OUR EXPERT TEAM

PharPoint's senior management team

Members of our leadership team hold an average of 21 years experience in clinical research. Together with PharPoint’s founders, they leverage their expertise to anticipate challenges, provide quality solutions, and stay ahead of clinical trial deadlines.

Moya Hawkins Moya Hawkins
Senior Director of Strategic Consulting

Moya Hawkins has experience managing Phase 1 through Phase 4 clinical trials across both EDC and paper platforms, including global, multilingual Phase 3 and 4 studies.

Her database experience includes serving on EDC steering committees within several companies, application validation, and serving as a point person for the implementation of the transition from paper-based studies to EDC studies.

Ms. Hawkins has experience managing multi-country, emergency use protocol studies with special patient populations, and salvage therapy studies. She has served on a committee for the Society of Clinical Data Management, a non-profit dedicated to the advancement of clinical data management.

Amy Flynt Amy Flynt, PhD
Senior Director of Biostatistics and Strategic Consulting

Amy Flynt, PhD, joined PharPoint in its inaugural year to grow biostatistics operations.

Prior to PharPoint, her experience includes having provided FDA representation, serving as a DMC statistician, and acting as a statistical consultant.

She’s served as a lead statistician and provided statistical support for Phase 1 through 4 clinical trials, NDA submissions, and industry-sponsored registries.

Jayme Swinson Jayme Swinson, MS
Executive Director of Operations

Jayme Swinson’s experience in the CRO industry includes both statistical analysis and clinical database programming support for Phase 1 to Phase 4 clinical trials as well as patient registries.

He’s led multiple data standardization and warehousing projects, many of which comply with the industry-accepted SDTM format.

Mr. Swinson was one of the original members at PharPoint, and established and led the programming department, defining and refining standard processes across functional areas.

Alycia Olesen Alycia Olesen
Director of Data Management

Alycia Olesen’s experience includes managing both local and global Phase 1 to 4 clinical trials as well as utilizing multiple EDC platforms.

Throughout her career, she has worked across functional areas to facilitate communication and make improvements in working practices. This includes working closely with database programmers and data managers to develop and implement platform specific eCRF and data validation specifications, improving processes and communications and increasing efficiency within the data management and database programming departments.

Paul Johnson Paul Johnson
Clinical Operations Strategist

Paul Johnson’s experience includes both working in healthcare as well as in the drug development. Mr. Johnson brings extensive experience as a CRA, clinical project manager and clinical operations manager.

Throughout his career, he has developed and implemented various project management methodologies. This has included study planning, risk management and contingency plans as well as managing the execution of site monitoring, site management, and data collection.

In his previous management roles, Mr. Johnson has recommended and implemented various clinical operations performance and productivity improvements and consistently ensuring sponsor expectations were met.

Julie Robey Julie Robey
Director of Clinical Operations

Ms. Robey brings over 20 years of drug discovery and development experience, most recently as Director of Project Management for a small biotech focusing on timeline and vendor management in drug discovery.

Prior to that she held positions of increasing responsibility in clinical development services, strategic development and data management focusing in the areas of Hepatitis C, Hepatitis B, HIV, NASH, liver fibrosis, breast cancer and prostate cancer.

She has managed pre-clinical, Phase 1 – Phase 4 trials of all sizes from 1 site to over 500 sites globally.

Baker Sharpe Baker Sharpe
Director, Data Management

Baker Sharpe holds 13+ years of experience in clinical data management, spanning therapeutic areas including infectious disease, oncology, cardiovascular, and numerous others.

Before joining PharPoint, Ms. Sharpe spent 9 years in roles of increasing responsibility in the data management departments of two large CROs.

Currently, along with ensuring optimal performance of PharPoint’s data management group functions, Ms. Sharpe has worked to continuously train and develop the data management team to increase efficiencies and maintain state-of-the-art data management practices.

Karisa Satterly Karisa Satterly
Director of Business Development

Karisa Satterly’s experience in clinical research includes working across the biotech, pharma, device and CRO industries.

In her current role, Ms. Satterly leads initiatives for company growth and helps to diversify the company’s pipeline of work. Prior to PharPoint, Ms. Satterly held various roles of increasing responsibility in the data management industry including positions in business analytics, marketing, business development, and account management.

To speak with a member of our Business Development team, visit our “Contact Us” page or email our team at bizdev@pharpoint.com.

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