General information
Publication date
20/10/2025 Category
OPERATIONS - CONSULTING
Job title
Clinical Trial Manager - Life Sciences - M/F/X
Contract
Permanent contract
Job description
About the role
Asa Clinical Operations Study Country Lead (COSCL) you will lead country-level operations for clinical studies ensuring strategic planning management and performance of assigned clinical trials.
You will be responsible for study timelines budgets and conduct at the Clinical Study Unit (CSU) level adhering to Standard Operating Procedures (SOPs) Quality Documents (QDs) and ICH/GCP guidelines.
Key responsibilities
- Develop and initiate local study country strategy and lead start-up activities
- Manage local study execution according to global and local study plans
- Optimize and manage study budget at country/cluster level
- Facilitate effective communication among local study parties to align goals
- Ensure data quality patient safety and compliance with study metrics
Business Industry
Life sciences
Profile
About you
- Bachelors degree in nursing biochemistry or related natural science
- Mandatory experience in clinical research and project management
- Strong skills in project management and problem-solving
- Proficiency in data analytics and use of digital tools
- Fluent in English and country languages (French & Dutch)
Job location
Europe Belgium Flanders
Location
Noordkustlaan 16B 1702 Dilbeek
Candidate criteria
Level of experience
3 to 5 years
Required Experience:
Manager
General information Publication date 20/10/2025 CategoryOPERATIONS - CONSULTINGJob titleClinical Trial Manager - Life Sciences - M/F/XContractPermanent contractJob descriptionAbout the roleAsa Cl...
General information
Publication date
20/10/2025 Category
OPERATIONS - CONSULTING
Job title
Clinical Trial Manager - Life Sciences - M/F/X
Contract
Permanent contract
Job description
About the role
Asa Clinical Operations Study Country Lead (COSCL) you will lead country-level operations for clinical studies ensuring strategic planning management and performance of assigned clinical trials.
You will be responsible for study timelines budgets and conduct at the Clinical Study Unit (CSU) level adhering to Standard Operating Procedures (SOPs) Quality Documents (QDs) and ICH/GCP guidelines.
Key responsibilities
- Develop and initiate local study country strategy and lead start-up activities
- Manage local study execution according to global and local study plans
- Optimize and manage study budget at country/cluster level
- Facilitate effective communication among local study parties to align goals
- Ensure data quality patient safety and compliance with study metrics
Business Industry
Life sciences
Profile
About you
- Bachelors degree in nursing biochemistry or related natural science
- Mandatory experience in clinical research and project management
- Strong skills in project management and problem-solving
- Proficiency in data analytics and use of digital tools
- Fluent in English and country languages (French & Dutch)
Job location
Europe Belgium Flanders
Location
Noordkustlaan 16B 1702 Dilbeek
Candidate criteria
Level of experience
3 to 5 years
Required Experience:
Manager
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