On-Site Monitoring
Site visits assess protocol adherence, source documentation, investigational product accountability, informed consent, and essential records while supporting research teams with timely findings and practical follow-up.
Keep your clinical programme moving with flexible on-site, remote, and risk-based monitoring tailored to study priorities. DRK Research Solutions combines proactive site oversight, focused data review, and clear sponsor communication to protect participant safety, data integrity, and protocol compliance. Our global operational network supports Phase II–IV studies with practical monitoring strategies that help teams identify issues early and maintain momentum through closeout.

Flexible operational oversight designed to safeguard trial quality, compliance, timelines, and participant well-being across study phases.
Site visits assess protocol adherence, source documentation, investigational product accountability, informed consent, and essential records while supporting research teams with timely findings and practical follow-up.
Centralized review of clinical and operational data helps identify emerging trends, discrepancies, and site needs without waiting for an on-site visit, enabling responsive oversight.
Monitoring plans prioritize critical data, processes, and sites according to study risk, helping sponsors focus resources where oversight can have the greatest impact.
Support site identification, feasibility, initiation, ongoing coordination, and issue resolution to help investigative teams remain prepared, engaged, and aligned with protocol requirements.
Ongoing data review, discrepancy management, medical coding, SAE reconciliation, and vendor reconciliation help maintain accurate, consistent, and analysis-ready clinical datasets.
Finalize monitoring and data activities through issue resolution, database review, audit support, lock documentation, standards conversion, archival, and site closure coordination.
Every study needs oversight that matches its design, sites, data flows, and risk profile. DRK Research Solutions blends on-site verification with remote and centralized review to help sponsors concentrate attention on critical data and participant protections. From site activation through closeout, our monitoring support connects clinical operations, data management, safety, and project teams for timely escalation, documented follow-through, and inspection-ready trial conduct.

Integrated clinical expertise and accountable support for complex, multi-regional study delivery.
Worldwide operational networks pair broad study capability with localized proficiency across diverse research environments.
Experienced teams support multi-regional trials from planning through closeout, with focused operational oversight.
Clinical operations, data management, safety, and regulatory capabilities align around shared study objectives.
Participant well-being and access to innovative therapies remain central to every monitoring decision.
Clinical, scientific, and operational leaders focused on reliable study delivery.

Executive Director
Dr. Shahab Q. Khokhar serves as Executive Director at DRK Research Solutions SA, bringing strategic leadership and deep pharmaceutical expertise to the organization's global operations. With a career rooted in clinical research and pharmaceutical development, Dr. Khokhar has been instrumental in shaping DRK's growth from a Patient Advocacy Organization into a full-service CRO and CDMO. He provides executive oversight across multi-regional clinical trials, regulatory compliance, and business strategy, ensuring the company upholds the highest GxP and ethical standards. His vision drives DRK's commitment to expanding access to innovative therapies, particularly for underserved populations across LMICs in Europe, the Middle East, Asia, Africa, and the Americas.

Head Of Business Development
Azka Wase is the Head of Business Development at DRK Research Solutions SA, responsible for driving strategic partnerships and expanding the company's global client base across the pharmaceutical and biopharmaceutical sectors. With a strong foundation in life sciences and commercial strategy, Azka leads efforts to connect sponsors, research institutions, and healthcare partners with DRK's end-to-end CRO and CDMO capabilities. Her work spans DRK's operational regions, including Europe, the Middle East, Asia, Africa, and the Americas. Azka is committed to building meaningful, long-term collaborations that accelerate drug development timelines and ultimately improve patient access to innovative treatments worldwide.

Chief Scientific Officer
Vipan Dhall, Ph.D., serves as Chief Scientific Officer at DRK Research Solutions SA, leading the company's scientific strategy and innovation agenda. With advanced expertise in pharmaceutical sciences, Dr. Dhall oversees the scientific direction of clinical development programs and CDMO services, including generics and hybrid product development for regulated markets. He plays a central role in ensuring that DRK's research methodologies meet the highest standards of scientific rigor and regulatory compliance. Dr. Dhall is passionate about leveraging cutting-edge science and technology to bring therapies to patients faster, consistent with DRK's core value of innovation with purpose and its mission to enhance global healthcare access.

Clinical Trials Implementation Specialist
Dr. Isabel Potani, PhD, is a Clinical Trials Implementation Specialist at DRK Research Solutions SA, bringing specialized expertise in the design, coordination, and execution of clinical trials across diverse international settings. With a particular focus on multi-regional clinical trials, Dr. Potani ensures rigorous implementation standards are maintained from site initiation through study completion. Her background and dedication to patient-centric research make her especially effective in trials targeting underserved and LMIC populations. Dr. Potani collaborates closely with global sponsors, site investigators, and regulatory bodies to deliver high-quality clinical data while prioritizing participant safety and study integrity throughout every phase of the trial process.

Chief Medical Officer
Dr. Zenaida Reynoso-Mojares serves as Chief Medical Officer at DRK Research Solutions SA, providing senior medical leadership across the company's clinical development portfolio. With extensive experience in clinical medicine and pharmaceutical research, she oversees medical strategy, patient safety, and the medical integrity of DRK's clinical trial programs from Phase II through Phase IV. Dr. Reynoso-Mojares ensures that all clinical activities adhere to the highest GxP, ethical, and regulatory standards across DRK's global operational regions, including Europe, the Middle East, Asia, Africa, and the Americas. Her patient-centric philosophy aligns with DRK's core mission of improving healthcare access for underserved populations worldwide.

Regional Head – USA & Africa
Dr. Onesmo Mpanju is the Regional Head for USA & Africa at DRK Research Solutions SA, leading the company's strategic operations and business development activities across two of its most impactful regions. With a strong background in pharmaceutical research and regional healthcare systems, Dr. Mpanju manages DRK's presence at its Aldie, Virginia office while fostering key relationships with sponsors, research institutions, and healthcare partners across the African continent. His expertise in navigating diverse regulatory environments and his dedication to expanding clinical research capabilities in underserved African markets directly support DRK's mission to enhance global healthcare access, particularly for low- and middle-income country populations.

Senior Strategic Advisor
Dr. Zafar Mirza brings distinguished expertise to DRK Research Solutions SA as Senior Strategic Advisor, providing high-level guidance on global health policy, regulatory strategy, and pharmaceutical development. With a career spanning international health organizations and pharmaceutical research, Dr. Mirza offers invaluable insight that helps shape DRK's long-term strategic direction. His advisory role supports the company's mission to bridge global healthcare gaps and improve access to modern treatments, particularly in underserved regions. Dr. Mirza's deep knowledge of global regulatory landscapes and his commitment to equitable healthcare access make him a cornerstone of DRK's leadership team and an essential voice in the company's patient-centric philosophy.

Country Head UK
Dr. Nigel Whittle serves as Country Head UK for DRK Research Solutions SA, overseeing all operations and business activities from the company's Cambridge, United Kingdom office. With extensive experience in the UK pharmaceutical and clinical research landscape, Dr. Whittle manages local stakeholder relationships, regulatory engagements, and business development across the United Kingdom and broader European markets. He ensures that DRK's UK operations maintain the highest standards of compliance and service delivery consistent with the company's global reputation. Dr. Whittle's localized expertise combined with DRK's worldwide capabilities enables seamless delivery of CRO and CDMO services to pharmaceutical and biopharmaceutical clients across Europe.

Regional Head - Southeast Asia
Muhammad Mazree is the Regional Head for Southeast Asia at DRK Research Solutions SA, directing the company's operations and growth strategy from its Shah Alam, Selangor, Malaysia office. With deep knowledge of the Southeast Asian pharmaceutical market, regulatory environment, and clinical research ecosystem, Muhammad manages key regional partnerships and oversees business development activities across this dynamic and rapidly growing market. He ensures that DRK's global CRO and CDMO capabilities are effectively delivered to local pharmaceutical and biopharmaceutical clients while maintaining the company's exacting standards of quality and compliance. His regional leadership is critical to DRK's mission of expanding healthcare access across Asia.

Clinical Data Manager
Krishnaveni Thanappan is a Clinical Data Manager at DRK Research Solutions SA, specializing in the collection, management, and quality assurance of clinical trial data across DRK's global studies. With expertise in data management systems and regulatory-compliant processes, Krishnaveni ensures the integrity, accuracy, and completeness of clinical data from trial initiation through database lock. Her meticulous approach supports DRK's commitment to delivering high-quality evidence that meets the rigorous standards of global regulatory agencies. Krishnaveni works collaboratively with clinical operations, biostatistics, and sponsor teams to maintain seamless data flows, contributing directly to the success of multi-regional clinical trials and the advancement of innovative pharmaceutical therapies.

Lead PMD & OD
Maha Fareed serves as Lead Project Management & Organizational Development (PMD & OD) at DRK Research Solutions SA, driving the effective planning, execution, and delivery of the company's complex pharmaceutical and clinical research projects. With a strong background in project management and organizational development, Maha ensures that DRK's cross-functional teams operate with efficiency, cohesion, and strategic alignment across its global offices. She plays a vital role in building internal capabilities and streamlining processes that support timely project delivery—one of DRK's key competitive advantages. Maha's commitment to fostering a diverse, inclusive, and high-performing workplace reflects DRK's core values and its vision for sustainable organizational growth.
Clinical trial monitoring services provide structured oversight of study sites, trial data, participant protection activities, and protocol compliance. Monitors review essential documents, informed-consent processes, source records, safety reporting, investigational product accountability, and site performance. The goal is to identify and resolve issues promptly, maintain reliable data, and ensure the trial is conducted in accordance with the protocol, applicable regulations, and good clinical practice expectations.
Speak with our clinical operations team about your study needs.
Coordinated clinical trial support across key international regions through operational hubs and strategic partner networks.
5 Global Regions
Service Coverage
24/7 Support
Availability
Since 2012
Experience
Discuss monitoring coverage aligned with your programme and sites.
Built around rigorous ethical and regulatory standards.
Multi-regional support through hubs and strategic alliances.
Focused on access, safety, and well-being.
Tell us about your trial phase, site footprint, and oversight priorities. Our team will help identify the right on-site, remote, or risk-based monitoring support.
For immediate assistance, feel free to give us a direct call at +41 76 797 25 67. You can also send us a quick email at info@drkresearch.com.
For immediate assistance, feel free to give us a direct call at +41 76 797 25 67. You can also send us a quick email at info@drkresearch.com.