Lead Clinical Research Associate - Contract

About the Job:

• Lead and direct the CRA and CTA team for assigned studies.
• Ensure timely and accurate initiation, enrollment, conduct, and completion of studies.
• Identify quality issues and establish action plans with the study team.

Responsibilities:

• Act as primary liaison between CRAs, internal staff, site staff, and external vendors.
• Oversee clinical monitoring activities per SOPs, regulations, and study requirements.
• Manage clinical plans, guidelines, timelines, and data discrepancies.

Qualifications:

• RN, Bachelor's degree in biological sciences or related field, or equivalent experience.
• Previous CRA experience preferred.
• Extensive knowledge of FDA regulations and practical implementation.

Additional Information:

• Willingness to travel and perform remote and on-site monitoring if needed.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Equal opportunity employer committed to a workplace free from discrimination.