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Clinical Project Manager IRR ISCS RWE

Ref: 613144

Alpharetta, United States

$145,000

  • Permanent
  • Project Management Expert
  • Clinical Trials Leadership
  • Risk And Compliance Management

About the candidate

The candidate brings comprehensive experience as a Clinical Project Manager with a focus on IRR, ISCS, and RWE, currently engaged in overseeing various clinical trials. With a background rooted in significant roles within sectors related to healthcare and clinical research, the candidate has demonstrated proficiency in managing complex projects that adhere to SOPs, policies, and practices. They have been pivotal in the realms of project finance, risk mitigation, and clinical trial oversight across national and global levels.

Armed with a solid educational foundation in public health and several certifications including PMP and Lean Six Sigma, they excel in streamlining processes and ensuring compliance with clinical standards. Their contributions have consistently led to improved productivity, quality deliverables, and strategic alignment with overarching program goals.

What makes them great?

  • Efficiency Improvements: Played a key role in the implementation of CTMS systems leading to increased productivity and compliance with regulatory requirements.
  • Budget and Resource Optimization: Successfully managed projects with significant budgets, ensuring optimal use of resources without compromising on quality.
  • Strategic Leadership: Consistently ensures that all project activities align with strategic objectives, enhancing overall project success and stakeholder satisfaction.

Areas of expertise

  • Project Management Skills: Demonstrated expertise in managing timelines, quality, and deliverables for clinical projects ensuring high levels of patient and customer satisfaction.
  • Risk and Compliance Management: Proficient in assessing and managing risks while ensuring all operations are compliant with necessary guidelines and standards.
  • Financial Oversight: Extensive experience with budgeting, feasibility analyses, and maintaining financial integrity across clinical trials.