The Implementation Specialist will extract data from clinical trial documentation to configure systems for participant payments. They will also collaborate with internal teams and customers to ensure study requirements are met and processes are optimized.
Requirements overview
Candidates must have at least one year of experience in the pharmaceutical or CRO industry with a focus on contract management. Strong proficiency in Microsoft Excel and the ability to interpret complex financial documents are essential for this role.
Key skills
Data extractionSystem configurationContract managementClinical trial documentationExcelMicrosoft WordAnalytical skillsAttention to detailCommunicationTime managementRisk mitigationProcess documentationCustomer relationship managementFinancial document analysis
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Suvoda is a global clinical trial technology company, now strengthened by our merger with Greenphire. Backed by expert teams and rigorous processes, we specialize in complex, life-sustaining studies in therapeutic areas like oncology, central nervous system (CNS), and rare diseases. Together, we support sponsors, sites, and patients to manage the most urgent moments in the most urgent trials through a unified platform featuring RTSM (IRT), eCOA, eConsent, Greenphire Patient Payments, and Greenphire Travel software solutions.
Suvoda is hiring an Implementation Specialist to extract applicable data from customer documentation and translate it into accurate system configurations that support payments to clinical trial participants. Our ideal candidate brings a sharp eye for detail, strong Excel skills, and the ability to learn new systems quickly and work independently as priorities change. They will communicate clearly, collaborate well, and keep a constructive, solutions-oriented approach.
Responsibilities
Review and interpret global customer documentation related to study activities, including but not limited to; contracts, budgets, amendments, ICF's and templates.
Identify areas of quality risk and/or need in pursuit of a best-in-class customer, site, and patient experience.
Apply best practices to extract and configure customer data into applicable study activities from source documents.
Collaborate and communicate with business partners to verify interpretation of study requirements.
Adhere to auditing and monitoring checklists and procedures.
Adhere to both internal KPIs and customer-driven SLAs.
Participate in internal and external calls regarding study implementation and complex configuration issues/needs; consult with customers and Client Delivery colleagues to achieve resolution and adhere to best practices.
Contribute to internal process documents to ensure study configurations are consistent and follow best practices.
Partner with Product and IT teams to identify areas of enhancement across platforms.
Support Client Delivery in establishing and maintaining positive customer relationships.
Perform other duties, assignments, and/or special projects as time or circumstances necessitate.
Qualifications
At least 1 year of previous experience in the pharmaceutical or CRO industry with contract management-related experience preferred
Experience with Microsoft Word and Excel required
Strong attention to detail required
Ability to dissect the key elements of clinical trial financial documents and identify payable activities
Ability to handle high volume in a fast-paced environment
Excellent writing skills
A mindset of quality and risk mitigation in pursuit of the best client, site, and patient experience required
Must have excellent analytical, organizational, communication, and interpersonal skills
Exceptional time management skills to support shifting priorities and key client deliverables
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As set forth in Suvoda’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.
If you are based in California, we encourage you to read this important information for California residents linked here.
Requirements
•Data extraction
•System configuration
•Contract management
•Clinical trial documentation
•Excel
•Microsoft Word
•Analytical skills
•Attention to detail
•Communication
•Time management
•Risk mitigation
•Process documentation
•Customer relationship management
•Financial document analysis
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