Experts Corner

With a strong academic foundation and years of hands-on experience in the industry, throughout her career, Erika held various roles in research compliance; progressively expanding her responsibilities and honing her expertise.

Our VP experience encompasses:

• Developing and implementing compliance programs and policies tailored to the unique needs of clinical research organizations.
  
• Conducting comprehensive compliance audits and assessments to identify areas for improvement and ensure adherence to regulatory requirements.
  
• Providing expert guidance and training to research teams on compliance obligations, ethical considerations, and best practices in clinical research.
  
• Collaborating with cross-functional teams, including legal, regulatory affairs, and quality assurance, to address compliance-related issues and drive continuous improvement initiatives.

Erika is deeply committed to upholding the highest standards of integrity, ethics, and compliance in clinical research. She approaches her role with a proactive and solution-oriented mindset, viewing compliance as an essential component of ensuring the safety, integrity, and ethical conduct of research activities.