Investigator – Grants Specialist

🔥 5 minutes ago

🌐 Canada, Mexico, +1 more countries – Remote

🇨🇦 Canada – Remote 🇲🇽 Mexico – Remote 🇧🇷 Brazil – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

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 and disseminate Investigator Grants for pre- and post-award activities • Support various groups related to Investigator Grants delivery • Report directly to the Investigator Grants Manager • 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 associated 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 liaise with relevant departments to complete costing strategies for protocol-driven costs • Review study budgets and costs related to Investigator Grants operations • Participate in Commercial Operations activities • Perform other duties as assigned

🎯 Requirements

• Knowledge regarding global industry standard benchmarks and fair market value • Proven expertise using investigator grant software, such as GrantPlan or Grants Manager, on a global level • Experience reviewing and understanding study protocols, study budgets, and technical, medical, and legal documents related to Investigator Grants • Ability to work in a fast-paced, deadline-oriented, and changing environment • Strong planning, strategizing, managing, monitoring, scheduling, critiquing, and problem-solving skills • Excellent written and verbal communication and 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 of 2 years of experience in forecasting Investigator Grants • Adept knowledge of the biopharmaceutical/CRO industry and applicable local regulatory requirements • Knowledge and understanding of global industry standard benchmarks, fair market value, ICH and GCP Guidelines, and local compensation and regulatory requirements • Excellent spoken and written English language skills • Experience with investigator grant forecasting tools, such as GrantPlan or Grants Manager, preferred

🏖️ Benefits

• Equal employment opportunities regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law