Sr. Clinical Research Budget Analyst

Responsibilities

• Responsible for the development of study budgets and negotiations to external funding agencies and sponsors including industry and contract research organizations.
• Works closely with PI and study team to ensure that all expenses are captured accurately in the budget.
• Facilitates ancillary department budgeting including lab, radiology, PCI, investigational pharmacy as needed for each study.
• Strives to meet expected turn around times for budget development and negotiation.
• Provides training and support for complex budget topics to junior team members, and the research community as needed.
• Participates in research coordinator training as needed by developing and delivering presentations at monthly meetings or quarterly orientations as needed.
• Supports the CTO manager in the development of routine productivity reports as needed.
• Participates in QA/QI initiatives as assigned.
• Completes financial build in OnCore Clinical Research Management Systems (CRMS).
• Acts as a resource in patient care billing compliance, participating in training and education as needed.
• Acts as a resource in the development of internal policies, procedures and job aides related to clinical trial billing.

Requirements

• Use of computers and web-based applications in a security-focused environment.
• Critical thinking skills – ability to analyze clinical research protocols, assess study budgets, and analyze clinical trial contracts including payment terms.
• Excellent communication skills, ability to interact across the organization, and negotiate with clinical research sponsor/clinical research organization personnel in a professional manner to represent CNH.
• Ability to work well with faculty, staff and across multiple teams to accomplish common goals.

Skills/Knowledge

• Use of computers and web-based applications in a security-focused environment.
• Critical thinking skills – ability to analyze clinical research protocols, assess study budgets, and analyze clinical trial contracts including payment terms.
• Excellent communication skills, ability to interact across the organization, and negotiate with clinical research sponsor/clinical research organization personnel in a professional manner to represent CNH.
• Ability to work well with faculty, staff and across multiple teams to accomplish common goals.

Qualifications

• Minimum Education: Bachelor's Degree Sciences, Health Administration, Computer Science or equivalent with the minimum required experience.
• Minimum Work Experience: 5 years Prior clinical trials experience either as clinical research coordinator or in clinical research administration in academic institutions, biopharmaceuticals or CRO.

Benefits

Not specified.

Pay

Not specified.

Schedule

Not specified.

About the Role

Completes budget development, sponsor negotiations and revenue cycle operational activities for clinical trials activities. Reports to the Manager of Clinical Trials Office. Clinical research experience and familiarity with database systems is recommended, including working knowledge of IRB, ICH/GCP guidelines, federal and state guidelines, and regulations and laws that govern research administration.