Careplix is seeking a Clinical & Compliance Associate I to oversee regulatory specialists at clinical research sites. The role involves ensuring timely regulatory submissions, maintaining IRB documentation, and ensuring compliance with evolving clinical research regulations.
Key Responsibilities:
✔ Oversee multiple regulatory specialists at clinical research sites.
✔ Ensure timely regulatory submissions and compliance with guidelines.
✔ Maintain and manage IRB (Institutional Review Board) documentation.
✔ Provide training oversight and coordinate audits.
✔ Maintain accurate study records and ensure regulatory compliance.
✔ Demonstrate strong communication, leadership, and multitasking skills.
Eligibility Criteria:
- Education: Bachelor’s degree in Clinical Research or related field.
- Experience:Â 2-5 years in clinical research regulatory affairs.
- Skills:Â Strong knowledge of regulatory compliance, attention to detail, and leadership abilities.
About Careplix
Careplix is a reputed name in the clinical research and contract research industry, known for its commitment to regulatory compliance and high-quality research standards. With a 3.23 rating based on employee reviews, Careplix offers a dynamic work environment for professionals looking to grow in the clinical research domain.
How to Apply
