Clinical research
Monitoring, GCP/ICH, CRO coordination, multicentre study follow-up, data quality and query management.
Clinical research · Medical affairs · MSL
Miyah SaisTurning scientific rigor into a force for action.
Medical Doctor · Medical Affairs · Clinical Research
More than twenty years of experience spanning field medical work, clinical operations, Medical Excellence and scientific project leadership across pharmaceutical and medical-device environments.
Open to new scientific, medical or clinical projects
- years across healthcare
- 20+
- years at Sanofi · 2002—2016
- 14
- countries coordinated on a MedTech assignment
- 04
01 · Executive profile
A dual medical and operational perspective.
A medical doctor by training, Miyah Sais has built her career around clinical research, medical affairs and healthcare product development across both the pharmaceutical and medical-device industries.
She held field and scientific leadership roles at Sanofi and Merck, then structured Medical Affairs for a CE-marked Class III medical device, producing an Evidence Book, literature review and competitive benchmark while coordinating partners across four countries.
She works comfortably in scientific and regulated environments including GCP/ICH, MDR 2017/745 and pharmacovigilance, interacting with medical teams, MSLs, sales, CROs, healthcare professionals and cross-functional stakeholders.
Connect scientific evidence, coordination and operational execution.
02 · Expertise
Capabilities grounded in clinical and medical practice.
Six areas of practice directly reflected in the updated professional record.
Medical affairs & MSL
Field medical engagement, healthcare professional training, MSL team leadership and KOL / Thought Leader relationships.
Product launch & management
Launch plans, patient support programmes (PSP) and coordination across medical, marketing and market access functions.
Regulatory compliance
Pharmacovigilance, MDR 2017/745, medical documentation, medical ethics and good clinical practice.
Project management
Action plans, KPI dashboards, internal and external stakeholder coordination, including multi-country projects.
Medical Excellence & cross-functional leadership
Multidisciplinary team management, advisory boards, governance of medical activities and MSL tracking tools.
03 · Contribution
Structure, coordinate, secure.
A contribution at the intersection of scientific evidence, regulatory requirements and operational realities.
Structure Medical Affairs
Build the scientific foundations of a medical function through Evidence Books, literature review, competitive benchmarking, documentation and action priorities.
Lead clinical operations
Coordinate studies, CROs and partners, oversee data quality and anchor activities in GCP/ICH and MDR 2017/745 requirements.
Orchestrate products, teams and stakeholders
Support launches, PSPs, MSL teams and cross-functional projects through action plans, KPIs and multi-function coordination.
04 · Target assignments
Applying senior experience to scientific, medical or clinical projects.
Responsibilities consistent with the experience and capabilities documented in the updated résumé.
Medical Affairs
Structuring or strengthening a medical function, scientific strategy, documentation and cross-functional coordination.
Clinical Research / Operations
Monitoring, study coordination, CRO oversight, data quality and multicentre study follow-up.
MSL & Medical Excellence
MSL team leadership, KOL engagement, healthcare professional training and improvement of medical practices.
Product Launch & PSP
Healthcare product launches, patient support programmes and coordination across medical, marketing and market access functions.
Medical Device
Medical affairs and clinical activities for medical devices in an MDR 2017/745 environment.
Healthcare Project Management
Healthcare project leadership, action plans, KPI dashboards and multi-country stakeholder coordination.
05 · Career
From field medical work to scientific and clinical leadership.
Recent experience
Apr.—Jun. 2026
Medical Affairs Lead & Project Manager
Revitacare · Saint-Ouen-l’Aumône, France
- Structured the Medical Affairs function for a CE-marked Class III medical device: Evidence Book, literature review and competitive benchmarking.
- Developed an action plan and KPI dashboard, coordinating CROs and partners across four countries.
- Identified a clinical study aligned with MDR 2017/745 requirements with the objective of an indexed publication.
2024—2025
Project Manager
Yassir France · Paris, France
- Coordinated projects and interfaces between internal and external stakeholders in a multicultural environment.
- Implemented local marketing activities and analysed market data.
2020—2022
Healthcare Project Consultant
Axelys Santé · Algiers, Algeria
- Managed clinical studies and patient support programmes (PSP) in compliance with local regulations.
- Acted as interface with compliance bodies and monitored regulatory documentation.
2018—2022
Private Practice Physician
Private practice · Algiers, Algeria
- Managed medical practice independently, including scheduling, administration and patient relationships.
2017 · 6 months
Medical Manager Neurology NWA
Merck Group · Tunisia
- Led the launch of a new multiple-sclerosis product in coordination with medical, marketing and market access teams.
- Managed the dedicated patient support programme from design through field deployment.
Sanofi career · 2002—2016
2010—2016
Medical Excellence & Clinical Operations Lead
Coordinated clinical studies in diabetes, cardiology, oncology and infectious diseases. Oversaw CROs, advisory boards and pharmacovigilance, and managed a multidisciplinary team.
2007—2010
Medical Excellence Manager & Diabetes MSL Team Lead
Designed and deployed CoMet, a healthcare-professional management platform, across internal control, sales, marketing, medical and compliance teams. Implemented MSL tracking dashboards.
2005—2007
Infectious Diseases & Pain Product Physician / HSE Manager
Field medical activity in infectious diseases and pain. Validated promotional materials and ensured compliance with medical ethics and GCP/ICH.
2004—2005
Clinical Research Associate · Diabetes
Monitored diabetes clinical studies, contributed to data collection and quality, and ensured good clinical practice compliance.
2002—2004
Medical Representative · Infectious / Respiratory / Cardio-thrombosis
Provided medical and scientific information to healthcare professionals, developed a medical contact network and collected early pharmacovigilance information in the field.
06 · Scientific scope
A diverse scientific and operational field of experience.
Therapeutic areas & domains
- Diabetes
- Cardiology
- Oncology
- Infectious diseases
- Neurology
- Respiratory medicine
- Cardio-thrombosis
- Pain
- Aesthetic medicine
Stakeholders
- Healthcare professionals
- KOL / Thought Leaders
- CROs
- MSL teams
- Sales
- Marketing
- Market access
- Compliance
Frameworks & practices
- GCP / ICH
- MDR 2017/745
- Pharmacovigilance
- Query management
- Medical documentation
- PSP
07 · Education
Medical training complemented by digital marketing.
2022—2023
MBA in Digital Marketing
Devinci Executive Education · Paris
2016
Aesthetic Medicine Training
CIME · Paris
1992—2000
Medical Degree, General Medicine
Faculty of Medicine of Algiers
Languages
FrenchNative
ArabicNative
EnglishB2
08 · Contact
Discuss a scientific, medical or clinical project.
For assignments in clinical research, medical affairs, Medical Excellence, MSL, medical devices or healthcare project management.
France · International