Integrated Resources, Inc ( IRI ) · 5 days ago
Senior Clinical Research Associate
California, United States
Contract
Hybrid
Mid, Senior Level
$65/hr - $65/hr
4+ years expIntegrated Resources, Inc (IRI) is seeking a Senior Clinical Research Associate to conduct site evaluations and ensure compliance with protocols and regulations. The role involves coordinating with CROs and vendors, drafting study documents, and participating in the training of Clinical Research Associates.
BiotechnologyHealth CareHuman ResourcesRecruitingStaffing Agency
Hiring Manager
Sasha Sharma
Responsibilities
Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas
With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required
Assures site compliance with the routine protocol and regulatory requirements and quality of data
Assists in the setting and updating of study timelines
Assists in CRO or vendor selection
With guidance from supervisor coordinates CROs or vendors
Drafts and coordinates review of protocols, informed consents, case report forms and monitoring plans
Assists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies
Participate or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams (May participate in abstract presentations, oral presentations and manuscript development)
Interfaces with individuals in other functional areas to address routine study issues
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants
Under general supervision, participates in two or more departmental or interdepartmental strategic initiatives
Travel is required
Qualification
Required
Must meet all requirements for Clinical Research Associate position and have demonstrated proficiency in all relevant areas
With limited supervision conducts site evaluations/initiations and closeout visits in addition to routine monitoring visits, as required
Assures site compliance with the routine protocol and regulatory requirements and quality of data
Assists in the setting and updating of study timelines
Assists in CRO or vendor selection
With guidance from supervisor coordinates CROs or vendors
Drafts and coordinates review of protocols, informed consents, case report forms and monitoring plans
Assists in the review of routine data and preparation of safety, interim, and final study reports, and resolution of data discrepancies
Participate or effectively runs meetings and conference calls with CROs, vendors, and multi-functional teams (May participate in abstract presentations, oral presentations and manuscript development)
Interfaces with individuals in other functional areas to address routine study issues
May be asked to assist in the training of Clinical Research Associates and Clinical Project Assistants
Under general supervision, participates in two or more departmental or interdepartmental strategic initiatives
Travel is required
Excellent verbal, written, interpersonal and presentation skills are required
Working knowledge and experience with Word, PowerPoint and Excel
Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials
Must be able to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures
Ability to develop tools and processes that increase measured efficiencies of the project
Must be able to anticipate obstacles and proactively develop solutions to achieve project goals
Must have a general understanding of functional issues and routine project goals from an organizational perspective
4+ years of experience and a BS or BA in a relevant scientific discipline
4+ years of experience and an RN (2 or 3 year certificate)
Excellent verbal, written, interpersonal and presentation skills
Working knowledge and experience with Word, PowerPoint and Excel
Working knowledge of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of routine clinical trials
Ability to prioritize multiple tasks, plan proactively, and accomplish goals using well-defined instructions and procedures
Ability to develop tools and processes that increase measured efficiencies of the project
Ability to anticipate obstacles and proactively develop solutions to achieve project goals
Preferred
CCRA or other certification desired
Company
Integrated Resources, Inc ( IRI )
Integrated Resources Inc.
501-1000 employees
Funding
Current Stage
Late StageRecent News
2025-06-11
2025-06-11
2025-04-14
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