Clinical Study Manager – Global Medical Affairs at Novartis

London, England, Ireland -

Full Time

Start Date

Immediate

Expiry Date

01 Feb, 26

Salary

0.0

Posted On

03 Nov, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Practices, Clinical Research, Clinical Trials, Drug Development, Health Sciences, Immunology, Internal Medicine, Stakeholder Engagement, Organization Skills, Patient Care, Hazard Identification, Job Description, Medical Information, Utilization Management, Building Construction, Intensive Care Unit

Industry

Pharmaceutical Manufacturing

Description

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) Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

Lead study planning and execution operations from concept to reporting while managing cross-functional teams and external vendors. Track progress, metrics, risks, and manage study budgets to ensure compliance with quality standards.