
Senior Clinical Trial Manager
2 weeks ago
Job Overview
We are seeking a skilled and experienced professional to lead our centralized monitoring team. As the Centralized Monitoring Lead, you will be responsible for providing leadership and oversight of clinical deliverables across all trial phases.
Key responsibilities include developing and reviewing study management plans, risk assessments, and analytics strategies. You will also be responsible for monitoring site performance, key risk indicators, and operational triggers.
In addition, you will have financial oversight including budget tracking and investigator payments. Coordination of cross-functional teams to meet project milestones is also a key aspect of this role.
Quality assurance through regular audits, documentation, and compliance checks is essential in this position. You will also be responsible for leading data review processes and ensuring audit readiness at all times.
The ideal candidate will have a minimum of 5 years of relevant experience or a medical degree with a minimum 4 years of clinical trial experience. Advanced knowledge of clinical trial conduct and skill in applying applicable clinical research regulatory requirements is also required.
Required Skills and Qualifications
- Experience in clinical trial conduct and management.
- Knowledge of Good Clinical Practice (GCP) and relevant local laws, regulations, and guidelines.
- Ability to work effectively in a team environment.
- Strong communication and interpersonal skills.
- Ability to analyze complex data and make informed decisions.
Benefits
This role offers a unique opportunity to work in a fast-paced and dynamic environment. As a member of our team, you will have access to ongoing training and development opportunities.
Others
If you are a motivated and experienced professional looking for a new challenge, we encourage you to apply. Please submit your resume and a cover letter outlining your qualifications and experience.
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