Job summary
Job post source
This job is directly from Eximia Research
Job overview
The Clinical Research Coordinator at Eximia Research manages clinical trials from start to finish, ensuring compliance with protocols and regulatory standards to support the company's research goals.
Responsibilities and impact
The CRC will conduct and manage clinical trials, coordinate study activities including recruitment, data entry, regulatory submissions, and adverse event reporting, while ensuring quality control and effective communication among stakeholders.
Experience and skills
Requires a Bachelor's degree and 2 years of CRC experience, certifications in phlebotomy and dose administration if applicable, and certification as a Clinical Research Coordinator within six months; advanced medical terminology knowledge and strong organizational, communication, and problem-solving skills are essential.
Company information
Eximia Research is a network of premier investigational sites known for excellent trial execution, rapid recruitment, and quality data delivery, serving global biopharmaceutical and clinical research organizations.
Company overview
Eximia Research is a nationwide leader in clinical research, specializing in multi-therapeutic clinical trials. Based in Dover, Delaware, and with significant operations in St. Louis, Missouri, the company operates a network of high-quality research sites. Eximia serves the clinical research needs of global biopharmaceutical companies, providing essential research across a diverse range of therapeutic areas. Recently, VSS Capital Partners made a growth capital investment in Eximia, underscoring its robust operational track record and potential for further expansion.
How to land this job
Tailor your resume to emphasize your experience managing clinical trials according to GCP, ICH guidelines, and SOPs, highlighting your ability to coordinate all phases from startup to closeout.
Showcase your proficiency in project management, risk mitigation, and quality control strategies within clinical research settings, emphasizing your skills in vendor management, subject recruitment, and regulatory compliance.
Apply to the Clinical Research Coordinator position through multiple channels including Eximia Research’s corporate careers site and LinkedIn to maximize your application visibility.
Connect with current employees in the clinical research or trial management teams at Eximia Research on LinkedIn; use ice breakers such as commenting on recent trials they’ve managed or asking about their experience with Eximia’s rapid recruitment strategies.
Optimize your resume for ATS by incorporating key terms from the job description such as 'clinical trial management,' 'GCP,' 'ICH guidelines,' 'regulatory documents,' 'subject recruitment,' and 'data quality control' to ensure your resume passes initial screenings.
Utilize Jennie Johnson’s Power Apply feature to automate tailoring your resume, identify the best application platforms, and discover LinkedIn contacts for networking, allowing you to focus your energy on preparing for interviews and further skill development.
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