Job Description

The Scientific team with Russell Tobin is seeking a Medically Certified Clinical Research Coordinator.

Job Description:

This Clinical Coordinator will plan and execute clinical studies, including but not limited to, protocol & document creation, recruitment, consenting, screening, and conducting study visits.
A successful coordinator will be knowledgeable in each of the provided areas but also demonstrate a flexible and enthusiastic mindset in establishing new and creative approaches.
This role will require creative and critical thinking, attention to detail, and a strong ability to prioritize efforts.

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Employment Type: Contract/ Onsite

Location: Mesa, AZ area

Pay rate : $50-57/hr, based on experience

Responsibilities:

• Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Dexcom’s SOPs
• Execute assigned clinical trials including start up, subject recruitment & scheduling, consenting, screening, subject training, collection of regulatory documents, conducting study visits, performing SMBG testing, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, and providing IRB close-out reports
• Responsible for identifying and escalating safety events and major protocol deviations
• Collaborate with project management to establish and maintain study timelines.
• Manage all clinical tasks and deliverables to meet clinical timeline
  Assist with the management of studies by coordinating daily operations including methods, workflow and implementation of procedures.
• Assist with developing clinical study materials (including, but not limited to, source documentation, CRFs, IRB submissions, training slides, etc.) under supervision.
• Coordinate preparation of key documents for trial site submission to IRBs.
• Assists management with departmental audits of clinical studies and procedures.
• Collaborate effectively with peers and leadership across departments and can professionally interact/build relationships with FDA, IRB, and key opinion leaders.

Requirements:

• Bachelor’s degree in a technical discipline, and a minimum of 2-5 years related experience
• Must have an active Medical Certificate in the State of Arizona
  • RN, LPN, LVN, CNA, EMT
• Proficient with MS Office Suite (Excel, Word and PowerPoint) and MS Project
• Knowledge of GCP (Good Clinical Practice)

Nice to have Skills:

• Certification as a clinical research associate or coordinator (e.g., CCRA, CCRC)
• Monitoring clinical studies experience or experience as a study coordinator is a plus
• Clinical Trial Management System (CTMS) experience.
• Experience in continuous glucose monitoring (CGM) is a plus.

Benefits that Russell Tobin offers:

Russell Tobin offers eligible employee’s comprehensive healthcare coverage (medical, dental, and vision plans), supplemental coverage (accident insurance, critical illness insurance and hospital indemnity), a 401(k)-retirement savings, life & disability insurance, an employee assistance program, identity theft protection, legal support, auto and home insurance, pet insurance, and employee discounts with some preferred vendors. 

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Rate/Salary: $50-57/hr

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