Pam Jones Email & Phone Number

Remote

Apply Worldwide Clinical Trials values to support and drive the highest quality monitoring program in the mid-size CRO sector, by:• Identifying and effectively onboarding quality permanent and contract CRAs, ensuring timely training and efficient application of processes and systems• Conducting assessment visits to promote CRA skill development and share evolving best practices• Managing productivity and quality metrics through regular 1:1 meetings and real time feedback• Problem solving and serving as point of escalation to mitigate risk• Supporting CRA resourcing and utilization, including oversight to CRA study monitoring deliverables• Conducting performance appraisals, inclusive of year-round support and coaching to promote optimal outcomes for both company and personal goals

Applied ICON values to drive CRA delivery of quality service, meeting client program milestones and expectations, while achieving key metric and performance indicators.• Effectively managed and supported CRAs to ensure high performance and independent reliability with client deliverables, including stakeholder satisfaction.• Interviewed and executed new CRA on-boarding, assigning Mentors and subject matter experts to accelerate acclimation and business impact of new staff. • Set goals and assessed performance, engaging stakeholder feedback, while fostering CRA development toward career aspirations.• Collaborated with Project Resource Management team to optimize CRA alignment and utilization across sponsor programs.• Conducted regular quality oversight visits with CRAs, and, in the spirit of continuous improvement, promote monitoring best practices/efficiencies across the team.

Remote-Based, Denver, Co

Senior Oversight Clinical Project Leader (OCPL)Effectively directed CRA resources to ensure CRA performance and attainment of project deliverables.• Aligned CRAs to clinical trials and sites, based on geographic efficiencies, expertise and experience, working across regions and in collaboration with project teams and OCPL colleagues.• Functionally managed CRAs to assure pro-active planning and delivery of project and site milestones, including adherence to key metrics and performance indicators.• Actively coached CRAs on communications and strategies to build solid site and project team interfaces, fostering team work and retention across the Sanofi platform.• Co-Lead process improvements initiatives, including the development of CRA reference tools, to promote seamless integration of team members and consistency across the platform.(Note: I took a voluntary incentive package in 2018 to allow a short-term, personal hiatus from my professional career)

Remote-Based, Denver Co (Supporting Pra-Sanofi Partnership)

Actively supported a progressive CRA management model across the PRA and SANOFI partnership.• Effectively directed CRA resources to staff the monitoring of an expansive portfolio of clinical trials, across multiple therapeutic areas and trial phases. • Provided functional and quality oversight for CRA deliverables, ensuring adherence to protocol objectives as well as compliance to sponsor processes and industry regulations.• Co-Lead initiatives across the platform, aimed at streamlining processes, coupled with tool development to enhance CRA resources and accelerate productivity of new staff.

Remote-Based, Denver, Co (Dedicated To Inventiv-Allergan Partnership)

Regional Area Manager, Dedicated to ALLERGANManaged team of inVentiv CRAs and independent Contractors, remotely-based in the western region of the United States. • Planned and optimized study resources to assure delivery of ALLERGAN program objectives. • Monitored quality and productivity indicators, providing feedback and guidance to CRAs.• Supported staff development and talent alignment, completing performance evaluations.

Bridgewater, Nj (Home-Office Based)

Southern Zone Lead for North America Clinical Monitoring (2008-2010)Assistant Director/Clinical Research Manager (2001-2012) - Developed and managed remote-based, CRA (Clinical Research Associate) team to assure high quality and timely delivery of program objectives. Championed global process improvement initiatives to gain efficiency and advance to a more adaptive and risk-based monitoring approach. Liaised with Project Operations and Data Management to ensure quality and productivity standards. Collaborated with Safety and Quality Assurance departments to drive excellence in clinical trial execution.Senior CRA (1990-2001) - Monitored clinical trials in accordance with FDA Good Clinical Practices and ICH Guidelines, ensuring patient protection and trial integrity.

Golden, Co

Supported drug product testing of a radionuclide under investigation as a potential agent for epilepsy center localization in the brain.

Los Angeles, Ca (Satellite Office)

Monitored clinical trials in compliance with governing regulations to assure patient safety and trial integrity.

Denver, Co

Supported internal controls and coordinated nuclear pharmacy services and radiopharmaceutical supplies to area hospitals.

Bachelor Of Science (Bs), Zoology

Activities and Societies: Scholarship Student Athlete, Gymnastics

Nuclear Medicine Technologist, Arrt And Nmtcb Certified (Status Inactive)