Study Manager – Clinical & Medical Role at GSK
GSK is hiring a Study Manager to lead and coordinate global clinical and evidence generation studies across multiple countries. This hybrid Manager Job role offers exposure to international clinical trial operations, CRO management, and regulatory compliance, providing a strong pathway for career growth in medical and clinical research. Graduates seeking Pharmacy Jobs and want to start their career in Pharmacy Careers can apply now.
Job Details
- Job Title: Study Manager
- Locations: Warsaw (Poland), Bengaluru (India), Siena (Italy), Mississauga (Canada), Poznan Grunwaldzka (Poland), Stevenage (UK)
About the Company
GSK is a global biopharma company uniting science, technology, and talent to improve the health of billions worldwide. GSK fosters an inclusive and collaborative environment, prioritizes innovation in specialty medicines and vaccines, and ensures professional growth for its employees. This manager’s job role plays a significant role in the company.
Educational Requirements
- At least 3+ years of relevant experience in a pharmaceutical or scientific environment
- Knowledge of clinical trials, drug development, and ICH-GCP regulations
- Familiarity with clinical study delivery systems, including Trial Master File standards
Key Responsibilities
- Monitor study conduct and progress; resolve and escalate risks/issues
- Draft, review, and maintain key clinical documents (Protocol, ICF, study plans)
- Coordinate meetings and collaborations with internal teams and external partners (CROs, vendors)
- Provide country-level oversight: recruitment, data completeness, deviations, regulatory compliance
- Manage study communications, action logs, and team rosters
- Oversee clinical supply and investigational product delivery
- Ensure eTMF inspection readiness and maintain high-quality study documentation
- Track budgets, change orders, and expenses; escalate issues as needed
- Contribute to Study Leadership and Central Study Teams; foster effective team dynamics
Skills Required
- Clinical trial project management and leadership
- Knowledge of ICH-GCP and global regulatory standards
- Stakeholder management and communication skills
- Budgeting and financial understanding for clinical studies
- Logical/analytical thinking, problem-solving, and attention to detail
- Experience with CTM systems and Microsoft Office tools
- Ability to manage multiple studies and priorities in a hybrid work model
Why This Job Role?
- Opportunity to lead global clinical studies with high impact
- Exposure to international regulatory standards and CRO management
- Professional growth within a renowned biopharma company
- Flexible hybrid working environment and supportive culture
- Graduates seeking Pharmacy Jobs and want to start their career in Pharmacy Careers can apply now.
