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Worldwide Clinical TrialsSource d’offres vérifiée

Specialist, Investigator Grants

Offre en anglaisExpiré
  • Canada
  • Télétravail
  • Publié 7 sept. 2026
  • 1 poste
Type d’emploi
Temps plein
Niveau d’expérience
Intermédiaire · 2+ ans
Formation minimale
Baccalauréat
Postuler avant le
7 oct. 2026
Langue de l’offre
anglais
Heures de travail
40 heures par semaine
Exigences de lieu
Country, Québec, Quebec, Canada
Niveau d’expérience
Entry level

Ce poste est expiré

Ce poste chez Worldwide Clinical Trials n’accepte plus de candidatures. L’offre originale reste disponible ci-dessous à titre de référence.

Expiré le 18 sept. 2026

Offre d’emploi originale

The Specialist is responsible for the development, dissemination, and maintenance of Investigator Grants during the bidding and template development phases. They collaborate with cross-functional teams to ensure accurate costing strategies and risk mitigation for protocol-driven costs.

Détails du poste

Who We Are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! What You Will Do The Investigator Grants Specialist is responsible for the development and dissemination of Investigator Grants (pre and post-award) while supporting various groups related to Investigator Grants delivery. Reports directly to the Investigator Grants Manager. Responsible for the development, delivery and maintenance of Investigator Grants exports during the bidding phase and during the template development phase of a study Works closely with appropriate teams to ensure accurate, complete and timely deliveries of Investigator Grants. Assists in the development and maintenance of processes, policies, SOPs and associated documents concerning Investigator Grants. Liaises with the Investigator Grants team and advises Commercial Operations, Project Management, Business Development, Site Activation, Clinical Operations and Customers on forecasting strategies/risk mitigation surrounding Investigator Grants. Review study protocols and liaise with competent departments as needed to complete a costing strategy for protocol-driven costs. Review study budgets and costs pertaining to Investigator Grants operations and participate in Commercial Operations activities. Perform other duties as assigned. The duties and responsibilities listed above are representative of the nature and level of work assigned and are not necessarily all-inclusive. What You Will Bring To The Role Knowledge regarding global industry standard benchmarks, fair market value, and proven expertise using investigator grant software (i.e., GrantPlan, Grants Manager) on a global level. Experience in reviewing and understanding study protocols, study budgets, as well as other technical, medical and legal documents related to Investigator Grants. Ability to work in fast-paced, deadline oriented, and changing environment Strong planning, strategizing, managing, monitoring, scheduling, critiquing and problem solving skills Excellent written and verbal communication skills, including negotiation skills and knowledge of clinical trial agreements to clearly and concisely present information. Computer expertise with document and spreadsheet applications. Your Experience Bachelor's degree or equivalent in business administration, law, science or related field. Minimum of 2 years of experience in forecasting Investigator Grants. Adept knowledge of biopharmaceutical/CRO industry and applicable local regulatory requirements. Knowledge and understanding of global industry standard benchmarks, fair market value, ICH and GCP Guidelines, as well as local compensation and regulatory requirements. Excellent spoken and written English language skills. Prefer experience with investigator grant forecasting tools (i.e. GrantPlan, Grants Manager) Promotion to the next level is not automatic based on years of experience. Personnel are evaluated on proven competency, level of responsibility, and ability to work independently. We love knowing that someone is going to have a better life because of the work we do. To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn. Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants 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.

Ce que vous ferez

The Specialist is responsible for the development, dissemination, and maintenance of Investigator Grants during the bidding and template development phases. They collaborate with cross-functional teams to ensure accurate costing strategies and risk mitigation for protocol-driven costs.

Exigences

Candidates must have a bachelor's degree in business, law, science, or a related field and at least 2 years of experience in Investigator Grants forecasting. Proficiency in grant software and knowledge of global industry benchmarks and GCP/ICH guidelines are required.

Compétences indiquées

  • written communication · Souhaitée
  • Résolution de problèmes · Souhaitée
  • Budgeting · Souhaitée
  • Regulatory Compliance · Souhaitée
  • Negotiation · Souhaitée
  • Gestion de projet · Souhaitée

Autres compétences pertinentes

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

  • Investigator Grants Forecasting
  • Fair Market Value Analysis
  • GrantPlan
  • Grants Manager
  • Study Protocol Review
  • Budgeting
  • Clinical Trial Agreements
  • Negotiation
  • Project Management
  • Regulatory Compliance
  • ICH Guidelines
  • GCP Guidelines
  • Spreadsheet Applications
  • Written Communication
  • Verbal Communication
  • Problem Solving

Domaines d’emploi

  • Science & Research
  • Healthcare
  • Finance & Accounting
  • Management & Leadership
  • Consulting

Postes actuels chez Worldwide Clinical Trials

Ces possibilités vérifiées acceptent toujours des candidatures.