Irvine Clinical Research

Senior Clinical Research Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours

Full-time$85k - $100k /yrIn-person

About the Job

Requirements

Five or more years of industry-sponsored drug trial experience.
Demonstrated ability to work on high-enrolling Phase II/III clinical trials.
Ability to work accurately and quickly with a clinical trial management system (CTMS).
Command of professional spoken and written English.
Extensive experience with study start-up, trial execution, adverse event reporting, source creation and documentation, pharmacy and laboratory operations, and query resolution.
Clinical leadership capabilities to serve as an operations leader and train staff as needed.
Attention to detail and ability to handle multiple tasks with precision.

Responsibilities

Coordinate the day-to-day clinical operations of clinical research studies.
Perform study procedures in accordance with Good Clinical Practice (GCP) and study protocols.
Organize and maintain paper and electronic study data completely and correctly.
Work closely with recruitment and prescreening teams to meet study enrollment goals.
Conduct diagnostic, efficacy, and safety assessments as needed.
Mentor and lead less experienced coordinators and/or research assistants.
Take ownership of team productivity (enrollment) and quality metrics.
Own study start-up tasks, including vendor communication and qualification.

Salary Range: 85000 to 100000 (Currency: USD) (Pay period: per-year-salary)

Inglewood Clinical Research, a research site specializing in late phase CNS clinical trials, is seeking applicants for a Senior Clinical Research Coordinator with extensive clinical trial experience. The Senior CRC will work as a primary coordinator on Phase I-III clinical trials in Neurology, Psychiatry, and Cardiometabolic.

Candidates should have extensive experience with study start-up, trial execution, adverse event reporting, source creation and documentation, pharmacy and lab operations, as well as query resolutions. Candidates should also have clinical leadership capabilities to serve as an operations leader and train staff as needed.

Job Duties

Coordinate the day-to-day clinical operations of clinical research studies
Perform study procedures in accordance with GCP and study protocols
Organize and maintain paper and electronic study data in a complete and correct manner
Work closely with recruitment and prescreening teams to meet study enrollment goals
Conduct diagnostic, efficacy, and safety assessments as needed
Mentor and lead less experienced coordinators and/or research assistants
Take ownership of team productivity (enrollment) and quality metrics
Own study study start-up tasks, including vendor communication and qualification

Job Requirements

Five (5) or more years of industry-sponsored drug trial experience
Demonstrated ability to work on high-enrolling Phase II/III clinical trials
Attention to detail and the ability to handle multiple tasks with precision
Demonstrated ability to work accurately and quickly with CTMS
A command of professional spoken and written English

Equal Opportunity & Fair Chance Employer Irvine Clinical Research and its affiliates are Equal Opportunity Employers. We celebrate diversity and are committed to creating an inclusive environment for all employees.

About the Company

Irvine Clinical Research

Company size: Not listed
Company stage: Not listed
Total funding: Not listed
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