Apply

Ready to go for it?

AI Apply speeds things up—apply directly if you prefer.

FREE ACCESS
5,000–10,000 jobs/day
Scoutfield Logo

See all jobs on Scoutfield

Search thousands of fresh jobs every day.

Discover
  • Fresh listings
  • Fast filters
  • No subscription required
Create a free account and start exploring right away.
IQVIA

Study Grant Manager – Sponsor Dedicated

IQVIA

. Translate clinical protocol visit assessment schedules into accurate Grant Plan and FMV cost estimations .

Posted 11/11/2026full-timeSofia • BulgariaMid-LevelSeniorWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical protocol assessment, grant planning, and cost estimation, with a strong focus on collaboration and negotiation within multidisciplinary teams. Proven ability to influence stakeholders and drive accurate forecasting in clinical research environments.

Highest-signal resume keywords
Clinical Protocol AssessmentGrant PlanningCost EstimationNegotiation SkillsInterpersonal Skills

ATS Keywords

Tailor your resume
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Cost AssessmentBudget ManagementForecasting AccuracyClinical Trial DesignProtocol Amendments
Soft Skills
Problem-SolvingDecision-MakingConflict ResolutionInfluencing Without AuthorityAdaptability
Certifications & Qualifications
Bachelor's Degree
Industry Keywords
Clinical ResearchSponsor ExperienceClinical Trial TeamsStudy Start-UpVendor Management

About the role

Key responsibilities & impact
  • Translate clinical protocol visit assessment schedules into accurate Grant Plan and FMV cost estimations
  • Lead the grant plan process and align with Study Lead, Study Start-up Lead, and Country Pharma Organizations (CPOs) for timely and accurate site contracting
  • Collaborate with Study Leaders to identify clinical/operational issues in protocol design and assess cost implications
  • Partner with Study Start-up teams, Budget Managers, and Early Trial Pricing partners to enhance forecasting accuracy
  • Provide clinical operational feedback to Clinical Trial Teams (CTTs) on study design impacts
  • Engage with CPOs and regional teams to ensure alignment on Grant Plan outputs and FMV processes
  • Negotiate centralized FMVs for IITs and local phase IV trials
  • Manage vendor relationships to ensure accurate and refined cost assessments
  • Identify productivity savings and cost avoidance opportunities
  • Compare cost estimations in light of protocol amendments
  • Utilize global/regional/country cost data to drive intelligent estimations

Requirements

What you’ll need
  • Bachelor's Degree Related field
  • 5 year relevant sponsor or clinical research organization experience
  • Good command of English
  • Strong interpersonal skills and ability to work in multidisciplinary, matrixed, and virtual teams
  • Decision-making ownership and accountability
  • Effective problem-solving, negotiation, and conflict resolution skills
  • Ability to influence without authority and adapt to evolving technologies