Freelancer profile translated to English.

Description

Clinical research specialist for over 10 years, I have acquired solid experience in several roles within the field.

I have worked for hospitals, associations, and CROs/Laboratories, as a research associate, coordinator, project manager, and as a Medical Science Liaison.

I have a perfect command of the medical device and drug environment and have worked on several international projects from phase II to IV.

I also have excellent command of the field of real-world data research and the use of AI for developing clinical studies.

Today, I focus on clinical project management and regulatory affairs positions. I also handle study start-ups (contract negotiations and essential document preparation).

I also accept some monitoring missions.

Industry field of expertise

Languages

English
Fluent
French
Native or bilingual
Spanish
Basic

Workplace preferences

Can work on-site

Toulouse (up to 50km), Paris (up to 100km), Bordeaux (up to km), Lyon (up to km), Marseille (up to km)

Savana
Medical Science Liaison
MEDICAL
September 2020 - March 2022 (1 year and 7 months)
Toulouse, France
MSL for French-speaking countries: France, Switzerland, and Belgium.
Big Data Clinical Research MR004 CNIL artificial intelligence
LL Clinical Consulting
Clinical Research Specialist
MEDICAL
April 2011 - Today (15 years and 2 months)
Toulouse, France
Clinical Project Manager:
9 years of experience in international clinical trial management.
My experience in cardiology began in 2011 and continues today depending on my assignments (over 5 years).
My experience in oncology began in 2016 and continues today (over 3 years).
My experience in Neurology began in 2011 and continues today depending on my assignments (over 2 years).

Study Start-up - Regulatory:
My experience in this area has been built since 2014, when I began clinical study start-up assignments: from phase II to IV, in medical devices and drugs, managing budgets and clinical contracts, and communications with competent authorities. I have led national and international clinical projects. I remain a specialist in the French market, although I have experience managing submissions in certain European countries (United Kingdom, Germany, Italy, Spain) and the USA.

Monitoring:
My monitoring experience began in 2013.
Project Management Regulatory Essential Documents Monitoring Coordination Team Management Autonomy Microsoft Office artificial intelligence GDPR Big Data
Abbott
Field Clinical Specialist
MEDICAL
March 2019 - September 2019 (7 months)
Paris, France
Internal Clinical Project Manager.
Clinical Product Specialist.
Clinical support to medical and paramedical teams (Cathlab).
Autonomy Rigor Availability project management Coordination Training

Check out Ludovic's experience

Be the first to recommend Ludovic

Help this freelancer shine by sharing your experience working together.

Agatha Frydrych

Backend Java Software Engineer

4.7

(3)

Baptiste Duhen

Fullstack developer

4.6

(4)

Amed Hamou

Senior Lead Developer

(2)

Audrey Champion

Web developer

4.3

(3)

Signup to reveal

Master 1 Physiology
Université Paul Sabatier Toulouse
2005
Master 2 in Neuroscience
Toulouse
2006
Master 2 en Recherche, spécialité Neurosciences. Gestion de projet Statistiques Pluridisciplinaire Cerveau Imagerie Animal

MOOC Project Management
Ecole centrale de Lille
2016
Medical Device Regulatory
ASPE Conseil
2016

Ludovic's certifications are only visible to Malt Community members

Other

Ludovic Lacassagne

Clinical Affairs Project Manager

About Ludovic

Experience

Recommendations

These freelancer profiles also match your criteria

Education

Certifications

Skill set

Categories