
Clinical Research Systems Study Build Specialist
Posted 5 days ago

Posted 5 days ago
This is a fully remote position, open to applicants in Florida.
• Develop and sustain financial study builds within CTMS systems in accordance with study protocols, contract stipulations, and Alcanza guidelines.
• Oversee ticketing-system requests for new builds and modifications.
• Collaborate with Operations and Finance teams to prioritize study builds and ensure timely completion.
• Verify that billing determinations, sponsor budgets, and clinical trial agreements are consistent with protocols and site needs.
• Execute quality control measures to uphold study-build integrity and enhance future cash flow.
• Detect protocol requirements that are absent from clinical trial agreements and assist in ensuring that contractual commitments are fulfilled.
• Work together with Operations, Budgets/Contracts, Systems, and Finance teams to establish scalable best practices.
• Engage in process standardization, system migrations, CTMS/eSource integrations, and the assimilation of processes and systems from acquired sites.
• Recognize opportunities for business-process enhancements and efficiency improvements.
• Carry out other assigned responsibilities.
• An associate degree is required; a bachelor's degree in accounting, finance, business, sciences, or a related field is preferred.
• A minimum of 2 years of experience in the clinical research industry or an equivalent combination of education and experience is necessary.
• Proficient in entering calendar details, study budget elements, and financials into a CTMS system is required.
• Experience with Clinical Conductor is necessary.
• Competency in Microsoft applications, email, electronic health records, and web applications is required.
• Ability to type proficiently at a rate of 40+ words per minute.
• Strong organizational abilities, time management skills, attention to detail, and mathematical proficiency are essential.
• Well-developed written and verbal communication skills are required.
• Strong interpersonal and listening skills; capability to work independently as well as collaboratively with co-workers, subjects, managers, and external customers.
• Ability to manage multiple responsibilities and adapt to shifting workloads and priorities.
• Demonstrates professionalism, respect for others, self-motivation, and a robust work ethic.
• High levels of integrity and dependability are essential.
• Capable of working with minimal supervision, identifying issues, and implementing solutions.
• Proficient in handling highly sensitive information with confidentiality and professionalism, in accordance with privacy and company policies.
• Full-time employees scheduled to work at least 30 hours per week are eligible for benefits, with coverage beginning on the first day of the month following the hire date.
• Benefits include medical, dental, vision, life insurance, short and long-term disability insurance, health savings accounts, supplemental insurances, and a 401k plan with a safe harbor match.
Thermo Fisher Scientific
ICON plc
ICON plc
Clinical Outcomes Solutions
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