Our Team

Amy brings more than 16 years of clinical research experience across site operations, Clinical Trial Management Systems (CTMS), contract and budget negotiations, and global project leadership.

Amy began her career as a study coordinator supporting complex and high-acuity therapeutic areas including trauma and emergency medicine, cardiac, renal, women’s health, and neonatal research. Working within critical care settings and time-sensitive studies gave her deep insight into the realities faced by patients, families, and clinical sites, as well as the operational challenges of delivering successful trials.

Prior to moving into operational leadership, Amy managed contract and budget negotiations for a large U.S. health system, leading protocol feasibility reviews, insurance coverage analysis, financial modeling, and regulatory alignment.

At mdgroup, Amy has spent more than five years leading complex global projects and collaborating across patient services, mobile health, travel logistics, payments, and site support teams. Combining hands-on operational expertise with strategic oversight, she works closely with sponsors to deliver patient support solutions that are operationally sound, commercially viable, and centered around improving the clinical trial experience.

Stephanie brings more than 20 years of healthcare and clinical research experience. A registered nurse by background, she has developed a comprehensive understanding of clinical trials through leadership roles spanning clinical operations, research delivery, and healthcare management.

Prior to joining mdgroup, Stephanie spent more than a decade at Johns Hopkins University as a Clinical Trials Nurse and Nurse Manager, supporting the delivery of complex clinical research programs and contributing to advancements in patient care and medical innovation. She also provided consulting services to emerging medical device companies, advising on study design, research materials, and clinical trial strategy.

At mdgroup, Stephanie leads the Clinical Business Services function, overseeing Clinical Staffing, Global Logistics, Feasibility, and Vendor Management. Combining clinical expertise with operational leadership, she works closely with sponsors and internal teams to ensure services are delivered efficiently, compliantly, and with a continued focus on improving the patient and site experience throughout the clinical trial journey.

With more than 25 years of experience across nursing, clinical research, and patient services, Louise brings extensive expertise in clinical trial operations, patient-centered care, and global project delivery. Her career spans frontline clinical practice, research nursing, and senior operational leadership, providing her with a unique perspective on both patient care and clinical trial execution.

Prior to joining mdgroup in 2021, Louise held senior clinical leadership roles supporting global clinical trial operations, patient-facing services, and nurse network management. Earlier in her career, she worked as a specialist pediatric and research nurse, including roles at Great Ormond Street Hospital and other NHS trusts, gaining extensive experience in intensive care, rare diseases, complex patient populations, and clinical research. She holds an MRes in Clinical & Experimental Medicine from University College London, alongside advanced qualifications in clinical trials, pediatric intensive care, and nursing.

At mdgroup, Louise leads the delivery of global patient services programs, working closely with sponsors, CROs, patients, and cross-functional teams to ensure high-quality, patient-centered clinical trial support. Her expertise spans decentralized and home-based clinical trials, clinical governance, nurse network development, and operational excellence. Passionate about improving patient experiences and expanding access to clinical research, Louise is committed to delivering innovative solutions that help patients participate in trials safely, effectively, and with confidence.

Coming Soon

With 24 years of experience in clinical research and more than 30 years as a registered nurse, Joanne brings extensive expertise in clinical trial leadership, cardiology research, research ethics, and patient-centered clinical trial delivery. Her career spans frontline clinical practice, research nursing, trial management, and governance, providing a unique blend of clinical, operational, and ethical perspectives.

Joanne is an NMC Registered Nurse and holds qualifications in Adult Nursing, Cardiac Nursing, and Clinical Practice Teaching and Assessment. She has extensive experience managing Clinical Trials of Investigational Medicinal Products (CTIMPs), gene therapy and stem cell studies, medical device trials, and post-market registries. Her background includes more than 17 years in interventional cardiology research and senior leadership roles within the NHS, where she managed complex trial portfolios and multidisciplinary research teams. Joanne also serves as an Expert Member of the West of Scotland Research Ethics Committee and has contributed to cardiology research through published work and professional involvement with organizations including the British Cardiovascular Intervention Society.

At mdgroup, Joanne leads the delivery of decentralized clinical trial services, working closely with sponsors, CROs, sites, healthcare professionals, and patients to ensure studies are delivered safely, efficiently, and in accordance with the highest regulatory and ethical standards. Her expertise spans mobile health operations, patient safety, clinical governance, stakeholder management, and quality improvement. Passionate about making clinical trials more accessible and patient-focused, Joanne is committed to helping create flexible, compassionate research experiences that improve outcomes for patients while supporting successful study delivery.

Irvin Saranillo is an experienced healthcare professional with nearly three decades of nursing experience and extensive expertise in community-based care, home healthcare, and clinical research. Originally qualifying as a Registered Nurse in the Philippines in 1996, he later built a long and successful career in the United Kingdom, working across the NHS, private healthcare providers, and specialist homecare organizations.

Throughout his career, Irvin has developed significant expertise in delivering complex therapies within community settings, including intravenous therapies, central line management, cannulation, blood collection, growth hormone therapies, and disease-modifying treatments for multiple sclerosis. He has also supported patients across a range of therapeutic areas, including cystic fibrosis and other chronic conditions requiring specialist care outside traditional healthcare settings.

As a Clinical Manager at mdgroup, Irvin supports the delivery and ongoing development of patient-centered clinical trial services, working closely with sponsors, CROs, sites, healthcare professionals, and internal teams to ensure the successful delivery of decentralized and hybrid clinical trial programs. His extensive clinical background enables him to provide valuable insight into healthcare professional onboarding, service delivery, and operational excellence across complex studies.

Passionate about improving access to care, Irvin is committed to ensuring patients receive high-quality support throughout their clinical trial journey. He believes that successful clinical research depends on collaboration, innovation, and maintaining a strong focus on patient needs, helping to remove barriers and create a more positive experience for participants, sites, sponsors, and CROs alike.

With 11 years of experience in clinical research, Rafaela brings extensive expertise in clinical trial coordination, clinical operations, data management, and decentralized and hybrid clinical trial delivery. Her background spans Phase I–IV clinical trials, providing her with a comprehensive understanding of study execution across a wide range of therapeutic areas and trial models.

Rafaela holds a degree in Biomedical Science with a qualification in Clinical Analysis, alongside a postgraduate specialization in Clinical Research. Her experience includes site-level clinical trial coordination, clinical operations, mobile health services, and global study management. She has supported studies across therapeutic areas including oncology, hematology, nephrology, endocrinology, dermatology, rheumatology, diabetes, infectious diseases, and rare diseases. In addition to her industry role, Rafaela serves as a postgraduate lecturer at Pontifícia Universidade Católica do Paraná (PUCPR), where she teaches Decentralized Clinical Trials and Emerging Technologies within the Clinical Research and Evidence Analysis program.

At mdgroup, Rafaela manages global decentralized and hybrid clinical trial projects, working closely with sponsors, CROs, sites, healthcare professionals, and patients to ensure the successful delivery of patient-centered services. Her expertise spans mobile health operations, healthcare professional coordination, study implementation, and stakeholder communication, helping ensure services are delivered with quality, compliance, and operational excellence. Passionate about expanding access to clinical research, Rafaela is committed to improving the clinical trial experience through innovative, flexible solutions that benefit both patients and study teams.

Ahlam brings more than 18 years of healthcare experience, including over a decade dedicated to clinical research. Her background spans a wide range of care settings, from emergency medicine to pediatric care, providing her with extensive experience supporting both adult and pediatric patient populations across diverse healthcare environments.

As a Registered Nurse with a Bachelor of Science in Nursing (BSN) and a Bachelor of Arts degree, Ahlam combines clinical expertise with a strong understanding of research operations. Throughout her career, she has worked across multiple therapeutic areas, including neurology, endocrinology, respiratory diseases, cardiovascular conditions, infectious diseases, immunology, dermatology, and rare diseases.

At mdgroup, Ahlam oversees clinical operations, supporting healthcare professionals, coordinating patient-focused services, and helping ensure the delivery of high-quality clinical trial support. Working closely with patients, sites, sponsors, and CROs, she is passionate about improving access to care and making participation in clinical research as seamless as possible. She believes what sets mdgroup apart is its genuine commitment to both patients and the teams dedicated to supporting them throughout the clinical trial journey.

With seven years of experience in healthcare, patient engagement, and clinical research, Madison brings a strong background in community outreach, patient advocacy, and project coordination. Her career began in public health and the nonprofit sector, where she worked closely with the type 1 diabetes community and developed a deep understanding of the challenges patients and families face when participating in clinical research.

Madison holds a Master of Public Health and is a Certified Health Education Specialist (CHES). Her experience in community engagement and patient education has shaped her approach to creating meaningful connections with patients, helping to reduce barriers to participation and improve the overall clinical trial experience.

Over the past five years at mdgroup, Madison has led the Navigator Project Coordinator team, supporting patients, caregivers, research sites, and sponsors throughout the clinical trial journey. Working closely with her team, she helps ensure patients receive the guidance, support, and resources they need while participating in studies. Having personally experienced the impact clinical trials can have on patients and families, Madison is passionate about helping every participant feel valued, heard, and supported, contributing to the high levels of patient satisfaction and retention that define the mdgroup experience.

Helen Hanley is an experienced travel and patient services professional who has built her career around supporting patients participating in clinical trials. Beginning her journey in event coordination, she later transitioned into patient travel services before progressing through leadership roles to become Manager of the Navigator Travel team.

In her current role, Helen leads the team responsible for coordinating travel for patients and their families, ensuring they can attend clinical trial appointments with confidence and as little disruption as possible. Alongside managing the team, she works closely with patients, sites, and sponsors to deliver seamless travel logistics and provide expert support whenever unexpected challenges arise.

Helen’s expertise spans travel coordination, customer service, and team leadership. She is passionate about removing one of the biggest practical burdens patients face during clinical trial participation by ensuring every journey is carefully planned and professionally managed. She believes that what sets mdgroup apart is the genuine commitment its people have to delivering an exceptional patient experience through compassionate, personalized support.

Coming Soon

With 35 years of experience in finance and financial administration, Tracy brings extensive expertise in financial processes, reconciliation, invoicing, and administrative support. Her career includes nearly 20 years as a mortgage advisor, followed by a range of financial administration roles, providing her with a strong foundation in accuracy, compliance, and customer service.

Tracy is AAT qualified to Level 4 and has developed a broad range of financial and administrative skills throughout her career. Her attention to detail and commitment to accuracy help ensure financial processes are managed efficiently and consistently, supporting both internal teams and client requirements.

At mdgroup, Tracy supports the Travel and Clinical Services teams through financial reconciliation, invoice processing, and reporting activities. She plays an important role in ensuring travel-related reporting and financial records are accurate, helping support operational efficiency and client transparency. Passionate about teamwork and delivering high-quality support, Tracy contributes to the smooth running of services that help improve the clinical trial experience for patients, sites, sponsors, and CROs.

Coming Soon

Amanda Lee brings more than 20 years of experience in the travel industry, including 14 years supporting corporate clients with complex business travel arrangements. Her extensive background has equipped her with a strong understanding of the personalized service, attention to detail, and responsiveness required to support individuals with diverse travel needs.

As a Senior Navigator at mdgroup, Amanda coordinates travel arrangements for patients participating in clinical trials, helping create a smooth and stress-free experience throughout their journey. She works closely with patients, caregivers, sites, and internal teams to ensure travel logistics are managed efficiently and compassionately.

Amanda believes that no amount of technology can replace the value of human connection and takes pride in delivering the personalized support that helps patients feel cared for every step of the way.

Coming Soon

With 10 years of experience in the travel industry, Wendy brings extensive expertise in travel planning, customer service, and stakeholder communication. Her background includes coordinating travel arrangements for a wide range of clients, helping ensure journeys are well-organized, efficient, and stress-free.

Prior to joining mdgroup, Wendy worked with organizations including Henson Travel and AAA Travel, where she developed strong skills in travel coordination, client support, and relationship management. She holds a Bachelor of Science in Communications and a Master of Arts in Teaching, bringing a unique combination of communication, organization, and people-focused skills to her role.

At mdgroup, Wendy coordinates travel arrangements for patients and caregivers participating in clinical trials, helping remove logistical burdens and ensuring they can focus on their health and study participation. Working closely with patients, families, sites, and travel providers, she is committed to delivering a seamless travel experience while providing compassionate support throughout the clinical trial journey. Passionate about helping others, Wendy takes pride in making a positive difference for patients and their families every day.

With more than 20 years of experience in the travel industry, Randi brings extensive expertise in travel logistics, client services, stakeholder management, and complex itinerary coordination. Her background spans corporate, incentive, and leisure travel, including managing domestic and international travel arrangements, supporting VIP clients, and coordinating large-scale travel programs.

Throughout her career, Randi has developed strong expertise in travel planning, supplier relationship management, project coordination, and customer service. Her ability to navigate complex logistics, adapt to changing circumstances, and deliver seamless travel solutions enables her to support patients and caregivers with professionalism, efficiency, and compassion.

At mdgroup, Randi coordinates travel arrangements for patients and caregivers participating in clinical trials, helping to remove logistical barriers and reduce the stress associated with study participation. Working closely with patients, sites, sponsors, CROs, and travel providers, she ensures travel plans are managed smoothly and efficiently while providing responsive support throughout the journey. Having experienced the impact of a rare disease within her own family, Randi brings a deep sense of empathy to her role and is passionate about helping patients and caregivers feel supported, understood, and cared for every step of the way.

Sarmila Suppiah is an experienced clinical research professional with more than nine years of experience supporting global clinical trials across patient services, project coordination, and clinical operations. Her career has progressed through roles including Patient Service Officer, Clinical Trial Administrator, Clinical Research Associate, Global Project Navigator, and Senior Navigator, giving her a well-rounded understanding of patient-centered trial delivery. She holds a Bachelor of Science (Honours) in Biomedical Science (Medical Cell Biology).

At mdgroup, Sarmila oversees global patient support services, working closely with patients, sites, sponsors, and cross-functional teams to help deliver seamless clinical trial experiences. Alongside coordinating patient services and reimbursements, she supports project management activities, provides training and guidance to fellow Navigators, and assists with site training to ensure studies are delivered efficiently and to a consistently high standard.

Her experience spans Phase II–IV clinical trials across a broad range of therapeutic areas, including rare diseases, neurology, rheumatology, oncology, respiratory, infectious diseases, ophthalmology, and cardiology. Passionate about continuous improvement, Sarmila enjoys mentoring colleagues, solving operational challenges, and finding new ways to enhance the experience for patients and study teams. She is committed to helping reduce barriers to participation and ensuring every patient receives personalized, high-quality support throughout their clinical trial journey.

With more than 15 years of healthcare experience, Jessica brings a diverse background spanning patient care, clinical support, and healthcare administration. Her career has included roles in pediatrics, internal medicine, urgent care, nuclear medicine, laboratory management, and emergency medicine, as well as supporting families as a birth and postpartum doula.

At mdgroup, Jessica supports patients, caregivers, sites, and internal teams by coordinating reimbursement programs, facilitating mobile health visits, and helping ensure clinical trial services are delivered smoothly and efficiently. Drawing on her extensive healthcare experience, she is passionate about creating positive experiences for patients and helping remove barriers that might otherwise prevent participation in clinical research.

Jessica is particularly motivated by the opportunity to help patients and their families access clinical trials that may not have been possible without additional support. She believes what sets mdgroup apart is its genuine commitment to putting patients first and ensuring every participant feels supported throughout their clinical trial journey.

Martins brings more than 11 years of experience across healthcare support, clinical research operations, project coordination, and data management. His career combines a strong analytical background with hands-on patient care experience, giving him a unique perspective on both the operational and human sides of healthcare delivery.

Before joining mdgroup, Martins worked in healthcare support roles across hospitals, private clinics, nursing homes, and community settings, providing direct care to patients while supporting multidisciplinary healthcare teams. Earlier in his career, he held analytical positions with Maryland Global Initiatives Corporation, an affiliate of the University of Maryland Baltimore, where he supported large-scale public health programs by validating complex healthcare datasets and strengthening reporting and quality assurance processes across multiple healthcare facilities.

At mdgroup, Martins serves as a key point of contact for patients, caregivers, and study sites, coordinating patient reimbursements, travel logistics, and clinical trial support services. Holding a Master’s degree in Human Resource Management, a Diploma in Project Management, and certifications in Clinical Research Data Management, he is passionate about helping reduce barriers to participation and ensuring patients and families feel supported throughout their clinical trial journey. His combined experience in data management, patient care, and project coordination enables him to deliver both operational excellence and a patient-centered approach to clinical research.

With more than eight years of experience in project coordination, customer service, and stakeholder management, Nadia brings expertise in patient support, travel logistics, reimbursement coordination, and clinical trial services. Her background across multiple industries has helped her develop strong communication, organizational, and problem-solving skills, enabling her to effectively support patients, sites, and study teams.

At mdgroup, Nadia supports patients, sites, and study teams by coordinating services such as patient reimbursements, home health visits, and travel-related activities. Working closely with patients, caregivers, sites, and internal teams, she helps ensure services are delivered efficiently and that any challenges are resolved quickly and effectively. Passionate about reducing barriers to clinical trial participation, Nadia is committed to helping create a seamless and supportive experience for patients throughout their clinical trial journey.

Coming Soon

With more than 20 years of experience in clinical research and healthcare services, Jessica brings extensive expertise in clinical trial operations, patient coordination, project support, and stakeholder management. Throughout her career, she has supported national and international clinical studies, working closely with sponsors, CROs, investigators, sites, and patients to help ensure successful study delivery and regulatory compliance.

Jessica’s background spans clinical trial coordination, Trial Master File (TMF) management, regulatory support, study logistics, vendor management, and patient services. She has worked with a range of organizations across the clinical research industry, developing a comprehensive understanding of study operations and the importance of collaboration between all stakeholders. Her experience also includes supporting eTMF implementation projects and contributing to process improvements that strengthen document management and inspection readiness.

At mdgroup, Jessica supports patients and sites throughout the clinical trial journey, helping coordinate services including patient reimbursements, home health visits, and study logistics. Working closely with patients, vendors, sites, and internal teams, she helps ensure services are delivered efficiently while maintaining clear communication and a strong focus on the patient experience. Passionate about building relationships and finding practical solutions, Jessica is committed to helping make clinical trial participation as seamless and supportive as possible.

Dr. Waseem Siddiqui is a physician with nine years of experience spanning medicine, medical affairs, and clinical research. Before joining mdgroup, he spent six years working in medical affairs, developing expertise in project management, medical communications, and cross-functional collaboration across the healthcare industry.

As a Project Coordinator at mdgroup, Waseem works closely with patients, sites, and study teams to support clinical trial operations, including patient reimbursements and project coordination. His medical background provides valuable insight into the patient journey, helping ensure services are delivered with care, efficiency, and a clear understanding of participants’ needs.

Waseem has experience across a range of therapeutic areas, including vaccines, cardiometabolic disease, respiratory medicine, and inflammatory conditions. He enjoys helping patients navigate their clinical trial journey and is committed to making participation as smooth and accessible as possible.

Emma brings a unique combination of patient care and clinical research experience to her role at mdgroup. Beginning her career in veterinary medicine as a veterinary technician, she developed a strong foundation in patient care, communication, and attention to detail before transitioning into clinical research.

Committed to professional development within the industry, Emma holds the ACRP Certified Professional (ACRP-CP®) credential and completed the Durham Tech Clinical Research Core Competencies Program. Her background enables her to effectively support patients, sites, and study teams while navigating the complexities of clinical trial operations.

At mdgroup, Emma serves as a primary point of contact for patients participating in clinical trials, coordinating services such as patient reimbursements, mobile health visits, and ongoing study support. She is passionate about ensuring patients always have someone to turn to for guidance and assistance, while helping reduce the administrative burden on sites and supporting a positive experience for all stakeholders. Emma enjoys the collaborative nature of clinical research and is dedicated to helping make participation in clinical trials as seamless and accessible as possible.

Coming Soon

Coming Soon

With more than 15 years of clinical research experience across site operations, project management, and patient-centered trial delivery, Brittany has played an important role in the evolution and delivery of mdgroup’s patient-focused clinical trial services across a wide range of global studies. An ACRP Certified Clinical Research Coordinator since 2016, she combines strong clinical research expertise with a passion for operational excellence.

Prior to joining mdgroup, Brittany worked as a Clinical Research Coordinator at Thomas Jefferson University and the Children’s Hospital of Philadelphia, supporting research across a variety of therapeutic areas. She holds both a Master of Public Health and a Master of Health Psychology and has contributed to multiple scientific publications throughout her career. Her experience includes gene therapy, vaccines, behavioral medicine, and infectious disease research.

At mdgroup, Brittany provides senior oversight across global patient support programs and serves as an operational lead for strategic customers. Working closely with sponsors, sites, and cross-functional teams, she helps deliver patient-centered solutions that remove barriers to participation, improve study experiences, and support successful trial outcomes. Passionate about problem-solving and innovation, Brittany is committed to helping patients access potentially life-changing treatments through clinical research.

Michele Matthews brings more than 16 years of clinical research experience spanning site operations, regulatory compliance, study start-up, and global project management. Her career has provided her with a broad understanding of the clinical trial landscape, having worked across research sites, women’s health organizations, CROs, and patient-focused clinical trial support services.

Michele began her career at a Phase I research clinic, where she served as both a Study Coordinator and Regulatory Associate before progressing into leadership roles managing clinical research teams. She later supported regulatory and compliance activities for women’s health research organizations before moving into study start-up management at the CRO level. These experiences provided her with extensive expertise in protocol review, informed consent documentation, regulatory requirements, and study activation processes across the United States and Canada.

As a Senior Global Project Manager at mdgroup, Michele oversees the delivery of complex global clinical trial programs, ensuring projects remain aligned with study protocols, timelines, budgets, and client expectations. She works closely with sponsors, CROs, sites, patients, and caregivers to support seamless study execution while helping remove barriers to participation through patient-centered solutions.

Her therapeutic area experience includes diabetes, hypertension, Alzheimer’s disease, device studies, and early-phase clinical research. Drawing on experience gained across multiple functions and organizations, Michele brings a practical, collaborative approach to project delivery and is passionate about making clinical research more accessible for patients and caregivers worldwide.

Committed to improving the clinical trial experience for all stakeholders, Michele believes that thoughtful planning, strong partnerships, and patient-focused innovation are essential to the success of modern clinical research.

Akzhan brings more than 11 years of project management experience, including seven years dedicated to clinical trials and patient support services. With a strong background in leading complex global projects, she has extensive experience managing cross-functional teams, overseeing project budgets, mitigating risks, and ensuring successful delivery across diverse stakeholder groups.

Holding an MBA, Akzhan combines strategic project leadership with a deep understanding of clinical trial operations. Throughout her career, she has supported studies across a wide range of therapeutic areas, including oncology, neurology, autoimmune diseases, and rare diseases, working across Phase I through Phase IV clinical trials. Her expertise includes stakeholder management, financial oversight, resource planning, and delivering operational efficiencies that support both study performance and patient outcomes.

At mdgroup, Akzhan manages global projects that provide critical support services to patients, sites, sponsors, and CROs. Working closely with internal teams, external partners, and study stakeholders, she helps ensure services are delivered efficiently, compliantly, and with a continued focus on patient well-being. She is particularly passionate about the human side of clinical research and believes that providing meaningful support throughout the patient journey is essential to improving both the clinical trial experience and study success.

Primula brings more than eight years of clinical research experience spanning site operations, decentralized clinical trials (DCT), project management, and study start-up. Her career has provided a broad perspective on the clinical research landscape, having worked across multiple stages of the trial lifecycle, from patient recruitment and site support through to global project delivery and study implementation.

She began her clinical research career at Duke Cancer Institute as a Clinical Research Coordinator, supporting epidemiological research and investigational product development. She later joined IQVIA, where she held roles as a Senior Virtual Study Coordinator and Clinical Project Manager, supporting decentralized clinical trials and study platform development. Prior to joining mdgroup, Primula served as a Global Project Manager, overseeing mobile health clinical trial programs from study start-up through closeout. She also holds a Master’s degree in Psychology with a research focus.

At mdgroup, Primula leads study start-up activities, supporting protocol review, study documentation development, system setup, and cross-functional collaboration to ensure studies are positioned for successful delivery. Her experience spans a wide range of therapeutic areas, including oncology, neurology, immunology, infectious diseases, cardiology, dermatology, gastroenterology, and nephrology. She is passionate about creating efficient study foundations that reduce burden for patients, sites, sponsors, and CROs while supporting successful clinical trial outcomes.

With nine years of experience in clinical research, clinical operations, and project management, Judy brings extensive expertise in supporting global clinical trials from study start-up through closeout. Her background spans clinical trial management, decentralized research models, site operations, financial management, and strategic project leadership.

Prior to joining mdgroup, Judy held roles with organizations including Merck Pharmaceuticals, Accenture, Care Access, Greenphire, and the University of Pennsylvania. Her experience spans oncology, cystic fibrosis, OB/Gyn, neonatology, cardiology, autoimmune diseases, endocrinology, and ophthalmology, providing her with a broad understanding of clinical research across site, vendor, CRO, and sponsor environments. She holds a Master of Business Administration (MBA), a Bachelor of Science in Biology, and is a certified Project Management Professional (PMP).

At mdgroup, Judy works closely with clients, research sites, and internal teams to coordinate project activities, resolve operational challenges, and ensure the successful delivery of patient support services. Passionate about continuous improvement and collaboration, she is committed to creating efficient, well-coordinated study operations that enhance communication, improve stakeholder experiences, and support successful clinical trial outcomes.

Audrey McGuire brings more than eight years of experience across clinical research, precision medicine, and project management. She began her career supporting oncology and precision medicine programs before moving into clinical operations, where she managed complex research initiatives and cross-functional teams. Prior to joining mdgroup, Audrey held project and clinical operations roles at Tempus AI and CPC Clinical Research, gaining extensive experience in study execution, operational strategy, regulatory compliance, and stakeholder management. She holds a Master of Public Health (MPH).

As a Global Project Manager at mdgroup, Audrey leads the delivery of global patient support programs for international clinical trials. Working closely with sponsors, CROs, research sites, and cross-functional teams, she oversees study start-up, implementation, financial management, operational forecasting, risk mitigation, and the delivery of patient travel, reimbursement, stipend, concierge, and mobile health services. Her collaborative approach helps ensure studies are delivered efficiently while providing an exceptional experience for patients and sites.

Audrey is passionate about improving access to clinical research by reducing the logistical and financial barriers that can prevent participation. She enjoys solving complex operational challenges and developing practical, patient-centered solutions that improve study delivery and strengthen client partnerships. She believes mdgroup stands apart by acting as a true extension of its clients’ teams, combining flexibility, responsiveness, and personalized support to help sponsors and CROs deliver successful clinical trials while keeping patients at the heart of every study.

With 24 years of experience in clinical research, Chrystelle brings extensive expertise in clinical trial management, project leadership, and global study delivery. Her career has spanned a wide range of clinical research roles, progressing from Clinical Project Assistant and Clinical Trial Assistant through to Clinical Research Associate, Clinical Trial Manager, and Clinical Project Manager, providing her with a comprehensive understanding of the clinical trial lifecycle.

Prior to joining mdgroup, Chrystelle spent more than a decade at LFB Biotechnologies, managing international Phase I, II, and III clinical studies across therapeutic areas including oncology, rare diseases, and blood-derived products. Her experience includes study start-up and oversight, CRO and laboratory management, investigator meetings, monitoring activities, investigational product management, and cross-functional stakeholder coordination. Having previously worked on the sponsor side, she brings valuable insight into the operational and strategic challenges faced by clients. Beyond clinical research, she also co-founded and led a successful sustainable retail business, further strengthening her leadership, business management, and customer-focused expertise.

At mdgroup, Chrystelle manages global clinical trial projects, working closely with sponsors, CROs, sites, healthcare professionals, and patients to ensure services are delivered in line with study requirements, timelines, quality standards, and client expectations. Passionate about collaboration and relationship-building, she is committed to creating positive experiences for all stakeholders while helping ensure successful study outcomes. Guided by empathy and a solutions-focused approach, Chrystelle works to support patients, sites, and clients through every stage of the clinical trial journey.

Idong Gerris-Ekandem brings more than 20 years of experience across the clinical research industry, having worked on both the sponsor and CRO sides of clinical development as well as within specialist service organizations. Her broad background spans data management, pharmacovigilance, central laboratory project management, clinical monitoring, and clinical operations, providing her with a comprehensive understanding of the clinical research lifecycle.

Holding both a Master of Science in Clinical Research Administration and a Master of Public Health, Idong combines operational expertise with a strong focus on patient-centered clinical research. Her experience includes women’s health, rare diseases, and hematology, alongside extensive work in project management, stakeholder engagement, regulatory compliance, and process improvement.
As a Start Up Project Manager at mdgroup, Idong plays a key role in the early stages of clinical trial delivery, developing study documentation and operational materials that support the successful implementation of patient-focused services. She works closely with sponsors, CROs, sites, healthcare professionals, and vendors to ensure study requirements are translated into clear, compliant, and practical resources that support both patients and research teams.

Having worked across sponsor, CRO, and vendor environments, and lived in Europe for more than two decades, Idong brings a global perspective and a collaborative approach to every project. She is passionate about reducing the burden of clinical trial participation by helping create accessible, patient-friendly processes and materials that support a better experience for patients, sites, and study teams alike.

With 10 years of experience in healthcare administration and five years in clinical research, Kathryn brings a strong background in patient advocacy, healthcare operations, and study start-up activities. Her experience combines an understanding of the healthcare system with expertise in clinical trial documentation, project coordination, and process improvement.

Kathryn holds an MBA in Healthcare Administration and a Bachelor’s degree in Health Sciences. Prior to moving into clinical research, she worked in healthcare administration as a Prosthetic-Orthotic Fitter and Billing Administrator, gaining valuable insight into patient needs, healthcare processes, and navigating the complexities of the U.S. healthcare system.

At mdgroup, Kathryn is responsible for developing and managing study documentation, translating clinical trial protocols into operational materials that support successful service delivery. Her expertise in project coordination, cross-functional collaboration, and process improvement helps ensure studies are set up efficiently and accurately. Passionate about patient advocacy and operational excellence, Kathryn is committed to supporting high-quality clinical trial experiences that benefit patients, sites, sponsors, and CROs alike.

Coming Soon

Coming Soon

Rohini Akosa brings more than 30 years of healthcare experience, including 15 years in clinical research and two decades in nurse management, healthcare recruitment, procurement, and operational leadership. A Registered Nurse by background, she qualified at St Mary’s Hospital, Paddington, before building an extensive career across clinical research organizations, healthcare providers, and recruitment services. Her experience includes research nursing, clinical study coordination, compliance, healthcare staffing, and business management. She holds a BA (Hons) in Business Management and a Postgraduate Diploma in Human Resource Management (CIPD).

As Head of Vendor Management at mdgroup, Rohini leads the development and management of the company’s global network of healthcare professionals and mobile health vendors, ensuring patients receive high-quality clinical support wherever they are in the world. Working closely with project managers, clinical teams, and international partners, she oversees vendor selection, performance, and operational readiness to deliver reliable healthcare professional coverage across decentralized and hybrid clinical trials, including in geographically complex and hard-to-reach regions.

Rohini’s expertise spans clinical trial coordination, healthcare procurement, vendor management, compliance, and workforce planning across a wide range of therapeutic areas, including neurology, vaccines, rheumatology, rare diseases, and advanced imaging studies. She is passionate about building long-term partnerships with healthcare professionals around the world and believes strong collaboration, clinical excellence, and flexible patient-focused solutions are essential to improving access to clinical research and delivering successful studies for sponsors, CROs, research sites, and patients alike.