Your Clinical Research Ambassador in MENA and Türkiye

Bringing Hope to patients

Full Service CRO delivering faster patient recruitment and life-changing therapies across MENA & Türkiye

Explore our capabilities

Our Experience in Numbers

Experience that speaks for itself.

100+

Clinical trials

20,000+

Patients

282

Trial sites

70+

Indications

Quality & Why Phoenix Clinical Research

Since 2012, personally committed to every clinical trial and every patient

Quality, regional experience and responsive support for your clinical research journey.

Quality
ISO

Accredited full-service CRO

Phoenix Clinical Research is an ISO-accredited full-service CRO in the MENA region, with focus on the quality of its deliverables.

Cybersecurity
950 / 1000

CyberVadis assessment score

Mature

Phoenix Clinical Research’s reported CyberVadis cybersecurity assessment result.

Expertise

Regional knowledge.
International experience.

International and regional expertise, combined with a flexible structure and a responsive approach to collaboration.

Trial Rescue

Phoenix Clinical Research, rising to the rescue of struggling clinical trials.

Expertise when clinical trials need it most.

Our Services

Expertise for every stage of your project.

Explore our services and capabilities, then tell us how we can support your project.

Clinical Operations

From site selection to study delivery, connect experienced teams, regulatory understanding and hands-on oversight across Phase I–IV trials.

Explore capabilities (4)
Clinical Trial Management (Phase I-IV)
  • Experienced Project Managers
  • Management of Plans, Budget, Resources, and Allocation
  • Risk Management, Reporting, Analysis, and CAPA Implementation
Site Feasibility
  • Thorough site feasibility assessments to identify suitable sites and patient populations
  • Strong network of investigators across the MENA Region
  • Rapid feasibility turnaround and high site engagement
Remote and On-site Monitoring
  • Experienced Study Monitors and CRAs Specialized by Therapeutic Area
  • Strong Relationships with Key Stakeholders
  • Well-Trained Staff with Continuous Learning Programs
Regulatory Submissions
  • Continuously Updated Regulatory SOPs
  • Comprehensive File Preparation and Submission
  • Support for Ad-Hoc Activities and Safety Management
  • Full Awareness of Local Regulatory Requirements
Explore service

Medical Writing & Biostatistics

Turn scientific information into clear communication and robust analysis, with connected medical writing and biostatistics expertise.

Explore capabilities (2)
Medical Writing
  • Coverage of Advisory Boards and Scientific Workshops
  • Consensus Panels
  • Clinical Writing
  • Writing & Submission of Articles for Publication
  • Writing & Submission of Congress Abstracts and Posters
  • Preparation of Educational Materials
  • Web Content
  • Oral Presentations
Biostatistics
  • Sample Size Calculation
  • Preparation of Statistical Analysis Plans
  • Statistical Analysis
  • Generation of Tables, Listings, and Figures (TLFs)
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Vigilance

Support safety oversight throughout the product lifecycle with vigilance systems, reporting and locally informed expertise.

Explore capabilities (7)

Vigilance (Pharmacovigilance, Materiovigilance, Cosmetovigilance, Nutrivigilance)

  • Pre & Post Marketing
  • Preparation and Submission of PSURs, PBRERs, and Addendum to Clinical Overview (ACOs)
  • PV System and QMS Set-up and Maintenance
  • QPPV and Deputy QPPV Assignment
  • Literature Screening
  • AEs / SAEs Management
  • ICSR Reporting & Follow-Up
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Clinical Research Coordination

Connect sponsors, investigators and site teams to support day-to-day trial delivery, quality and patient care.

Explore capabilities (4)
  • Patient Screening and Enrolment
  • Manage day-to-day trial activities, ensure data quality and accuracy, maintain regulatory compliance
  • Close support to patient safety and care
  • Serve as the communication bridge between sponsors, investigators, and site teams, reducing gaps and preventing delays
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Decentralized Clinical Trials

Bring research closer to patients through hybrid and fully decentralized study models, remote visits and connected data.

Explore capabilities (5)
  • Implementation of Hybrid and Fully Decentralized Study Models
  • Remote Patient Recruitment, e-Consent, and Telemedicine Visits
  • Real-Time Data Capture and Centralized Monitoring
  • Patient-Centric Approach to Improve Retention and Engagement
  • Compliance with Global and Local Regulatory Requirements
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Functional Service Provider

Extend your team with experienced professionals, with full-time or part-time support aligned to your program.

Explore capabilities (3)
  • Staffing on a Program Basis for Big Pharma companies
  • Full-Time and Part-Time Support
  • Experienced Professionals with Excellent Integration
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Market Access

Navigate the path to market with regulatory affairs, submission, pricing and reimbursement support.

Explore capabilities (5)
  • Regulatory Affairs Support for Pre-Marketing, Marketing Authorization, and Post-Marketing Stages
  • Development of Market Access Strategies and Local Launch Support
  • Complete Dossier Preparation and Submission
  • Regulatory Submissions, Pricing, and Reimbursement Management
  • Regulatory Consultancy & Ad-Hoc Regulatory Activities and Safety Management
Explore service

Patient Support Programs

Support patients through education, adherence management, outcome tracking and reimbursement assistance.

Explore capabilities (4)
  • Outcome Progress Tracking of the Patient
  • Patient Education
  • Adherence & Compliance Management
  • Reimbursement Support
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Health Economics

Build the economic evidence to inform value discussions, budget planning and healthcare decisions.

Explore capabilities (3)
  • Pharmacoeconomics studies
  • Budget Impact Analysis
  • Cost-Effectiveness and Outcomes Studies
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Trainings

Develop practical capabilities through tailored programs for healthcare professionals, pharmaceutical teams and related stakeholders.

Explore capabilities (3)
  • Tailored Programs for HCPs, Pharma, and Related Stakeholders
  • GxP Workshops and Compliance Training
  • Functional trainings in Medical Writing, Biostatistics, Regulatory Affairs, Pharmacovigilance and Market access
Explore service

Vendor Support

Connect your study with the specialist partners, infrastructure and oversight it needs.

Explore capabilities (5)
  • Data Management Solutions
  • Central & Local Laboratories Support
  • Imaging and Specialty Vendors
  • Clinical Supply and IP Logistics Support
  • Vendor Qualification and Oversight
Explore service

Our Locations

Regional presence.
Local understanding.

Connecting clinical research across MENA and Türkiye.

Lebanon

Office

Beirut · HeadquartersBerytech Technology & Health, 4th Floor, Damascus Road.

Egypt

Office

CairoE13 Kapitalize Offices, 3rd Floor, Tower 12, Bavaria Town, Ring Road.

United Arab Emirates

Office

DubaiDubai Science Park, South Tower, 13th Floor (D/Quarters).

Saudi Arabia

2 Offices

JeddahNahdat Al Fikr, AR Rawdah District.

Riyadh6252 Turki Al Awal Road.

Tunisia

Office

Centre Urbain Nord, Le Cercle des bureaux, Boulevard de la Terre.

Türkiye

Office

AnkaraKızılırmak Mah. Dumlupınar Bul. No:9A
İç Kapı No: 158

Additional country coverage

  • AlgeriaCoverage
  • BahrainCoverage
  • IraqCoverage
  • JordanCoverage
  • KuwaitCoverage
  • LibyaCoverage
  • MoroccoCoverage
  • OmanCoverage
  • QatarCoverage

What Our Collaborators Say

Experience, in their words.

Perspectives from professionals who have worked with Phoenix Clinical Research.

Arafat Tfayli, MD

Department of Internal Medicine, Division of Hematology / Oncology, American University of Beirut Medical Center, Beirut, Lebanon

Over the ensuing 12 months, the Phoenix Clinical Research team proved to be of great help. A very reliable group of individuals, well familiar with the whole process, helped me and my team go through all these steps with little difficulty.

Read full testimonial

One year ago, I received a large research grant for a multi-center investigator-initiated research trial. While that was very exciting for me, I felt a big burden had been laid on my shoulders; how to write a detailed proposal, finalize the budget, get contracts, IRB approval, coordination with other centers, etc.

At that point, my research team got in touch with Phoenix Clinical Research, a well-respected CRO.

Over the ensuing 12 months, the Phoenix Clinical Research team proved to be of great help. A very reliable group of individuals, well familiar with the whole process, helped me and my team go through all these steps with little difficulty. They put up with hundreds of meetings and emails and phone calls, while maintaining a professional attitude and a very receptive accommodating behavior.

I am sure, my journey through that process would have been much harder without this wonderful team.

Hiba Baroudi, PharmD

Senior Medical Manager Diabetes Levant, Medical Capability Manager Near East “AstraZeneca”

I worked several projects with Phoenix Clinical Research and I highly recommend them for their professionalism, quality services and punctuality.

Dr. Samir Tawil

Head of Consulting Department, Konoz Retaj

A time-based Project has a specific deadline, The Phoenix Clinical Research Team proved to be very professional, accurate, helpful, familiar with all tasks needed, and creative, while keeping quality and productivity in tandem with an exceptionally positive attitude and a wonderful team.

Let’s Move Research Forward

Your next milestone starts with a conversation.

Tell us about your project and where you want to go next.

LET’S DISCUSS YOUR PROJECT

How can we support you?

Tell us about your project and the expertise you need.

Please do not include patient-identifiable information or confidential study details.