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Clinical Monitoring Team Lead
hace 1 mes
Job Overview
As a key member of our team, you will provide leadership and guidance to the centralized monitoring team, working closely with project and clinical leads to achieve project objectives. You will be responsible for ensuring the delivery of high-quality clinical trials, while optimizing speed, quality, and cost. Your expertise will be invaluable in identifying and mitigating clinical risks, and implementing effective solutions to address them.
Key Responsibilities
- Project Oversight: Oversee clinical deliverables, manage project resources, and coordinate cross-functional project teams.
- Quality Assurance: Ensure subject safety, data integrity, and compliance with relevant regulations and guidelines.
- Communication: Establish effective project/site level communications and act as a point of contact for assigned deliverables.
- Risk Management: Identify and mitigate risks associated with project deliverables, and monitor site performance.
- Mentorship: Act as a mentor for junior staff and Technical Solution Specialists.
- Training: Support departmental training as a Subject Matter Expert.
Qualifications
- Bachelor's degree in life sciences or related field.
- Minimum of 5 years of relevant clinical trial experience.
- Formal or informal leadership experience.
- Advanced knowledge of clinical trial conduct and applicable clinical research regulatory requirements.
- Strong written and verbal communication skills.
- Ability to work on multiple projects and manage competing priorities.
- Strong organizational, problem-solving, and decision-making skills.
- Ability to work across cultures and geographies.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make a meaningful impact. Learn more at https://www.iqvia.com/
