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Publié il y a 4 mois

Budget Specialist, Clinical Research

@ Probity Medical Research Inc

Waterloo, Ontario

Temps plein1+ ans d’expérience
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Probity Medical Research is hiring a Budget Specialist in Waterloo, Ontario, for a full-time role. The work involves developing, reviewing and negotiating clinical trial budgets with sponsors, CROs and research sites. The posting states hybrid or remote eligibility and Monday to Friday, 9:00 AM to 5:00 PM hours.

Responsabilités :

  • Review, negotiate and finalize study budgets and amendments
  • Communicate with sponsors, CROs and sites on budgets
  • Update and monitor KPI tracker for sites and projects
  • Coordinate with Contracts team on budget alignment
  • Support process improvements and onboarding of new team members

Résumé des exigences :

  • Bachelor's degree or college diploma in clinical research or life sciences
  • 1+ year as clinical research coordinator or assistant, or 2+ years in clinical research administration
  • Experience negotiating study budgets is an asset
  • Excel proficiency
  • DocuSign and PDF software experience

Outils et compétences

Source et dates

Site carrière / système de candidatures · adp

Date publiée par l’employeur
2026-07-28
Première détection par notre source
2026-10-08
Mise à jour du dossier source
2026-11-09

Ces dates décrivent le dossier source, pas une vérification en direct du recrutement. Consultez l’offre originale.

Détails du poste

NiveauDébutant
DomaineOpérations
Expérience1 an(s) et plus
Heures par semaine40
Horairejour
Milieu de travailBureau
PositionSurtout assis
Exigences physiquesphysique faible · ordinateur élevé
LanguesEnglish
FormationCollégial (DEC) (exigé), Baccalauréat (exigé)
Domaines d’étudesClinical Research, Health Sciences, Life Sciences

Résumé et détails rédigés par l’IA à partir de l’offre; l’offre de l’employeur fait foi.

Probity Medical Research Inc

Profil d’entreprise sauvegardé

Renseignements historiques provenant d’un profil The Jobs API sauvegardé (champs LinkedIn/Crunchbase). Ils ne sont pas vérifiés en temps réel; les chiffres peuvent avoir changé. Les valeurs manquantes restent inconnues.

Aesthetics | Allergy/Immunology | Cardiology | Derm | Endocrine | Rheum | Weight Management | Clinical Research Sites

Description complète de l’entreprise

Probity Medical Research (PMR) is a leading clinical research consortium with over 75 clinical trials sites. PMR's network conducts clinical trials in Aesthetics, Allergy / Immunology, Cardiology, Dermatology, Endocrinology, Rheumatology and Weight Management. The affiliated sites span the US, Canada, Australia and Chile. Across 30 years of research experience, PMR has conducted over 1,400 research studies, working on over 160 conditions and enrolling more than 38,800 participants.

Abonnés LinkedIn
2 365
Personnes associées sur LinkedIn
101
Bureaux déclarés
  • 139 Union St E, Waterloo, Ontario N2J 1C4, CA
Catégories d’activité
  • Training
  • Consulting
  • Medical
  • Financial Services
Autres noms enregistrés
  • Probity Medical Research Inc
  • Probity Medical Research Inc. (PMR)
Spécialités
  • Dermatology
  • Rheumatology
  • Allergy
  • Cardiology
  • Aesthetics
  • Immunology
  • Vaccines
  • Clinical Study
  • and Research Trial
Le profil indique une agence de recrutement
Non
Investissement total déclaré
0

La devise et la date d’observation ne sont pas fournies; ce n’est ni une valorisation actuelle ni une ronde de financement.

Probity Medical Research (PMR) is a leading clinical research consortium with over 75 clinical trials sites. PMR's network conducts clinical trials in Aesthetics, Allergy / Immunology, Cardiology, Dermatology, Endocrinology, Rheumatology and Weight Management. The affiliated sites span the US, Canada, Australia and Chile. Across 30 years of research experience, PMR has conducted over 1,400 research studies, working…

ChampValeur
SecteurResearch Services
Taille51-200 employees
Siège socialWaterloo, Ontario
Type d’organisationPrivately Held
Fondée en1995
SpécialitésDermatologyRheumatologyAllergyCardiology AestheticsImmunologyVaccinesClinical Studyand Research Trial
Offres sur Jobsy6
LinkedInVoir la page
Description

Based in Waterloo, Ontario, Probity Medical Research (PMR) is a Canadian organization supporting the advancement of clinical research by partnering with research sites, pharmaceutical companies, and contract research organizations. Through our specialized administrative services, we help clinical research teams deliver studies that contribute to the development of new treatments and therapies.

At PMR, employees have the opportunity to contribute to meaningful work while developing specialized knowledge within the clinical research industry. Our teams collaborate across departments and with external partners, providing employees with exposure to a variety of projects, stakeholders, and opportunities to expand their skills.

As a growing organization, we value individuals who are eager to learn, contribute ideas, and help improve the way we work. We are committed to creating a supportive and inclusive workplace where employees can build their expertise, take ownership of their work, and grow alongside the organization.

PMR is an equal opportunity employer committed to providing a respectful and inclusive workplace. We offer a benefits program and an opportunity to build specialized experience within the clinical research industry while contributing to the continued success and growth of our organization.

As a Budget Specialist, you will help ensure the financial success of clinical research studies by developing, reviewing, and negotiating clinical trial budgets. Working closely with sponsors, CROs, research sites, and internal teams, you'll play an important role in bringing new clinical studies from planning to activation.

This position offers a unique opportunity to develop expertise at the intersection of finance, negotiation, and clinical research while working with a diverse portfolio of studies and stakeholders across North America and internationally. You'll contribute to improving internal processes, supporting organizational growth, and helping deliver high-quality service to our partners.

We thank all applicants for their interest; however, only those selected for further consideration will be contacted.

Job Responsibilities

Budget Management
• Review, negotiate, and finalize initial study budgets and amendments to ensure financial feasibility, compliance, and adherence to timelines
• Communicate with sponsors, external budget contacts, and sites to negotiate optimal study budgets
• Maintain a high degree of organizational skills to ensure smooth and efficient daily budget operations
• Apply strong negotiating skills to secure favorable study budget allocations
• Review sponsor budget templates and ensure alignment with internal cost standards and regulatory requirements
• Ensure all applicable study-related costs are accurately captured during the budget negotiation process
• Coordinate with Contracts team to ensure budgets alignment where applicable
• Review and monitor active sites and upcoming projects in team KPI tracker
• Update KPI tracker to ensure accuracy and workload visibility
• Coordinate with Contracts team to ensure budgets alignment where applicable
• Prioritize workload based on site activation timelines and project volume; collaborate with internal teams to ensure timely budget delivery and study startup

Operational Efficiency & Stakeholder Support
• Serve as a key point of contact for internal and external inquiries related to assigned study budgets
• Manage and respond to email communications promptly to support ongoing study operations and budget accuracy
• Reassess priorities regularly to meet the evolving demands of budget negotiations and site activations
• Assist the Budgets Team Lead in identifying and implementing process improvements to enhance efficiency and consistency
• Support onboarding and training of new team members to ensure understanding of budget processes and tools

Additional Responsibilities
• Perform other duties as assigned to contribute to the overall success of the organization’s payment and budget processes

Skills
• Clinical trial budget development, negotiation & financial analysis
• Strong understanding of study cost drivers protocol requirements & site-level budgeting considerations
• Ability to assess sponsor-proposed budgets and develop strategic counterproposals
• Stakeholder advisory support (internal teams, sponsors, external partners)
• Budget lifecycle management & tracking process optimization
• Exceptional attention to detail and financial accuracy
• Strong written and verbal communication skills
• Analytical thinking, sound judgment & confident decision-making
• Excellent organizational, prioritization & deadline management skills
• Independent work ethic with strong collaborative approach
• Adaptability in high-volume, deadline-driven environments

Qualifications
• A bachelor's degree or college diploma in Clinical Research, Health or Life Science or a related field
• A minimum of 1 year as an on-site clinical research coordinator or clinical research assistant or 2 or more years of on-site clinical research administration experience
• Experience working on or negotiating study budgets would be an asset
• Highly Proficient Microsoft Office Suite Knowledge (Excel)
• Experience with DocuSign and PDF software
• Proven ability to manage multiple projects at once
• A high level of critical and logical thinking, analysis, and/or reasoning

Working Conditions
This role is eligible for hybrid or remote work.

Test
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Monday - Friday 9:00AM-5:00PM
40

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