Clinical Research Associate - Mechelen, België - SGS

SGS

Geverifieerd bedrijf

Mechelen, België

3 dagen geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

Company Description

As part of the world's leading testing, inspection and certification company, you share the benefits of our stability and growth; secure employment in a financially stable, Swiss-based company; a proud heritage that has been making the world a better, safer place for over 140 years; and a global, multicultural, and multinational organization.

Grow in a company that is the home of global knowledge and expertise; that operates in a wide range of countries, services and sectors; and that offers you endless opportunities to learn, grow and fulfill you potential

In the spirit of continued growth, we are currently looking for a Clinical research Associate (CRA).

As a clinical research associate you will be responsible for:

Participating in the trial set up activities
Preparing, translating, reviewing, finalizing, tracking and filing study documents
Conducting site initiation visits, monitoring visits (onsite and remote, in accordance with the monitoring plan) and closeout visits at assigned clinical site(s) according to applicable regulations, SGS procedures and study specific documents.
Writing site visit reports
Verifying the IMP management process at site (storage, return, accountability )
Managing trial sites
Ensuring compliance of the trial conduct with the protocol and the applicable guidelines, regulations and SGS procedures

You will work in close collaboration with other CRAs and the Study Team to ensure that quality and milestones are achieved within the budget and you will maintain regular contacts with the sponsor, project team and investigator.

Qualifications What do you need to be successful?**- You have obtained a university degree (equal to 4 years of college) in (para-) medical, pharmaceutical, sciences, life-sciences or bio-sciences. An equally recognized degree and/or relevant qualifications by experience may also be acceptable and will be evaluated on a case-by-case basis.

You can work in a selfdriven capacity, with a sense of urgency and limited need for oversight
You are fluent in both Dutch and English; knowledge of French is an asset
You are a strong communicator and have strong organisational skills
You work well independently as well as in a team
You are constantly dotting the i's and crossing the t's

- you have a good knowledge of ICH GCP and European Directives 200

You are accountable, helpful, dedicated and flexible
You are willing to travel, if necessary

- **Professional**: you bring quality, excellence, and ownership to everything you do
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Responsible and results-oriented: you have a sense of accountability for business results
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Committed: you bring your whole self to work with passion and focus
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Driven and eager: you are curious, flexible, and ambitious to learn from a global network
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Open to learning: from the range of different skills, backgrounds, and behaviors around you
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Capable of taking ownership and being independent:

Ambitious: you always challenge yourself to continuously improve and be the best you can be

Additional Information What we can offer you**:

A truly rewarding career, working at the highest level of international standards for quality, safety and integrity
The chance to share our growth and stability.
Continuous learning from the best experts in the industry
The chance to expand and enrich your career
Professional and personal growth
Experiences and opportunities across the global business

**Do you want to be part of this?