FREE ACCESS
5,000–10,000 jobs/day
See all jobs on Scoutfield
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in Clinical Trial Agreements (CTAs) negotiation, budget development, and financial reconciliation within clinical research. Proficient in managing clinical trial site payments and ensuring compliance with GCP/GXP/ICH regulations.
Highest-signal resume keywords
Clinical Trial Agreement NegotiationBudget Development and Cost AnalysisAccounts Payable ExperienceClinical Site Payments ManagementGCP/GXP/ICH Regulations Knowledge
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial AgreementsBudget DevelopmentCost AnalysisPayment ReconciliationFinancial Systems ManagementData IntegrationContract Milestone TrackingInvoice VerificationPayment Discrepancy ResolutionClinical Trial Operations
Soft Skills
Attention to DetailStrong Analytical SkillsExcellent Communication SkillsOrganizational SkillsCommitment to Quality
Tools & Technologies
Veeva VaultEDC SystemsAdobeExcelMicrosoft WordMicrosoft Outlook
Industry Keywords
Clinical ResearchCRO EnvironmentResearch BillingClinical Trial OperationsRegulatory Compliance
Tech Stack
Tools & technologiesGoogle Cloud PlatformVault
About the role
Key responsibilities & impact- Facilitate the review and execution process for Clinical Trial Agreements (CTAs) and amendments with sponsors, sites, and Ora legal teams
- Support development, review, and negotiation of clinical trial budgets, including per-patient costs, start-up fees, pass-through expenses, and overhead
- Track contract milestones, renewals, and amendments throughout the study lifecycle
- Monitor budget approvals and align contract terms with negotiated budgets
- Ensure payment terms, invoicing schedules, and milestone payments are clearly defined in contracts
- Analyze study protocols for cost implications and ensure budgets reflect fair market value (FMV)
- Prepare reports for study teams regarding contract status, budget approvals, and payment status
- Collaborate with global cross-functional project teams, including Project Management, Clinical Trial Associates, Clinical Research Associates, Project Directors, and IT
- Collaborate with Legal on contract negotiations
- Identify, track, and monitor data integration between EDC and Veeva Vault systems; highlight and follow up on issues causing payment delays
- Set up, process, and manage clinical trial site payments in the Veeva Vault Payment system according to CTAs and approved budgets
- Verify payment triggers are met before payment
- Calculate and reconcile per-patient payments, start-up fees, milestone payments, and pass-through expenses
- Ensure payments are issued accurately and on schedule
- Reconcile payments with invoices, supporting documentation, and financial systems
- Identify and resolve overpayments, underpayments, and payment discrepancies
- Adhere to Ora’s quality system and required compliance, data integrity, business ethics, and regulatory processes
- Demonstrate Ora’s values of kindness, operational excellence, cultivating joy, and scientific rigor
Requirements
What you’ll need- Associate’s or Bachelor’s degree in business or Life Sciences, with one or more years’ experience in clinical research or equivalent combination of education, training and experience
- Years of experience may be considered in lieu of education
- 2+ years of Accounts Payable experience
- High attention to detail and ability to manage multiple studies simultaneously
- Clinical trial contract negotiation and budget development and cost analysis experience
- Experience working at a research site or in a CRO environment
- Knowledge of clinical trial agreements and research billing
- Strong analytical and excellent communication skills
- Experience in clinical site payments and clinical trial operations
- Strong organizational skills with a commitment to consistently producing high quality work
- Experience with Adobe, Excel spreadsheets, Microsoft Word and Outlook
- Knowledge of GCP/GXP/ICH regulations
Benefits
Comp & perks- Comprehensive medical, dental, and vision healthcare options beginning day 1
- Flexible PTO
- Unlimited sick time
- 14 company-paid holidays
- 401(k) plan through Fidelity with company match
- Adoption assistance
- Fertility assistance
- 16 weeks paid parental leave
- Company-paid life insurance
- Company-paid disability insurance
- Remote workspace reimbursement
- Wellness reimbursement
- Employee Assistance Program
- Career development opportunities
- Opportunities to work with colleagues across the globe
- Opportunity to research new ophthalmic therapies with global patient impact
