Global Study Manager position supporting delivery of clinical trials from protocol development through close-out in a sponsor-dedicated model. The role involves collaborating with cross-functional global teams to ensure studies meet timelines, budgets, and compliance standards, with focus on cardiovascular research programmes.
Responsibilities
- Support clinical study delivery from protocol development through study close-out and archiving
- Collaborate with internal stakeholders, CROs, and external vendors on global studies
- Ensure studies are delivered on time, within budget, and meet quality and compliance standards
- Support innovative programmes including global cardiovascular clinical trials
Requirements
- Degree in Life Sciences, Medical Sciences, Biological Sciences, or related field
- 3+ years global trial management experience in clinical research, pharmaceutical, biotechnology, or CRO
- Strong understanding of clinical development and drug development processes
- Comprehensive knowledge of ICH-GCP and global clinical trial regulations
- Proven project management and organisational skills
- Strong stakeholder management and communication abilities
- Experience working in global cross-functional teams
Compensation: Competitive base salary and performance related incentives
Vacancy posted more than 2 months ago
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