Clinical Operations

PharPoint Research > Services > Clinical Operations & Project Management

Tailored clinical operations & project management services

PharPoint’s clinical operations management team is experienced, innovative, and dedicated to high quality, on-time delivery. Our clinical research project management has worked with external vendors, regulatory agencies, and clinical research sites and centers within critical timelines to offer more efficient and cost-effective solutions to trial management. We provide special attention and strategic planning to support patient enrollment and retention as well as strategic site selection.

PharPoint’s project managers collaborate with your internal project team from the start to ensure that we understand your individual needs and priorities. By closely aligning our project management methodology with your team’s needs, we provide a tailored plan that meets your requirements and ensures timely communication and goal completion.


average experience of our clinical operations leadership

Why choose PharPoint Research?

Our fully integrated, multi-disciplinary team is tailored to meet the needs of your study, equipped with consistent communication and a full knowledge of study direction. We have a field-based and in-house clinical research associate (CRA) team structure, allowing us to communicate study needs and remedy obstacles as they arise.

We provide special attention and strategic planning to optimize enrollment, and proactively manage obstacles such as subject screen challenges and excessive dropouts. PharPoint provides both internal and site team training on the protocol, study implementation guidelines, and issue escalation processes to mitigate enrollment risks.

Our team identifies sites that meet enrollment expectations while focusing on subject retention. In addition to site feasibility and qualification audits, PharPoint’s industry network allows us to connect sponsors with sites we’ve had positive working relationships with in past studies.

Our comprehensive clinical research project management services include:
  • Global clinical trial project management
  • Clinical monitoring
  • Site feasibility assessments
  • Investigator meeting preparation and presentations
  • Risk mitigation
  • Study startup support
  • Site management and communication production
  • Vendor management
  • Interactive Voice Response System (IVRS) vendor selection and oversight
  • Clinical Trials Management System (CTMS)
  • Investigator grant and research budget preparation and administration
  • Study rescues

Meet a PharPoint Clinical Operations Expert

Nancy Peterson, Associate Director of Clinical Operations

Ms. Peterson has worked in the health care industry since 1989 and is highly experienced in clinical research.

Her career includes US and global experience as a CRA, project manager, business development director, and vendor manager of Phase 1-3 studies. At PharPoint, Ms. Peterson is responsible for operational oversight, periodic team performance reviews to capture best practices, continuous process improvement, and the measurement of stakeholder satisfaction.