Clinical Trial Manager

Description

Venesco LLC is seeking Clinical Trial Managers to provide leadership and operational oversight for FDA-regulated clinical studies, ensuring studies are executed in accordance with approved protocols, budgets, timelines, regulatory requirements, and quality standards.

• Manage all phases of clinical trial startup, conduct, and closeout.
• Develop and maintain project plans and timelines.
• Coordinate protocol development and study documentation.
• Manage Trial Master File (TMF) documentation.
• Coordinate study working groups and stakeholder meetings.
• Ensure Clinical Trials.gov registration and reporting requirements are met.
• Monitor study metrics and status reports.
• Coordinate interactions among sites, CROs, sponsors, and regulatory personnel.
• Identify operational risks and develop mitigation plans.
• Support FDA inspections and sponsor audits.

• Bachelor's degree in Life Sciences or related field.
• Minimum 7 years of clinical trial management experience.
• Experience managing FDA-regulated studies.
• Strong understanding of ICH-GCP and FDA requirements.

Venesco, LLC, is an equal opportunity and affirmative action employer. Venesco is committed to administering all employment and personnel actions on the basis of merit and free of discrimination based on race, ethnicity, religious affiliation, gender, gender identity or expression, sexual orientation, national origin, protected veteran status, or status as an individual with a disability. Consistent with this commitment, we are dedicated to the employment and advancement of qualified minorities, women, individuals with disabilities, protected veterans, persons of all ethnic backgrounds and religions according to their abilities.

For more information on Venesco, LLC., visit