Clinical Project Manager
As a seasoned clinical project manager, you will lead the execution of end-to-end trial delivery. Your expertise will ensure timely, compliant, and within-budget results.
Responsibilities
- Developing and implementing comprehensive trial plans, complete with timelines, budgets, risk management strategies, and communication plans.
- Coordinating cross-functional teams, comprising clinical, regulatory, data, biostatistics, quality assurance, medical, and CROs / vendors.
- Managing monitoring visits, safety reporting, data validation, audit readiness, documentation, and final reporting.
- Overseeing the selection, onboarding, and monitoring of CROs / vendors to guarantee compliance and quality assurance.
Qualifications
Experience in clinical research, preferably in a senior CPM / Clinical Ops Lead position (Pharma or CRO).In-depth knowledge of ICH-GCP regulations, trial operations, budgeting, vendor management, and clinical systems.Strong leadership, communication, data-driven decision-making, and multi-tasking skills.Fluency in English; additional languages are advantageous.Join an innovative research environment that prioritizes quality, integrity, and speed.
Why This Role?
This Clinical Project Manager opportunity is ideal for professionals seeking a challenging and rewarding career in clinical research. With a strong focus on innovation and collaboration, our team offers a dynamic work environment that fosters growth and development.
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