Job summary
Job post source
This job is directly from Celerion
Job overview
The Clinical Project Coordinator at Celerion supports clinical study management to ensure timely, compliant, and quality execution of clinical trials, contributing to faster drug development.
Responsibilities and impact
The role involves assisting project and site management, supporting study implementation, document management, monitoring visit preparations, regulatory compliance, and communication with sponsors and clients to ensure study progress and quality.
Experience and skills
Requires a bachelor's degree in biomedical or life sciences, strong communication, organizational, and time management skills, knowledge of Good Clinical Practice and regulatory requirements, and the ability to work independently and in teams.
Work environment and culture
Celerion values integrity, trust, teamwork, and respect, promoting continuous training and knowledge sharing in a remote work environment.
Company information
Celerion is a clinical research company focused on translational medicine to accelerate drug development and market entry.
Job location and travel
This is a remote, work-from-home position available anywhere in the US.
Unique job features
The job offers the opportunity to work remotely while supporting global clinical development projects with a focus on quality and regulatory compliance.
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 project coordination, emphasizing skills in project management, regulatory compliance, and document management as outlined by Celerion's Clinical Project Coordinator role.
Focus on demonstrating your knowledge of Good Clinical Practice, 21 CFR Part 11, and your ability to support study milestones, site management, and Sponsor/Client interactions to align with the job’s primary responsibilities.
Apply through multiple channels including Celerion’s corporate career site and LinkedIn to maximize your application visibility and ensure your resume reaches the right recruiters.
Connect with professionals working in Celerion’s Global Clinical Development team on LinkedIn; start conversations by mentioning your enthusiasm for clinical research, or inquire about recent projects or the team’s approach to clinical trial management as ice breakers.
Optimize your resume for ATS by incorporating keywords from the job description such as 'clinical project management,' 'regulatory compliance,' 'Good Clinical Practice,' 'document management,' and 'study milestone tracking' to improve your chances of passing initial screenings.
Use Jennie Johnson's Power Apply feature to automate tailored resume submissions across multiple platforms and identify relevant LinkedIn contacts, allowing you to focus your time on preparing for interviews and networking effectively.
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