DIEST : Assistant Study Director or Study Director

NAMSA SAS
BE - Flanders - Diest
December 29, 2024

About NAMSA :
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.
We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry's premier provider. We provide support for clients during every step of the product development lifecycle and beyond.
Come and work for an organization with the:
Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the
Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core
Values:
Act with integrity in everything we do.
Provide best-in-class customer experiences.
Develop superior talent and deliver expertise.
Respond with agility and provide timely results.
Embrace collaboration, diverse perspectives and ideas.
Your responsibilities:
We are looking for a motivated and dedicated Assistant Study Director/Study Director for a fixed term contract (6-8 months) to join our clinical biology lab and participate in all aspects of the pre-clinical studies:
Assists in the coordination of study conduct tasks from study initiation to study completion.
Supports in performing non-complex studies and may serve as the primary contact for the client.
Performs projects in compliance with applicable quality system regulations (i.e. ISO, GMP, GLP) and NAMSA SOPs.
Knows and understands the Animal Welfare Requirements and serves as Principal Investigator, when applicable.
May need to participate in study specific procedures.
Evaluates, analyzes and interprets data and presents in a clear, well-organized, scientifically sound report.
May need to ensure that study records for GLP studies are archived upon completion of the study.
Prepares protocol submissions for IACUC review and responds to committee comments/questions as necessary.
Participates in client discussions regarding study design when needed.
Establishes and ensures schedule, budget and quality commitments are met for the client.
Understands investigational products including high-level understanding of the Medical Device Development Process.
Other duties as assigned.
How to apply :
Please send CV and a cover letter in English.
Your qualifications:
To apply for the level of Study Director, a Master's degree/PhD with a minimum of one year of relevant laboratory experience is required.
To apply for the level of Assistant Study Director, a bachelor's degree with a minimum of one year of experience in the research environment is necessary.
Why you should join NAMSA :
A challenging and varied role at the affiliate in Belgium (Diest), part of NAMSA, a globally expanding company.
A highly professional team and a supportive working environment with the entrepreneurial can-do attitude of an SME.
An attractive remuneration package.
A permanent position may be offered to the selected candidate.
Job Types: Full-time, Fixed term contract
Contract length: 6 months
Pay: €2.080,00 - €2.700,00 per month
Benefits:
Company computer
Work Location: In person
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Read the full job description and apply online on the recuiter's web-site

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