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IQVIA

Senior Clinical Project Manager

IQVIA

. Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies .

Posted 10/16/2026full-timeUnited StatesSenior💰 $93,100 - $232,800 per yearWebsite

Core Competencies

Role fit
Core Competencies

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

Demonstrates expertise in leading multi-regional clinical studies, managing complex global clinical trials, and fostering strong client relationships. Proficient in project management, budget oversight, risk mitigation, and mentoring team members.

Highest-signal resume keywords
Clinical Research ExperienceProject Management ExperienceLeadership SkillsStakeholder ManagementBudget Management

ATS Keywords

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Applicant Tracking System Keywords

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

Hard Skills
Clinical Study ManagementRisk AssessmentIssue ResolutionChange Control ProcessesTimeline Monitoring
Soft Skills
Communication SkillsMentoring SkillsCollaboration Skills
Industry Keywords
Life SciencesCardiovascular TherapeuticsRenal TherapeuticsMetabolic Therapeutics

About the role

Key responsibilities & impact
  • Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies
  • Develop and implement integrated study management plans
  • Serve as the primary liaison with sponsors and manage client relationships
  • Set direction and objectives for cross-functional project teams
  • Partner with Business Development on bid defenses and contribute to winning new business
  • Identify, assess, and mitigate risks; lead issue resolution and corrective and preventative action plans
  • Collaborate with internal functional groups to support study execution
  • Monitor project timelines, budgets, and quality metrics
  • Manage budgets, forecast revenue, and identify opportunities to accelerate delivery
  • Manage scope changes and oversee change control processes
  • Promote continuous improvement by sharing lessons learned and best practices
  • Mentor junior team members and contribute feedback on team performance

Requirements

What you’ll need
  • Bachelor’s Degree in Life Sciences or a related field required; advanced degree preferred
  • Greater than 7 years of clinical research experience
  • At least 4 years of project management experience
  • Equivalent combination of education, training, and experience may qualify
  • Proven ability to manage complex, global clinical trials and cross-functional teams
  • Strong leadership, communication, and stakeholder management skills
  • Demonstrated ability to manage budgets, timelines, and risk proactively
  • Experience leading bid defenses and client engagements is preferred
  • Experience in Cardiovascular, Renal, and Metabolic therapeutics

Benefits

Comp & perks
  • Health and welfare benefits
  • Incentive plans, bonuses, and/or other forms of compensation may be offered