Rihab RAIS

Associate Partner

Paris, Île-de-France, France11 yrs 5 mos experience

Key Highlights

Over 14 years of experience in clinical trial management.
Expertise in managing international clinical studies across multiple therapeutic areas.
Certified in GCP, ensuring compliance with regulatory requirements.

Stackforce AI infers this person is a Clinical Research Professional with extensive experience in managing complex clinical trials.

Contact

Skills

Other Skills

EDCICH-GCPCTMS and CASCADEClinical MonitoringOncologyClinical Research trialsCROHIVCardiologyIntensive caresite managementBonnes pratiques cliniquesOncologie

About

Committed Clinical Trial Manager with a strong takeholder engagement skill and a result driven attitude. After more than 14 years of experience in international CRO and laboratories as a Lead Clinical Research Associate, Study Start up Specialist and Global Clinical Project Manager, I’m able to manage several international (phase I, II, III and IV) and observational clinical studies in various therapeutic areas such as: oncology, neurology, cardiology , haematology and rare diseases. Certified in GCP, I’m able to conduct studies in accordance with local regulatory requirements. Trained in project management, I’m determined to achieve company targets and clients’ goals.

Experience

11 yrs 5 mos

Total Experience

1 yr 6 mos

Average Tenure

4 mos

Current Experience

Pfizer

Associate Director-Senior Global Clinical Project Manager

Feb 2026 – Present · 4 mos

Servier

International Clinical Operations Lead

Apr 2024 – Feb 2026 · 1 yr 10 mos · Saclay, Île-de-France, France · Hybrid

Ergomed

2 roles

Senior Clinical Team Manager

Apr 2023 – Dec 2023 · 8 mos

Global Clinical Team Manager

Dec 2021 – Apr 2023 · 1 yr 4 mos

Cerc (cardiovascular european research center)

Global Clinical Project Manager

Aug 2021 – Dec 2021 · 4 mos · Greater Paris Metropolitan Region

Hays

Study Start up Specialist on behalf of ROCHE

Mar 2020 – Jul 2021 · 1 yr 4 mos

Abbvie

Senior Regional Clinical Research Associate

Apr 2019 – Mar 2020 · 11 mos · Rungis, Île-de-France, France

Ppd

Clinical Research Associate

May 2015 – Apr 2019 · 3 yrs 11 mos · Ivry sur Seine

Performs all aspects of the clinical monitoring and site management process in accordance with ICH GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation. Ensures that data will pass international quality assurance audits. Performes site management calls.Maintains collaborative relationships with investigational sites and client company personnel. Reviews study data from various sources.Contacts study sites to collect study documentation, resolves issues and requests outstanding information.