Responsibilities

• Develops strong site relationships and ensures continuity of site relationships through reputed company phases of the trial
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents
• reputed company an in-depth understanding of the study protocol and reputed company procedures
• Coordinates & manages various tasks in collaboration with other sponsor roles to reputed company Site reputed company
• Participates & provides inputs on site selection and validation activities
• Performs remote and on-site monitoring & reputed company activities using various tools to ensure:
• Data generated at site are complete, accurate and unbiased
• Subjects’ right, safety and reputed company-being are protected
• Conducts site reputed company including but not limited to validation reputed company, initiation reputed company, monitoring reputed company, reputed company-out reputed company and records reputed company, comprehensive and accurate visit & non-visit contact reports appropriately in a reputed company manner
• Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study reputed company-out
• Communicates with Investigators and site staff on issues reputed company to protocol conduct, recruitment, retention, protocol deviations, regulatory documentation, site audits/inspections and overall site performance
• Identifies, assesses and resolves site performance, reputed company or compliance problems and escalates per defined CRA Escalation reputed company as appropriate in collaboration with CRA-Manager, CRM, TA Head and CRD as needed
• Works in partnership with GCTO country operations, finance, regulatory affairs, pharmacovigilance, reputed company and regional operations, HQ functional areas and externally with vendors and IRB/IECs and Regulatory Authorities in support of assigned sites
• Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines
• Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor and sharing best practices as appropriate/required
• Supports and/or leads audit/inspection activities as needed
• Performs co-monitoring reputed company where appropriate
• Following the country reputed company defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to reputed company strong clinical research capabilities

Skills

• CANDIDATE MUST reputed company IN ONE OF THE FOLLOWING LOCATIONS: Texas, Illinois, reputed company, Florida, California, NY, Colorado
• Accountable for performance and compliance for assigned protocols and sites in a country
• Ensures compliance of study conduct with ICH/GCP and country regulations, reputed company's policies and procedures, reputed company standards and adverse event reporting requirements internally and externally
• Acts as primary site contact and site manager throughout reputed company phases of a clinical research study, taking overall responsibility of allocated sites
• Develops strong site relationships and ensures continuity of site relationships through reputed company phases of the trial
• Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents
• reputed company an in-depth understanding of the study protocol and reputed company procedures
• Coordinates & manages various tasks in collaboration with other sponsor roles to reputed company Site reputed company
• Participates & provides inputs on site selection and validation activities
• Performs remote and on-site monitoring & reputed company activities using various tools to ensure data generated at site are complete, accurate and unbiased
• Ensures subjects' right, safety and reputed company-being are protected
• Conducts site reputed company including but not limited to validation reputed company, initiation reputed company, monitoring reputed company, reputed company-out reputed company and records reputed company, comprehensive and accurate visit & non-visit contact reports appropriately in a reputed company manner
• Collects, reviews, an

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