Sandrine V.-Independent Clinical Research Professional
Check rate
Experience
Independent Clinical Research Professional
ClinARC
- Provided consultancy and operational leadership to global pharma and CROs.
- Roche (2001–Present): EU CTR Business Process Owner (active); Veeva SSU module part of the global implementation SME team (active); delivering ICH/GCP (R2&R3) training (active); Global SIP Adoption Lead (inactive); People Leader (inactive); Regional Study Manager (inactive); Country Study Manager (inactive); Therapeutic Area Lead for non-oncology trials in Belgium (non-active)
- AMS (2022–Present): CRA for Parkinson disease clinical trial
- Novellas (2017–2019) and ClinOpsHub (2025–Present): ICH GCP trainer for sponsors and investigators
- Brunel (2012–2015): CRA training and onboarding for junior CRAs
- AbbVie, Biogen, Sanofi, Novo Nordisk and Ferring (2001–2013): Clinical Operations roles
- Clinical Trial Regulation (CTR): Successfully co-led the transition of 125+ clinical trials, consistently delivered ahead of regulatory deadlines
- Process excellence: Designed and implemented a robust CTR submission and post-approval framework, ensuring compliance and operational efficiency across both in-house and outsourced study teams
- Site Investigator Portal (SIP): Directed the onboarding of 1,000+ investigators worldwide, driving global adoption of SIP functionalities and strengthening affiliate engagement
- Training and development: Delivered ICH/GCP training programs to sponsors and investigators, achieving consistently high participant satisfaction and feedback scores
- Leadership agility: Recognized for the ability to rapidly integrate into new roles and environments, leveraging extensive experience to provide immediate operational value
Clinical Research Associate
Omnicare Clinical Research
- Managed site monitoring, submissions and investigator feasibility
- Built early expertise in clinical trial operations and GCP compliance
Material Management Officer
Hoechst Marion Roussel
- Served as intermediary between Hoechst AG and Belgian drug purchasers and oversaw company fleet (140 cars) and procurement operations
Industry experience
See where this freelancer has spent most of their professional time.
Experienced in Pharmaceutical, Biotechnology, and Healthcare.
Business area experience
See which departments and functions this freelancer has contributed to most.
Experienced in Quality Assurance, Research and Development, Project Management, Logistics, and Procurement.
Summary
Senior Clinical Operations Leader with 25+ years of experience driving regional and country trials across multiple therapeutic areas. Proven track record implementing EU CTR processes, building and managing high-performing teams of 90+ professionals and leading SIP adoption worldwide. Combining strategic leadership and operational expertise with a psychology background to deliver sustainable success in complex, matrixed environments. I thrive on complex challenges and bring passion, resilience, and strategic leadership to deliver sustainable success in matrixed, multinational environments.
Skills
- Global, Regional & Local Clinical Operations Leadership
- Ema Ctr Sme
- Ich/Gcp (R3) Certified Trainer & Audit Compliance
- Systems Knowledge: Siebel Ctms, Veeva Ctms, Rave, Clincase, Sip, Google Suite, Veeva Ssu Module (Part Of The Global Implementation Sme)
Languages
Education
KU Leuven
Master in Fundamental & Industrial Psychology · Fundamental & Industrial Psychology · Leuven, Belgium
KU Leuven
Candidatures in Psychology · Psychology · Leuven, Belgium
OLV ter Engelen Lyceum
Mathematics/Economics · Kortrijk, Belgium
Certifications & licenses
ICH/GCP (R3) Certified Trainer & Audit Compliance
Statistics
Experience
Global experience
Expertise
Qualifications
Profile
Frequently asked questions
Have questions? Find more information here.
Sandrine is based in Asse, Belgium.
Sandrine speaks the following languages: French (Native), Dutch (Native), English (Advanced), German (Elementary).
Sandrine has at least 31 years of experience. During this time, Sandrine has worked in at least 3 different roles and for 3 different companies. The average length of individual experience is 10 years and 3 months. Note that Sandrine may not have shared all experience and actually has more experience.
Based on recent experience, Sandrine would be well-suited for roles such as: Independent Clinical Research Professional, Clinical Research Associate, Material Management Officer.
Sandrine's most recent position is Independent Clinical Research Professional at ClinARC.
In recent years, Sandrine has worked for ClinARC.
Sandrine is most experienced in industries like Pharmaceutical, Biotechnology, and Healthcare.
Sandrine is most experienced in business areas like Quality Assurance, Research and Development, and Project Management. Sandrine also has some experience in Logistics and Procurement.
Sandrine has recently worked in industries like Biotechnology, Healthcare, and Pharmaceutical.
Sandrine has recently worked in business areas like Project Management, Quality Assurance, and Research and Development.
Sandrine holds a Master in Fundamental & Industrial Psychology from KU Leuven.
Sandrine has 1 certificate: ICH/GCP (R3) Certified Trainer & Audit Compliance.
The availability of Sandrine needs to be confirmed.
Daily rate distribution
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Average rates for similar positions
Rates are based on recent contracts and do not include FRATCH margin.
The average daily rate is the mean of all daily rates from recent contracts of comparable freelancers on our platform.
The median daily rate is the middle value of all daily rates — half of comparable freelancers charge less, half charge more. Unlike the average, it is barely affected by outliers.
Calculated based on our freelancers’ daily rates as of 27 Sep 2026. Actual rates may vary depending on seniority level, experience, skill specialization, project complexity, and engagement length.
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