Responsibilities
- Lead the planning, execution, and delivery of medium to large, multi-regional clinical studies.
- Develop and implement integrated study management plans.
- Serve as the primary liaison with sponsors.
- Set direction and objectives for cross-functional project teams.
- Partner with Business Development on bid defenses.
- Proactively identify, assess, and mitigate risks.
- Monitor project progress against timelines, budget, and quality metrics.
- Ensure financial performance by managing budgets.
Requirements
- Bachelor’s Degree in Life Sciences or a related field required; advanced degree preferred.
- Greater than 7 years of clinical research experience, including at least 4 years of project management experience.
- Proven ability to manage complex, global clinical trials and cross-functional teams.
- Strong leadership, communication, and stakeholder management skills.
- Demonstrated ability to manage budgets, timelines, and risk proactively.
Hard Skills
- clinical research
- project management
- study management plans
- risk assessment
- budget management
- timeline management
- quality metrics
Soft Skills
- leadership
- communication
- stakeholder management
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