Clinical Trial Project Manager (Boston, MA)
? Knowledge: Strong understanding of ICH guidelines, industry best practices, regulatory processes, and real-world evidence studies.
? Expertise: Proven experience managing diverse study types, including early-phase trials, late-phase trials, and both observational and interventional studies.
? Communication: Proven ability to liaise effectively with sponsors, sites, and other stakeholders, ensuring clear, professional, and proactive communication at every stage of the project.
? Training: Formal training in project management; certifications such as PMP, PRINCE2, or equivalent are a plus. Additionally, certifications specific to clinical trials, such as: - Certified Clinical Research Professional (CCRP),
- Certified Clinical Research Coordinator (CCRC),
- Certified Clinical Research Associate (CCRA),
- Certified Clinical Project Manager (CCPM) by recognized institutions. ? Leadership: Demonstrated ability to lead cross-functional teams and ensure projects are delivered on time, within budget, and to the highest quality standards.
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