Centricity Research

Clinical Research Coordinator I - LPN

Posted 30+ days ago

Job summary

  • Job post source

    This job is directly from Centricity Research

  • Job overview

    The Clinical Research Coordinator I - LPN at Centricity Research supports clinical studies by coordinating and managing study activities to ensure protocol compliance and participant safety.

  • Responsibilities and impact

    The role involves screening and enrolling study participants, conducting study visits including clinical assessments and sample collection, managing safety reporting, maintaining study documentation, and supporting recruitment and study operations.

Company overview

Centricity Research is a leading clinical research organization specializing in conducting Phase I-IV clinical trials across various therapeutic areas. They generate revenue by partnering with pharmaceutical, biotechnology, and medical device companies to facilitate the development and approval of new treatments. Founded with a mission to advance medical science and improve patient outcomes, Centricity Research has a robust history of innovation and collaboration in the clinical research field, making it a pivotal player in the healthcare industry.

How to land this job

  • Position your resume to highlight your clinical coordination skills, emphasizing your experience with study protocols, participant recruitment, and safety procedures as outlined by Centricity Research.

  • Focus on demonstrating your ability to manage study visits, perform clinical assessments such as ECGs and phlebotomy, and maintain accurate documentation and data integrity in compliance with GCP and SOPs.

  • Apply through multiple platforms including Centricity Research's official corporate website and LinkedIn to maximize your application visibility and chances of being noticed.

  • Connect with current Clinical Research Coordinators or research staff at Centricity Research on LinkedIn; use ice breakers like commenting on recent research projects they are involved in or asking about their experience with study participant recruitment to start meaningful conversations.

  • Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical research coordination,' 'GCP,' 'study protocol compliance,' 'participant recruitment,' 'phlebotomy,' and 'data integrity' to ensure it passes automated screenings.

  • Utilize Jennie Johnson's Power Apply feature to automate tailored resume submissions, identify multiple application channels, and find relevant LinkedIn contacts to network with, allowing you to focus more effectively on interview preparation and skill enhancement.

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