Job summary
Job post source
This job is directly from Eximia Research
Job overview
The Site Start-Up Associate at Eximia Research supports clinical trial initiation by managing regulatory submissions and coordinating start-up activities across the site network.
Responsibilities and impact
The role involves coordinating start-up activities, preparing and submitting regulatory documents, communicating with sponsors and CROs, maintaining compliance trackers, and collaborating with internal teams to ensure site readiness.
Compensation and benefits
The position offers a competitive salary, benefits, and opportunities for advancement within a growing clinical research site network.
Experience and skills
Candidates should have a bachelor's degree in life sciences or related field, 1-3 years experience in site start-up or clinical research, knowledge of ICH-GCP, FDA, IRB requirements, and strong organizational and communication skills.
Career development
The company provides opportunities for professional growth and advancement within its expanding site network.
Work environment and culture
Eximia Research fosters a collaborative and growth-oriented work environment focused on improving patient access to innovative therapies.
Company information
Eximia Research is a growing network of integrated clinical research sites dedicated to advancing healthcare through patient-focused clinical trials across multiple therapeutic areas and locations.
Unique job features
The role is distinguished by its critical involvement in the clinical trial start-up process, working closely with sponsors, CROs, and internal teams to ensure efficient site activation.
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 experience coordinating clinical trial start-up activities, including regulatory submissions and document management, aligning closely with Eximia Research's focus on site activation and compliance.
Highlight familiarity with ICH-GCP guidelines, FDA and IRB requirements, and proficiency in CTMS or similar regulatory tracking systems to demonstrate your readiness for the role's compliance and organizational demands.
Apply through multiple channels such as Eximia Research's corporate careers page and LinkedIn to maximize your application visibility and improve your chances of being noticed by recruiters.
Connect with current employees in the clinical operations or site management divisions at Eximia Research on LinkedIn; use ice breakers like commenting on recent clinical trials they are involved in or expressing enthusiasm about Eximia's mission to advance patient-focused research.
Optimize your resume for ATS by incorporating keywords from the job description such as 'site activation,' 'regulatory submissions,' 'CTMS,' 'ICH-GCP,' and 'document coordination' to ensure it passes automated screening effectively.
Leverage Jennie Johnson's Power Apply feature to automate tailored resume customization, identify multiple application portals, and find relevant LinkedIn contacts so you can focus your energy on meaningful networking and interview preparation.
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