Worldwide Clinical Trials
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
Grants Investigator, Specialist
🔥 1 minute ago
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Worldwide Clinical Trials
1001 - 5000 employees
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.
📋 Description
• Develop, deliver, and maintain Investigator Grants exports during the bidding and study template development phases • Work with appropriate teams to ensure accurate, complete, and timely Investigator Grants deliveries • Assist in developing and maintaining processes, policies, SOPs, and related Investigator Grants documents • Advise Commercial Operations, Project Management, Business Development, Site Activation, Clinical Operations, and customers on forecasting strategies and risk mitigation • Review study protocols and coordinate with relevant departments to complete costing strategies for protocol-driven costs • Review study budgets and Investigator Grants operational costs • Participate in Commercial Operations activities • Perform other assigned duties
🎯 Requirements
• Knowledge of global industry-standard benchmarks and fair market value • Proven expertise using investigator grant software such as GrantPlan or Grants Manager globally • Experience reviewing and understanding study protocols, budgets, and technical, medical, and legal documents • Ability to work in a fast-paced, deadline-oriented, changing environment • Strong planning, strategizing, managing, monitoring, scheduling, critiquing, and problem-solving skills • Excellent written and verbal communication, including negotiation skills • Knowledge of clinical trial agreements • Computer expertise with document and spreadsheet applications • Bachelor's degree or equivalent in business administration, law, science, or a related field • Minimum 2 years of experience forecasting Investigator Grants • Knowledge of the biopharmaceutical/CRO industry and applicable local regulatory requirements • Knowledge of global industry benchmarks, fair market value, ICH and GCP Guidelines, and local compensation and regulatory requirements • Excellent spoken and written English language skills • Investigator grant forecasting tools experience preferred
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