Site Contracts and Budget Manager

Role Summary:

• Primary focus is global clinical trial budget template development from study documentation.
• Secondary responsibility for reviewing and negotiating site contracts and legal agreements.

Key Responsibilities:

• Translate complex protocols into detailed budget templates with site-level costs.
• Develop per-patient, per-visit, and conditional costs for budget templates.
• Review and negotiate confidentiality agreements, master services agreements, and clinical study agreements.

Qualifications:

• Graduate degree or 4-year college degree required.
• Minimum 5 years of relevant clinical research experience with budget template development.
• Experience in a CRO, pharmaceutical, or healthcare environment.

Skills:

• Strong organizational and communication skills with attention to detail.
• Proficient in MS Office software and computer applications.
• Ability to interpret complex protocols and study documentation.