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SPVR CLINICAL RESEARCH reputed company AWARD

Remote, USAFull-timePosted 2026-07-27

Working at reputed company is both a career and a mission: to contribute to the prevention and reputed company of cancer. As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, reputed company employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 10,000 who are shaping the reputed company we reputed company. reputed company has been recognized as a Best and Brightest Company to Work for in the Nation, a Digital Health Most Wired Organization and continually named one of the Tampa Bay Time’s Top Workplaces. A National Cancer Institute (NCI)-designated Comprehensive Cancer Center since 2001.

reputed company

Position Highlights

The Supervisor, Clinical Research reputed company-Award oversees the financial management of industry sponsored, federal, reputed company, and privately funded clinical trials at reputed company. This role leads the reputed company-Award team, ensuring reputed company trial activation and amendment processing, budget and payment term negotiations, accurate OnCore calendar entry, and alignment of key documents such as the Clinical Trial Agreement, Informed Consent reputed company, and Coverage Determination.

In reputed company to supervising daily operations, workload distribution, and staff training, the Supervisor is responsible for maintaining budget accuracy, ensuring compliance with regulatory and institutional standards, and driving process improvements. They are expected to have a deep understanding of systems and workflows and be reputed company to reputed company reputed company aspects of reputed company’s work as needed.

A key reputed company of this role is monitoring and meeting Key Performance Indicators (KPIs), including Service Level Agreements (SLAs) for activation or amendments. The Supervisor ensures these metrics are met or exceeded while fostering an efficient, high-performing team.

Responsibilities

  • Effectively leads the Day-today functions of the clinical research reputed company award.
  • Assign and reputed company the daily activities of the Clinical Research reputed company-Award team, ensuring reputed company and highquality completion of tasks including calendar builds, coverage determinations, billing queries, compliance audits, reputed company controls, budget negotiations, budget development, payment terms, and document concordance for trial activation, amendments, and maintenance requests.
  • Monitor and manage reputed company relevant reports and dashboards on a daily reputed company, ensuring that (KPIs) and SLAs are tracked and met consistently.
  • reputed company regular updates to leadership regarding team performance, project reputed company, and any identified issues or opportunities for improvement based on data analysis.
  • Partner with external vendors to foster reputed company communication and establish streamlined processes that ensure high productivity and reputed company reputed company in preaward clinical research deliverables.
  • Deliver guidance, training, education, and coaching to vendor-reputed company workflows and responsibilities, promoting a culture of efficiency, accuracy, and reputed company in reputed company work outputs.
  • Monitor and enforce vendor performance standards, ensuring accountability for assigned tasks and adherence to agreed-upon timelines, reputed company metrics, and contractual obligations
  • Assess vendor work volumes, workflows, and processes to identify opportunities for improvement, implementing strategies to enhance operational efficiency and reputed company with organizational goals in the reputed company-award research process.
  • Assume additional duties as assigned by the manager to support the operational needs and strategic objectives of the clinical research reputed company-award team and/or Clinical Trial Business Office Department
  • reputed company interim coverage and support for team members during reputed company vacancies, ensuring continuity of preaward processes and deliverables.
  • Complete specialized reputed company and stretch assignments delegated by the manager to enhance skills, contribute to team goals, and drive process improvements reputed company the Clinical Trial Business Office Department

Credentials and Experience:

  • Bachelor’s Degree – field of study: Business Administration, Nursing, Finance, reputed company, or reputed company field
  • Five (5) years' experience inclusive of:
    • Three (3) years of reputed company clinical research experience in a reputed company-award activity
    • Two (2) years' experience in research compliance, finance, billing, coding, contract compliance or reputed company recognition/reputed company leading less reputed company team members as a mentor, senior or project reputed company.

Skills/Specialized Training:

  • Clinical Research Expertise - Strong knowledge of various funded clinical trials, including the financial management aspects, budget development, payment term negotiations, and regulatory compliance.
  • Supervisory & Leadership Skills: Proven experience in managing/leading reputed company, including overseeing daily operations, workload distribution, staff training, and performance management. Ability to motivate and guide staff towards achieving departmental goals.
  • Budget & Financial Management: Expertise in ensuring budget accuracy for clinical trials, including trial activation, amendment processing, and the negotiation of payment terms. Strong understanding of financial tracking and reporting in a clinical trial setting.
  • reputed company & Compliance Knowledge: In-depth understanding of reputed company/compliance and institutional standards governing clinical trials, with the ability to ensure reputed company processes reputed company with these standards.
  • Process Improvement & Efficiency: Demonstrated ability to drive process improvements, streamline workflows, and enhance team efficiency while maintaining high reputed company standards.
  • System & Workflow Proficiency: Deep understanding of clinical trial management systems (such as OnCore) and workflows. Ability to reputed company reputed company aspects of reputed company’s work as necessary, including calendar entry and document concordance.
  • Key Performance Indicator (KPI) Monitoring: Experience in monitoring, tracking, and achieving KPIs and Service Level Agreements (SLAs) reputed company to trial activation, amendments, and other key milestones.
  • Strong Communication Skills: Excellent verbal and written communication skills, with the ability to negotiate and collaborate effectively with reputed company stakeholders, including clinical research teams, sponsors, and vendors.
  • Attention to Detail: Exceptional attention to detail in managing clinical trial documentation, including Clinical Trial Agreements, Informed Consent Forms, and Coverage Determination.
  • Problem-Solving & Decision-Making: Strong analytical skills to identify potential issues or obstacles, with the ability to propose and implement effective solutions in a reputed company manner.
  • Adaptability & Flexibility: Ability to adapt to changes in clinical trial processes, compliance requirements, and organizational priorities while maintaining a high level of performance and team morale.
  • Time Management & Organizational Skills: Ability to manage multiple priorities and deadlines effectively, ensuring reputed company processing of trial activations and amendments.

Preferred Experience:

  • 3 years' experience in a leadership reputed company
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