Clinical Research Operations Manager

Amazing Opportunity for an experienced Site Manager to join a very well established company in the San Antonio area of Texas.

Highlights

• Play a major role in cutting-edge clinical trials - a meaningful healthcare position!
• Full Benefits (Health, Dental, Vision, 401k w/ 4% Match, PTO, Paid Holidays)
• Gain experience in the fast-growing world of clinical research and develop skills that are in high-demand

Company:

Our client is a Clinical Research site network with over 24 research sites across the seven states. Their sites conduct Phase I-IV trials in therapeutic areas like cardiology, metabolic disorders, renal, CNS, pulmonology, and vaccines.

Position:

A Clinical Research Site Manager oversees the daily operations of clinical research sites, ensuring studies are conducted in compliance with regulatory standards and protocols. They manage site staff, recruitment, data collection, and ensure patient safety throughout the study.

Key Responsibilities:

• Study Management: Oversee protocol implementation, patient enrollment, and data collection.
• Team Leadership: Supervise site staff and ensure effective team communication.
• Regulatory Compliance: Ensure adherence to regulatory requirements, prepare necessary documents, and handle audits.
• Quality Assurance: Monitor study accuracy, resolve issues, and implement corrective actions.
• Budget & Resources: Manage site budgets and ensure efficient use of resources.
• Communication & Reporting: Serve as the main contact with sponsors and external partners, providing regular study updates.

Skills & Qualifications:

• Skills: Strong project management, problem-solving, attention to detail, and communication skills.
• Education: Typically requires a bachelor’s degree in life sciences or a related field.
• Experience: 3 years in clinical research or trial coordination.
• Management: 1 year management within a Clinical Research setting.
• Certifications: CRC, CRA certifications are a plus.