Bram Verdonckt Email & Phone Number | I am currently working as a Clinical Study Lead in a global Phase 2 trial. I am always interested in Project management opportunities in Clinical Research. I am a Freelance Clinical Research Associate / Project Manager specialized in supporting clinical trials in different areas for phase I up to IV clinical trials according to ICH-GCP standards. I am highly experienced with the complete trial cycle, from feasibility through submissions initiation, monitoring and close-out. 20 years of experience in clinical trials in both pharmaceutical and medical device industries: - 5 years of project management in global clinical trials. - 5 years of monitoring phase II-III trials in oncolology trials. - International CRA monitoring in Belgium, the Netherlands, Germany and Croatia for a biotech company (Orthopaedics). - Coordinating CRA responsible for CRA training, presentations and organization of Investigator Meetings and Project Management tasks including CRF / Protocol design, CSR review, etc. - Thorough experience in managing the imaging logistics (collection, validation, storage and analysis of MRI, CT, Rx, etc.) during clinical trials. - Experience with internal company audits, FDA inspections and EMEA inspections. - Several trials in various therapeutic areas including Oncology, Nephrology (Hemodialysis), Renal and LiverTransplant, Rheumatology, Diabetes, gastroenterology , Dermatology, Neurology and Phase 1 first in human . Specialismen: - Dermatology (3+ years) - Oncology (5+ years) - Orthopaedics (2,5 years) - Rheumatology (10+ years) - Renal and LiverTransplant (1,5 years) - Nephrology (2 years) - Phase 1 (first in human) - Start-up expert: Feasibilities, Pre-study visits, Submissions & SIVs for several projects.

Bram Verdonckt

I am currently working as a Clinical Study Lead in a global Phase 2 trial. I am always interested i...
Leuven Flemish, Leuven Flemish, Belgium

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Bram Verdonckt’s Email bram.verdonckt@glpg.com

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Bram Verdonckt’s Location Leuven Flemish, Leuven Flemish, Belgium

Bram Verdonckt’s Current Industry Argenx Clinreach

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Work Experience

Argenx

Clinical Trial Manager

2024-08-01 00:00:00 - Present

Clinreach

Freelance Clinical Study Lead / Project Manager

2010-05-01 00:00:00 - Present

Alfasigma

Clinical Study Lead

2024-04-01 00:00:00 - 2024-07-01 00:00:00

Galapagos

Clinical study Lead

2019-04-01 00:00:00 - 2024-03-01 00:00:00

Celyad

Clinical Trial Manager

2018-10-01 00:00:00 - 2019-04-01 00:00:00

Dedevan

Clinical Research Associate (outsourced Novartis)

2009-01-01 00:00:00 - 2010-05-01 00:00:00

Tigenix

Clinical Research Associate

2006-01-01 00:00:00 - 2008-12-01 00:00:00

Medisearchsgs

Clinical Research Associate (outsourced)

2004-01-01 00:00:00 - 2006-02-01 00:00:00

Medisearch

Clinical Trial Assistant (outsourced)

2003-05-01 00:00:00 - 2004-01-01 00:00:00

Skills

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Languages

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FAQ About Bram Verdonckt

Bram Verdonckt is located at
Leuven Flemish, Leuven Flemish, Belgium

Bram Verdonckt is a I am currently working as a Clinical Study Lead in a global Phase 2 trial. I am always interested in Project management opportunities in Clinical Research. I am a Freelance Clinical Research Associate / Project Manager specialized in supporting clinical trials in different areas for phase I up to IV clinical trials according to ICH-GCP standards. I am highly experienced with the complete trial cycle, from feasibility through submissions initiation, monitoring and close-out. 20 years of experience in clinical trials in both pharmaceutical and medical device industries: - 5 years of project management in global clinical trials. - 5 years of monitoring phase II-III trials in oncolology trials. - International CRA monitoring in Belgium, the Netherlands, Germany and Croatia for a biotech company (Orthopaedics). - Coordinating CRA responsible for CRA training, presentations and organization of Investigator Meetings and Project Management tasks including CRF / Protocol design, CSR review, etc. - Thorough experience in managing the imaging logistics (collection, validation, storage and analysis of MRI, CT, Rx, etc.) during clinical trials. - Experience with internal company audits, FDA inspections and EMEA inspections. - Several trials in various therapeutic areas including Oncology, Nephrology (Hemodialysis), Renal and LiverTransplant, Rheumatology, Diabetes, gastroenterology , Dermatology, Neurology and Phase 1 first in human . Specialismen: - Dermatology (3+ years) - Oncology (5+ years) - Orthopaedics (2,5 years) - Rheumatology (10+ years) - Renal and LiverTransplant (1,5 years) - Nephrology (2 years) - Phase 1 (first in human) - Start-up expert: Feasibilities, Pre-study visits, Submissions & SIVs for several projects.

Bram Verdonckt currently works in the Argenx | Clinreach |

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Bram Verdonckt has prior
experience in the following industries:
Alfasigma | Galapagos | Celyad | Dedevan | Tigenix | Medisearchsgs | Medisearch

Bram Verdonckt has the following professional experience:
Argenx | Clinreach | Alfasigma | Galapagos | Celyad | Dedevan | Tigenix | Medisearchsgs | Medisearch