Site & Patient Services

Flexible site & patient support anywhere you need it

Enhancing Site Performance and Patient Engagement

ProPharma’s Site & Patient Services function as an extension of the site team, combining experienced personnel, standardized processes, and enabling technology to deliver reliable, compliant support globally. The result: faster start-up, expedited enrollment, improved retention, smoother visits, and better patient experiences in traditional, hybrid, and decentralized clinical trials (DCTs).

By integrating site, patient, and operational support into one coordinated model, we reduce the administrative and logistical challenges that often slow studies down. Our teams adapt to each protocol and region, assist with high-impact activities such as pre-screening, patient communication, and home health visits, and ensure sites have the resources and guidance needed at every stage. This flexible framework allows sponsors to improve efficiency, enhance participant engagement, and maintain quality no matter where the trial is conducted or how complex the study design.

healthcare-provider-working-on-tablet-device-ss-1849836292-650x425

Our Core Differentiators 

Regulatory Sciences icon

Flexible Resourcing for Clinical Sites

  • On-site and remote clinical trials resourcing options
  • Registered Nurses, Clinical Research Coordinators, and Research Assistants
  • Specialty roles including Phlebotomists, Dieticians, LPNs, Data Managers, and more
  • Scalable support through ProPharma’s global network of clinical research professionals
Patient support programs icon

Customized Support for Patient-Centric Clinical Trials

  • Solutions tailored to the unique needs of each study and clinical site
  • Expand capacity by supplementing existing teams
  • Enhance patient centricity in clinical trials with better engagement, compliance, and retention
  • Support models for both traditional, hybrid, DCT and virtual clinical trial
Computer System Validation icon

Streamlined Clinical Trial Technology

  • Clinical Trial Management System (CTMS) for site activity tracking
  • eSource, eConsent, and Telehealth tools to support remote clinical trials and virtual clinical trial participation
  • Reduce administrative burden while improving patient and site experience

Specialized Delivery Teams

Smiling doctor young man meeting exam-room

Site Support Team

Boost Site Performance with ProPharma’s Site Support Team

ProPharma empowers your sites to do more – without adding burden. Acting as a true extension of the site, our team provides seamless coordination and a single point of contact for sponsors, ensuring consistency and efficiency across regions.

With trained research professionals embedded in your study, with remote and on-site options, we handle the details that matter most: resourcing, onboarding, and day-to-day operational support. Our team can support your sites at every step of the study process starting from patient recruitment and pre-screening to data entry and visit reminders, we help sites stay focused on what counts – delivering exceptional patient care and driving study success.

Home Health Team

Your Partner in Seamless Home Health for Clinical Trials

At ProPharma, we make decentralized trials simple, reliable, and patient-focused. Our integrated team of experts works behind the scenes to ensure every home visit is delivered with precision and care – from study start-up to final patient interaction.

We combine global coordination, clinical oversight, and highly trained, employee clinicians to bring the trial experience directly to patients’ homes. This means fewer site visits, greater convenience, and improved retention, without compromising compliance or quality.

From initial planning and documentation to scheduling and execution, our process is designed to keep studies on track and patients engaged. With ProPharma, sponsors gain a trusted partner who understands the complexity of home health services and delivers solutions that work.

Healthcare provider writing on clipboard while attending to a patient

Real World Evidence: ProPharma’s Team Sets the Standard in Home Health

ProPharma differentiates our home health/DCT offering through execution and commitment. This biotech company has used many home health vendors over the past ten years and they have felt the difference working with the ProPharma DCT team.

"Wish to thank you and your team for the simply superlative work you have done. You have been the champions for this study, and time and time again, you all have come through successfully through thick and thin."

Medical Director
Biopharmaceutical Customer

Real World Evidence: ProPharma’s Team Sets the Standard in Home Health

ProPharma differentiates our home health/DCT offering through execution and commitment. This biotech company has used many home health vendors over the past ten years and they have felt the difference working with the ProPharma DCT team.

"Wish to thank you and your team for the simply superlative work you have done. You have been the champions for this study, and time and time again, you all have come through successfully through thick and thin."

Medical Director
Biopharmaceutical Customer

Health care worker showing patient something on mobile phone

Technology Enablement

Our clinical trial technology ecosystem supports both clinical research sites and patients through:

  • CTMS for clinical research trial management and resource tracking
  • eSource for decentralized data capture
  • eConsent for clinical trials with audit trails and re-consent alerts
  • Telehealth capabilities to connect investigators, site teams, and patients in remote clinical trial workflows

Why Sponsors Choose Us

We act as an extension of the clinical site, combining global resources with local expertise. Our teams support both remote clinical trials and on-site operations, ensuring patients remain at the center of every study.

Increase Site Capacity

Strengthen clinical site operations with flexible support that eases workload, reduces bottlenecks, and helps teams focus on higher-value study activities.

Prioritize Patient Experience

Enhance engagement and retention through tailored, patient-centric models that meet participants where they are.

Accelerate Study Timelines

Accelerate timelines with remote clinical trials, virtual clinical trials, and advanced clinical trial technology.

GoClinical System

Designed for streamlined success.

21 CFR Part 11 and GDPR web-based eSource application

Accessible via mobile device or desktop browser.

Why GoClinical?

  • Record and submit source data in real time
  • Reduce source turnaround times and allow for faster data entry in EDC
  • Reduce documentation errors
  • Improve PI oversight and safety

Customizable per protocol and visit procedures

  • Source forms are designed during study set-up and approved by Sponsor prior to implementation
  • Able to include job requisition form upload
  • Each record includes an audit trail

Role-based access with distinct UI and permissions for each role

  • GoClinical Clinician (GCC)
  • ProPharma Reviewer
  • Site Staff

Whether you’re running traditional, hybrid, DCT, remote clinical trials, or virtual clinical trials, ProPharma helps you strengthen your clinical sites, engage patients, and leverage leading clinical trial technology to deliver results.

Our Site & Patient Services Experts

  • Shelby Stillwagon Bio Photo

    Shelby Stillwagon

    Vice President, Decentralized Clinical Trials

    View Bio

  • Amy Scalise Bio Photo

    Amy Scalise

    Associate Director, Decentralized Clinical Trial Management

    View Bio

Shelby started her career in academic research, then moved to the clinical site environment, working in oncology, and has spent the past 11 years focused on supporting and operationalizing Site & Patient Services. Since 2013, Shelby has worked with numerous sponsors across hundreds of clinical trials, where she has provided expert guidance on decentralized visit design and logistics. She has held multiple oversight roles, supporting global teams across a wide variety of therapeutic areas including rare disease, pediatrics, oncology, neurology, and infectious diseases. Her expertise lies in collaborating with involved stakeholders to build and maintain study-specific, quality-focused processes that support complex decentralized clinical trials.
Amy began her career in the industry more than 15 years ago as a clinical research nurse and has progressively advanced to leadership roles. She has been instrumental in the initiation, planning, and management of numerous clinical trials across various therapeutic areas.

For the past 12 years, her focus has been on Site & Patient Services, providing expert guidance and operational support for studies in oncology, neurology, rare diseases, and infectious diseases. She has overseen global teams, ensuring the implementation of study-specific processes that meet regulatory requirements and maintain high-quality standards. Amy excels in stakeholder collaboration, training, and protocol development, supporting the successful execution of complex decentralized clinical trials. Her dedication to excellence ensures that all aspects of study management are meticulously handled, from project planning to regulatory compliance.

News & Insights

Preparing for eCTD 4.0: What FDA Submitters Need to Know

January 29, 2026

Preparing for eCTD 4.0: What FDA Submitters Need to Know

eCTD 4.0 is coming. Learn what’s changing, why early planning matters, and how FDA submitters can prepare for a smooth transition.

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outsourcing, and Quality Assurance

January 26, 2026

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outs...

Discover how pharmaceutical and biotech companies can elevate laboratory compliance in 2026 through GLP, strategic outsourcing, and robust quality assurance.

2025 Year in Review: Regulatory Shake-Ups Reshaping Pharma Promotion in 2026

January 14, 2026

2025 Year in Review: Regulatory Shake-Ups Reshaping Pharma Promotion in 2026

Explore 2025's FDA enforcement trends, OPDP changes, and evolving guidance shaping pharma advertising, MLR review, and compliance strategies for 2026.

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero Targets

January 27, 2026

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero T...

ProPharma’s greenhouse gas reduction targets are validated by SBTi, aligning with the Net-Zero Standard and a commitment to reach net-zero by 2050.

ProPharma Expands Operations with New Office in Hyderabad

December 11, 2025

ProPharma Expands Operations with New Office in Hyderabad

ProPharma expands with a new office in Hyderabad, enhancing innovation and growth in regulatory, clinical, and compliance services for the life sciences industry.

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

December 4, 2025

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

ProPharma taps Daniel Ryan as President of Clinical Research Solutions, strengthening its clinical trial management leadership and expanding its FSP Solutions.

ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Case Study High-Volume Global Pharmacovigilance Onboarding - ProPharma

January 30, 2026

High-Volume Global Pharmacovigilance Onboarding

A global biotechnology sponsor faced a sudden surge in pharmacovigilance demand, with monthly ICSR volumes exceeding 30,000 cases across multiple regions. Limited internal capacity, tight onboarding...

Case Study Stabilizing High-Volume Legal Case Processing Through Structured Governance - ProPharma

January 28, 2026

Stabilizing High-Volume Legal Case Processing Through Structured Governance

ProPharma’s client faced escalating operational risk as high-volume legal case documentation overwhelmed their prior vendor. Thousands of documents, missed regulatory timelines, and a surge of...

Case Study Overcoming Operational Hurdles in a High-Stakes Stroke Trial - ProPharma

December 15, 2025

Overcoming Operational Hurdles in a High-Stakes Stroke Trial

Argenica Therapeutics’ Phase 2 acute ischaemic stroke trial faced the challenges of unpredictable patient presentation, narrow treatment windows, and demanding emergency care environments. This...

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

March 12, 2026

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

Uncover the intricacies of Pharmacovigilance System Master File (PSMF) management and explore proven strategies to ensure inspection readiness, effective MAH oversight, and regulatory compliance...

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

February 17, 2026

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

With promotional scrutiny increasing around areas such as social media, influencer campaigns, direct-to-consumer (DTC) messaging, and data-driven claims, the session walks through the characteristics...

Scaling High-Quality Medical Information Through Offshoring

February 11, 2026

Scaling High-Quality Medical Information Through Offshoring

Navigate the complexities of offshoring Medical Information and explore proven strategies to ensure consistent quality, regulatory compliance, and seamless global execution. Join us for an...

News & Insights

Preparing for eCTD 4.0: What FDA Submitters Need to Know

January 29, 2026

Preparing for eCTD 4.0: What FDA Submitters Need to Know

eCTD 4.0 is coming. Learn what’s changing, why early planning matters, and how FDA submitters can prepare for a smooth transition.

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outsourcing, and Quality Assurance

January 26, 2026

Elevating Laboratory Compliance in 2026: How Pharma & Biotech Navigate GLP, Outs...

Discover how pharmaceutical and biotech companies can elevate laboratory compliance in 2026 through GLP, strategic outsourcing, and robust quality assurance.

2025 Year in Review: Regulatory Shake-Ups Reshaping Pharma Promotion in 2026

January 14, 2026

2025 Year in Review: Regulatory Shake-Ups Reshaping Pharma Promotion in 2026

Explore 2025's FDA enforcement trends, OPDP changes, and evolving guidance shaping pharma advertising, MLR review, and compliance strategies for 2026.

Previous Post Arrow Next Post Arrow
ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero Targets

January 27, 2026

ProPharma Sets the Gold Standard in Sustainability with SBTi-Approved Net-Zero T...

ProPharma’s greenhouse gas reduction targets are validated by SBTi, aligning with the Net-Zero Standard and a commitment to reach net-zero by 2050.

ProPharma Expands Operations with New Office in Hyderabad

December 11, 2025

ProPharma Expands Operations with New Office in Hyderabad

ProPharma expands with a new office in Hyderabad, enhancing innovation and growth in regulatory, clinical, and compliance services for the life sciences industry.

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

December 4, 2025

ProPharma Welcomes Dan Ryan as President of Clinical Research Solutions

ProPharma taps Daniel Ryan as President of Clinical Research Solutions, strengthening its clinical trial management leadership and expanding its FSP Solutions.

Previous Post Arrow Next Post Arrow
ProPharma Recognized for AI Excellence at ECCCSA

January 31, 2025

ProPharma Recognized for AI Excellence at ECCCSA

ProPharma wins Silver at ECCCSA for AI innovation in Medical Information, enhancing efficiency and quality in delivering accurate medical information.

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

October 9, 2024

ProPharma Receives 2024 CPHI Regulatory and Compliance Award

ProPharma wins CPHI Pharma Award for excellence in regulatory and compliance innovation, enhancing efficiency and accelerating market access for life-saving therapies.

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

September 24, 2024

ProPharma Honored in the 2024 Clinical Trials Excellence Awards

ProPharma honored with Clinical Trials Excellence Award 2024, recognizing their outstanding contributions in the pharmaceutical industry.

Previous Award Arrow Next Award Arrow
Case Study High-Volume Global Pharmacovigilance Onboarding - ProPharma

January 30, 2026

High-Volume Global Pharmacovigilance Onboarding

A global biotechnology sponsor faced a sudden surge in pharmacovigilance demand, with monthly ICSR volumes exceeding 30,000 cases across multiple regions. Limited internal capacity, tight onboarding...

Case Study Stabilizing High-Volume Legal Case Processing Through Structured Governance - ProPharma

January 28, 2026

Stabilizing High-Volume Legal Case Processing Through Structured Governance

ProPharma’s client faced escalating operational risk as high-volume legal case documentation overwhelmed their prior vendor. Thousands of documents, missed regulatory timelines, and a surge of...

Case Study Overcoming Operational Hurdles in a High-Stakes Stroke Trial - ProPharma

December 15, 2025

Overcoming Operational Hurdles in a High-Stakes Stroke Trial

Argenica Therapeutics’ Phase 2 acute ischaemic stroke trial faced the challenges of unpredictable patient presentation, narrow treatment windows, and demanding emergency care environments. This...

Previous Resource Arrow Next Resource Arrow
Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

March 12, 2026

Mastering the PSMF: The Pillar of Inspection Readiness for MAHs, LPPVs & QPPVs

Uncover the intricacies of Pharmacovigilance System Master File (PSMF) management and explore proven strategies to ensure inspection readiness, effective MAH oversight, and regulatory compliance...

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

February 17, 2026

Evolving FDA Expectations: How High-Functioning MLR Teams Manage Risk in 2026

With promotional scrutiny increasing around areas such as social media, influencer campaigns, direct-to-consumer (DTC) messaging, and data-driven claims, the session walks through the characteristics...

Scaling High-Quality Medical Information Through Offshoring

February 11, 2026

Scaling High-Quality Medical Information Through Offshoring

Navigate the complexities of offshoring Medical Information and explore proven strategies to ensure consistent quality, regulatory compliance, and seamless global execution. Join us for an...

Previous Webinar Arrow Next Webinar Arrow