Senior 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 Research, Clinical Trials, Drug Development, Stakeholder Engagement, Project Management, GCP, Operational Excellence, Mentoring, Budget Management, Risk Management, Quality Standards, Cross-Functional Collaboration, Process Improvements, Audit Readiness, Health Sciences, Internal Medicine

Industry

Pharmaceutical Manufacturing

Description

Job Description Summary We are seeking a Senior Clinical Study Manager to lead the operational delivery of medium to high complexity Global Medical Affairs studies, including Non-Interventional Studies, Research Collaborations, and Investigator-Initiated Trials. This role ensures excellence in planning, execution, and reporting, while maintaining compliance with quality standards and fostering cross-functional collaboration. Job Description Key Responsibilities Lead cross-functional study teams and lead study execution operations from concept to reporting. Oversee study documentation, systems, and vendor/Third Party activities activities and deliverables. Track progress, manage budgets, risks, and ensure timely reporting and disclosures. Drive process improvements and operational excellence. Ensure compliance with process standards for quality and systems, ensure audit readiness. Mentor junior team members and contribute to training initiatives. Qualifications Bachelor’s degree or higher in Life Sciences or Healthcare. 6+ years in clinical operations or project management (pharma/CRO). Strong knowledge of GCP and global clinical development. Proven leadership in matrixed environments. Excellent communication, strategic thinking, 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 cross-functional study teams and oversee study execution operations from concept to reporting. Ensure compliance with quality standards and manage budgets, risks, and timely reporting.