Job summary
Job post source
This job is directly from Celerion
Job overview
The Clinical Conduct Specialist at Celerion supports clinical study managers and conduct staff to ensure smooth study preparation and execution, impacting the efficiency of clinical research.
Responsibilities and impact
The role involves assisting study managers with study setup, training conduct staff, ordering supplies, preparing clinic flow, leading the conduct team, participating in client meetings, and ensuring proper study conduct and equipment maintenance.
Compensation and benefits
The position offers an hourly wage of $21 and includes benefits with a full-time schedule requiring flexibility including early mornings and weekends.
Experience and skills
Preferred qualifications include post high school education in life sciences or medical training, at least 6 months internal experience, organizational skills, effective communication, and experience in a medical environment.
Work environment and culture
Celerion values integrity, trust, teamwork, and respect, fostering a supportive and inclusive work environment.
Company information
Celerion is a clinical research company focused on accelerating drug development through translational medicine and innovative research strategies.
Team overview
The candidate will work closely with Clinical Conduct Associates, Technicians, and Phlebotomists across shifts, providing leadership and coordination.
Job location and travel
The position is based in the Tempe clinic with a Monday to Friday schedule from 6:30 AM to 2:30 PM, requiring flexibility for early mornings and weekends.
Unique job features
The role includes unique responsibilities such as process audits, clinical equipment maintenance, and enhancing the study participant experience, distinguishing it from similar positions.
Company overview
Celerion is a leading contract research organization (CRO) specializing in early clinical research and clinical pharmacology. They provide comprehensive services including clinical trials, bioanalytical services, and data management to pharmaceutical and biotechnology companies. Founded in 2010, Celerion has a strong history of accelerating drug development through innovative approaches and state-of-the-art facilities. Their revenue is primarily generated through partnerships with clients seeking to bring new medications to market efficiently and safely.
How to land this job
Position your resume to highlight your experience in clinical study support, focusing on your ability to assist Clinical Study Managers with study preparation and set up, as this is a core responsibility at Celerion.
Emphasize your organizational skills, multitasking abilities, and experience in medical or clinical environments, especially any training you have done related to dosing, blood processing, or sample shipping, since these are key tasks.
Apply through multiple platforms including Celerion's corporate careers page and LinkedIn to maximize your chances and ensure your application is seen by different hiring teams.
Connect with current Clinical Conduct Specialists or Study Managers at Celerion on LinkedIn to learn more about the role and company culture; potential ice breakers include asking about their experience with study-specific training or how they handle multi-shift coordination.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical study preparation,' 'study conduct,' 'training,' 'medical supplies ordering,' and 'process audits' to ensure your resume passes initial automated screenings.
Use Jennie Johnson's Power Apply feature to automate applying through multiple channels, tailor your resume with relevant keywords, and identify LinkedIn contacts to network with, freeing you to focus on interview preparation and other job search activities.
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