Job Description Summary

We’re hiring a Clinical Study Manager to lead the operational delivery of Global Medical Affairs studies—covering Non-Interventional Studies, Research Collaborations, and Investigator-Initiated Trials. You’ll manage cross-functional teams, oversee timelines and budgets, and ensure compliance with quality standards.

Job Description

Responsibilities

Lead study planning and study execution operations from concept to reporting.
Manage cross-functional teams and external vendors/third parties.
Track progress, metrics, risks, and manage study budgets.
Support documentation, systems, and process improvements.
Ensure compliance with quality standards, ensure audit readiness.
Mentor junior team members and support onboarding.
Compliance with systems and processes and audit readiness

Qualifications

Bachelor’s degree or higher in Life Sciences or Healthcare.
5+ years in clinical operations or project management (pharma/CRO).
Strong knowledge of GCP and global clinical development.
Excellent leadership, communication, and stakeholder engagement skills.
Fluent in English.

Commitment to Diversity & Inclusion:

Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Skills Desired

Building Construction, Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Hazard Identification, Health Sciences, Immunology, Intensive Care UnIT (Icu), Internal Control, Internal Medicine, Job Description, Medical Information, Organization Skills, Patient Care, Stakeholder Engagement, Tcp/Ip Protocols, Utilization Management (Um)

Clinical Study Manager – Global Medical Affairs

Job Description