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Project Manager, Study Operations, Cronos

7+ years
Not Disclosed
10 Oct. 4, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

🏷️ Job Title: Project Manager – Study Operations, Cronos

📍 Location: Madrid, Spain (Remote/Home-based)
🕒 Employment Type: Full Time
🔢 Job ID: R1493054
📍 Additional Locations: Kansas | Mexico | Portugal | Remote | Bulgaria | Austria | Spain


🧭 Job Overview

The Project Manager (Project Lead) is a core member of the clinical trial team responsible for delivering clinical studies to meet contractual requirements. The role focuses on project delivery, productivity, quality, financial performance, and client satisfaction. Project Managers can manage their own studies and leverage therapeutic expertise and IQVIA solutions to drive operational excellence and strategic leadership with clients.


⚙️ Key Responsibilities

  • Project Planning & Execution:

    • Develop integrated study management plans with the core project team.

    • Execute clinical studies per contract, optimizing speed, quality, and cost.

    • Set objectives for core teams and sub-teams and assess performance.

    • Monitor progress against contract and proactively report to internal and external stakeholders.

  • Client & Stakeholder Management:

    • Serve as primary or backup contact with clients and vendors.

    • Participate in bid defense presentations; may lead presentations for smaller regional studies.

    • Manage project vendor activities as required.

  • Team Leadership & Development:

    • Build and lead cross-functional project teams to support milestone achievement.

    • Mentor less experienced team members and provide feedback to line managers.

  • Risk & Quality Management:

    • Identify project risks and issues; implement corrective and preventive actions.

    • Manage changes in project scope and follow change control processes.

    • Implement lessons learned and best practices.

  • Financial Management:

    • Ensure project financial success.

    • Forecast and identify opportunities to accelerate activities and revenue.

  • Organizational Contribution:

    • Adopt corporate initiatives and serve as a change advocate.

    • Collaborate across functional groups and geographies.


🎓 Qualifications

  • Education: Bachelor’s Degree in Life Sciences or related field (Required)

  • Experience:

    • 7+ years in clinical research, including ~5 years project management experience in a global, client-facing environment.

  • Skills:

    • Strong written and verbal communication in English, including presentation skills.

    • Strong problem-solving and decision-making skills.

    • Ability to lead through others, manage performance, and partner cross-functionally and with clients.


🌍 About IQVIA

IQVIA is a global leader in clinical research services, commercial insights, and healthcare intelligence, helping life sciences companies accelerate drug development and improve patient outcomes. IQVIA values diversity, inclusion, and belonging, empowering employees to bring authentic perspectives and drive innovation.

🔗 Learn more: https://jobs.iqvia.com


⚖️ Equal Employment Opportunity

IQVIA is committed to diversity, inclusion, and belonging, empowering all employees to achieve extraordinary outcomes through collaboration and innovation.


🗂️ Job Category:

📊 Clinical Project Management / Study Operations / Life Sciences / Global Clinical Trials