Senior Clinical Research Associate

Integrated Resources, Inc ( IRI ) provided pay range

This range is provided by Integrated Resources, Inc ( IRI ). Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

$65.00/hr - $66.00/hr

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Job Title: Clinical Trials Management Associate - III

Location: Considering local candidates to any of the west coast sites:
Santa Monica, El

Job Duration: 12+ Months (Possibility of Extension)

NOTE: Working mostly remote but subject to change to comply with policy.

• 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 supervisors, coordinate 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 run 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, participate in two or more departmental or interdepartmental strategic initiatives.
• Travel is 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 the measured efficiency 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).
• CCRA or other certifications desired.

Mid-Senior level

Contract

Science, Research, and Other

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing

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