At a Glance
- Tasks: Ensure compliance and manage regulatory documents for clinical trials across multiple sites.
- Company: Alcanza Clinical Research, a leader in clinical trial management.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Join a dynamic team dedicated to making a difference in healthcare.
- Why this job: Play a crucial role in advancing medical research and improving patient outcomes.
- Qualifications: Attention to detail and experience in regulatory processes are essential.
The predicted salary is between 72000 - 88000 $ per year.
Alcanza Clinical Research is seeking a Regulatory Specialist to ensure GCP/SOP compliance across multiple sites.
You will manage regulatory documents, liaise with IRB and sponsors, and lead quality control and staff training on regulatory processes.
Responsibilities include maintaining study files, coordinating regulatory filings, distributing safety reports, and supporting audits to keep essential documents up-to-date and audit-ready.
A strong attention to detail is essential.
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Clinical Trials Regulatory Specialist in Burlington employer: ActivMed Practices & Research, LLC.
Alcanza Clinical Research is an exceptional employer that fosters a collaborative and inclusive work environment, making it an ideal place for a Compensation Analyst to thrive. With a strong commitment to employee growth, we offer comprehensive benefits, including medical, dental, and retirement plans, while promoting a culture of respect and dignity. Join us in our mission to make a meaningful impact in clinical research across multiple therapeutic areas, where your contributions will directly enhance the quality of life for countless patients.
Contact Details:
ActivMed Practices & Research, LLC. Recruitment Team
