Clinical Trial Reasearch & Budget Specialist

Swoon; United States; Vor Ort; USD 65.000 - 95.000; Vollzeit

Zusammenfassung

Swoon seeks a Clinical Research Administrative Specialist to support the Research Office team in a managed services environment. The role centers on building and reviewing clinical trial budgets, coverage analysis, and study calendars to enable budget development and negotiation.

You will work with CTMS and sponsor stakeholders, manage multiple studies for diverse clients, and contribute to process improvements.

Qualifikationen

• Bachelor's degree in a related field preferred, but equivalent hands-on experience may be considered.
• 3+ years of clinical research administration experience
• Experience with coverage analysis
• General data analysis and financial tracking
• Strong written and verbal communication skills
• Ability to work independently and manage multiple projects/client needs

Aufgaben

• Develop clinical trial budgets, including building budgets from scratch
• Review and QA clinical trial budgets for accuracy and completeness
• Negotiate budgets with sponsors and other external stakeholders
• Support financial feasibility and study financial analysis
• Assist with coverage analysis and research billing determinations
• Review clinical trial protocols and related documentation
• Develop and maintain study calendars and other trial documentation
• Work within clinical trial management systems (CTMS)
• Support industry, federally sponsored, and investigator-initiated studies
• Manage multiple client projects/studies in a consulting environment
• Communicate with internal teams and external client stakeholders
• Contribute to process improvements and provide guidance to more junior team members as appropriate

Kenntnisse

Budget development

Budget negotiation

CTMS experience

Data analysis

Communication

Ausbildung

Bachelor's degree preferred

Tools

CTMS

Sponsor invoicing

Jobbeschreibung

Our client is looking for Clinical Research Administrative Specialists to support their Research Office team within a managed services environment. The team provides back-office support for clinical research studies, including clinical trial budgets, coverage analysis, study calendars, and other trial documentation.

The immediate need is heavily focused on clinical trial budget development and negotiation.

Candidates should have hands-on experience building, reviewing, and negotiating clinical trial budgets—not simply exposure to budgets or working around the budgeting process.

What You'll Be Doing

• Develop clinical trial budgets, including building budgets from scratch
• Review and QA clinical trial budgets for accuracy and completeness
• Negotiate budgets with sponsors and other external stakeholders
• Support financial feasibility and study financial analysis
• Assist with coverage analysis and research billing determinations
• Review clinical trial protocols and related documentation
• Develop and maintain study calendars and other trial documentation
• Work within clinical trial management systems (CTMS)
• Support industry, federally sponsored, and investigator-initiated studies
• Manage multiple client projects/studies in a consulting environment
• Communicate with internal teams and external client stakeholders
• Contribute to process improvements and provide guidance to more junior team members as appropriate

Required:

• Bachelor's degree in a related field preferred, but equivalent hands-on experience may be considered.
• 3+ years of clinical research administration experience
• Experience with coverage analysis
• General data analysis and financial tracking
• Strong written and verbal communication skills
• Ability to work independently and manage multiple projects/client needs

Strongly Preferred

• Experience building budgets from scratch
• Experience with financial feasibility and study financials
• Experience with sponsor invoicing
• Knowledge of clinical trial policy and research billing rules
• Coverage analysis experience
• Experience with clinical trial management systems (CTMS)
• Experience within a Sponsored Research Office, Central Research Office, academic medical center, teaching health system, or cancer institute
• Experience supporting multiple studies, clients, or projects
• Oncology or other complex clinical trial experience