MARC

25/08/2026

Science is about discovery, and for 6 weeks, interns discovered their true potential. The closing ceremony gathered the brightest young researchers to celebrate their hard work. They stepped out of university labs and into real-world R&D, contributing to actual scientific progress. 🔬

23/08/2026

23/08/2026

Building the Future of Clinical Research Together

We are proud to share the successful collaboration between MARC and Sultan Bin Abdulaziz Humanitarian City (SBAHC) in delivering the “Clinical Trial Project Management” Workshop in Riyadh, Saudi Arabia, 19and 20 August

The workshop was led by our BD manager Walaaeldin Ahmed and brought together healthcare professionals and participants from diverse healthcare sectors across Saudi Arabia, creating a valuable platform for knowledge exchange, professional development, and strengthening clinical research capabilities. The workshop was accredited by the Saudi Commission for Health Specialties (SCFHS),

Our sincere appreciation goes to Sultan Bin Abdulaziz Humanitarian City (SBAHC) for the collaboration and support in making this initiative a success. We would also like to extend our appreciation to Baahith CRO for their kind support and contribution to this initiative.

Together, let’s continue to advance clinical research, empower healthcare professionals, and translate research into better outcomes for patients.

14/08/2026

Faster approvals are not only about speed.
They are about having the right system behind every step.
At MedAxis Clinical Research Center, we support clinical trial through structured regulatory coordination, organized study start-up workflows, and clear operational readiness.
Our approach helps clinical research teams achieve:
🔹 Efficient approval pathway
🔹 Streamlined study start-up
🔹 Coordinated site readiness
🔹 Faster operational alignment
🔹 Quality-driven ex*****on
🔹 AI-enabled workflow support
Because when the system is prepared, studies move with better clarity, stronger coordination, and greater confidence.

We make difficult studies Possible.
📩 For collaborations and technical briefings, contact us. [email protected]

11/08/2026

Join MARC, a leading research center that aims to advance science by conducting research in interdisciplinary disease areas. Our goal is to conduct high-priority and ethical basic, preclinical and clinical research, bridging the gap between science and community to improve health and quality of life.

Main Responsibilities:
-Prepare Clinical Study Reports (CSRs) and related study documents.
-Design and generate Electronic Case Report Forms (eCRFs).
-Perform data reconciliation activities in accordance with study-specific procedures.
-Prepare study protocols and associated documentation.
-Maintain study documentation, data tracking logs, and study records.
-Ensure compliance with study protocols, company Standard Operating Procedures (SOPs), and Good Clinical Practice (GCP) guidelines.

Requirements:
-Bachelor’s degree in pharmacy.
-Minimum of 1 year of experience in the bioequivalence field.
-Good organizational skills with strong attention to detail.
-Ability to work effectively within a team environment and meet study timelines.
-Good written and verbal communication skills.

Apply Now!
https://apply.workable.com/j/15CA0F157E

11/08/2026

At MEDAXIS Clinical Research Center, we transform complex clinical research into efficient, high-quality studies through scientific expertise, operational excellence, and a patient-centered approach.
Our therapeutic expertise includes:
🔹 Oncology
🔹 Neurology
🔹 Transdermal Patches
🔹 Subcutaneous Injections
From protocol ex*****on to participant care, our dedicated clinical teams and modern research facilities are built to deliver reliable data while maintaining the highest standards of quality, safety, and regulatory compliance.
Because challenging studies deserve experienced partners.
We make difficult studies Possible.

📩 For collaborations and technical briefings, contact us : [email protected]
https://www.medaxis-eg.com/

09/08/2026

Accelerating Clinical Trials Without Breaking the Budget. 💡

In today's fast-paced research environment, clinical trial sponsors face a dual challenge: getting to market sooner and managing burn rates. At MedAxis Clinical Research Center, we’ve re-imagined the process to deliver on both.
How? By combining efficiency with integrity:
✅Transparent Budgeting: Detailed, upfront cost analysis with zero hidden fees, enabling maximum savings and precise planning.
✅Accelerated Startup: Faster study initiation gets trials running sooner, drastically reducing timelines and controlling costs.
We are dedicated to making difficult studies possible through innovation and speed

Learn more about how we can accelerate your next trial: : https://lnkd.in/dnQMtUfw

📩For collaborations and technical briefings, contact us. [email protected] to arrange your technical briefing and learn more

02/08/2026

🚨 شراكة دولية جديدة تضع الشرق الأوسط وشمال أفريقيا على خريطة اعتماد البحوث الإكلينيكية

أعلنت المنظمة الدولية لاعتماد البحوث الإكلينيكية (IAOCR) تعيين مركز إم إي آر سي (M.A.R.C) للخدمات الطبية والأبحاث الإكلينيكية مركزًا إقليميًا معتمدًا لمنطقة الشرق الأوسط وشمال أفريقيا، في خطوة تستهدف رفع جودة واعتماد مواقع البحوث السريرية وفق أعلى المعايير العالمية.

وتمنح الشراكة المؤسسات والمراكز البحثية بالمنطقة فرصة الاستفادة من الدعم الفني والإرشاد وبرامج الاعتماد الدولية، بما يعزز الثقة في منظومة الأبحاث الإكلينيكية ويواكب المعايير العالمية.

وقال الدكتور جورج ماهر، المدير العام لمركز M.A.R.C، إن هذه الشراكة تمثل محطة مهمة لدعم الباحثين والمؤسسات، وترسيخ ممارسات بحثية عالية الجودة تسهم في تحسين مخرجات الرعاية الصحية.

فيما أكدت جاكلين جونسون نورث، الرئيس التنفيذي للمنظمة الدولية لاعتماد البحوث الإكلينيكية، أن التعاون مع مركز M.A.R.C سيوسع نطاق تطبيق معايير الجودة الدولية في المنطقة، ويدعم بناء منظومة أكثر قوة واستدامة للبحوث السريرية.

وكشف الدكتور ولاء الدين أحمد، مستشار الشراكات الإقليمية بالمركز، عن هدف طموح يتمثل في اعتماد 100 موقع للأبحاث السريرية في منطقة الشرق الأوسط وشمال أفريقيا بحلول عام 2030، بما يفتح المجال أمام آلاف المرضى للوصول إلى علاجات مبتكرة، خاصة في مجالات الأورام، والأمراض النادرة، والمناعة، والغدد الصماء.

#الصحة

02/08/2026

https://economygates.com/%D8%B4%D8%B1%D8%A7%D9%83%D8%A9-%D8%A7%D8%B3%D8%AA%D8%B1%D8%A7%D8%AA%D9%8A%D8%AC%D9%8A%D8%A9-%D9%84%D8%AA%D8%B9%D8%B2%D9%8A%D8%B2-%D8%AC%D9%88%D8%AF%D8%A9-%D9%88%D8%A7%D8%B9%D8%AA%D9%85%D8%A7%D8%AF/

المنظمة الدولية لاعتماد البحوث الإكلينيكية (IAOCR) تعيّن مركز إم إي آر سي (M.A.R.C) للخدمات الطبية والأبحاث الإكلينيكية مركزاً إقليمياً معتمداً للمنطقة

30/07/2026

Effective clinical trial delivery starts with a site that is prepared, coordinated, and ex*****on focused.
At MedAxis Clinical Research Center, we support clinical studies through an integrated service model designed to improve coordination, readiness, and ex*****on across every critical study stage.
Our services are built around:
🔹Feasibility alignment.
🔹Study start-up support.
🔹Participant coordination and follow-up.
🔹Dedicated clinical trial site model.
🔹Experienced research-focused team.
🔹Quality-driven ex*****on.
🔹AI-enabled workflow support.
By combining focused operations, experienced teams, and structured study support, MedAxis helps clinical research teams move from planning to ex*****on with confidence.

We make difficult studies Possible.
📩 For collaborations and technical briefings, contact us. https://www.medaxis-eg.com/