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Sr. Lead Clinical Research Associate

Company: Disability Solutions
Location: Irvine
Posted on: June 4, 2024

Job Description:

Johnson & Johnson Vision Care, Inc., a member of Johnson & Johnson's Family of Companies, is recruiting for a Senior Lead Clinical Research Associate located in Irvine, CA OR Jacksonville, FL. At Johnson & Johnson Vision , we have a bold ambition: to change the trajectory of eye health. That's why, through our operating companies, we've developed solutions for every stage of life-to help people see better, connect better and live better. We partner with eye care professionals to provide some of the world's leading products and technologies to address refractive error, cataracts, dry eye, and beyond. We are committed to using our reach and size for good, and strive to put quality eye care within reach of everyone, everywhere. Visit us at Follow @JNJVision on Twitter and Johnson & Johnson Vision on LinkedIn. Position Summary: Responsible for the design, planning, implementation, and overall direction of clinical research projects. He/she manages the strategic elements of study conduct, ensuring that operating procedures and company policies are followed. Adheres to environmental policy, procedures, and supports department environmental objectives. Essential Job Requirements: --- Plan, guide, and report on the conduct of human clinical research studies required to enter new products into the marketplace or to expand product claims, in compliance with state and federal regulations, industry standards and corporate policies. --- Effectively manage multiple clinical studies/sites to assure accurate and timely initiation, enrollment, conduct and completion for assigned clinical trials while providing moderate level study management support. --- Apply applicable Corporate and Divisional policies and procedures, guidelines, standards and regulations. --- Under the support of a Study Manager, contribute to study design, development, conduct and closure. --- Lead project teams, providing input relative to study design, risk analysis and, appropriate clinical consultation relative to therapeutic area. --- Create, review and/or revise key study documents, including but not limited to protocol, investigator brochures, informed consent document templates, monitoring plans, and annotated monitoring visit report templates. --- Identify and evaluate investigators and investigative sites for assigned clinical trials. --- Assist in the development, testing and training for key clinical trial information systems (e.g., electronic data capture systems or electronic trial master file systems). --- Develop and implement a clinical trial training plan for internal and external personnel, including CRAs, CRA Assistants, and investigative site personnel. --- Provide leadership, protocol and monitoring support to CRAs allocated to assigned clinical trials, including resolution of team member conflict and communication issues, with support from Regional Managers and others, as needed. --- Responsible for study start-up activities including managing essential trial documents. --- Review and approve completed monitoring visit reports. --- Review study results, and contributing to final reports. --- Serve as primary contact for investigative site communication for each assigned site. --- Collaborate with investigative sites to ensure completion and appropriate submission of all required clinical trial documents prior to site initiation. --- Coordinate Institutional Review Board/ Ethics Committee (IRB/EC) approvals, as appropriate. --- Train investigative site personnel to ensure compliance with study requirements and GCP, including, but not limited to the protocol, IRB/EC instructions, industry guidelines, international standards and local and national regulations. --- Evaluate actual enrollment against assigned targets and working with assigned sites to meet, and whenever feasible, exceed enrollment targets. --- Assess eCRFs for trends in safety, effectiveness, and adherence to protocol. --- Manage study milestones and study metrics. --- Perform on-site monitoring activities for assigned investigative sites in compliance with the approved monitoring plan and SOPs, with specific tasks to include: o Ensuring that all clinical trial documentation is properly reviewed, approved and filed within the Trial Master File, and is accessible to investigative site personnel. o Ensuring investigational product and, as applicable clinical supplies accountability, handling and documentation are sufficient to continue, accurate, updated and appropriately delegated. --- Prepare, submit and file high quality monitoring visit reports and associated follow-up letters in a timely manner. --- Provide regular updates to the Investigator of assigned investigative sites, Study Manager and/or Lead CRA with respect to study conduct and compliance. --- Monitor overall progress of clinical trials by regularly attending project and/or clinical trial team meetings, reviewing team communications and sharing pertinent information with assigned investigative sites, Study Managers, Lead CRAs, CRAs and other clinical trial team members. --- Maintain audit/inspection readiness at assigned sites throughout the conduct and upon closure of clinical trials at assigned investigative sites. --- Ensue all equipment/supplies provided to investigative sites is appropriately reported to Study Manager. --- Identify training needs, developing materials and conducting training on clinical, therapeutic and/or compliance topics. --- Maintain effective working relationships with affiliate teams and external vendors.

Keywords: Disability Solutions, Irvine , Sr. Lead Clinical Research Associate, Healthcare , Irvine, California

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