Early Stage Development Scientist

☞ Keyrus

Visualizza: 170

Giorno di aggiornamento: 16-11-2025

Località: Waterloo Walloon Brabant

Categoria: R & D IT - Software

Industria: IT Services IT Consulting

Posizione: Associate

Tipo di lavoro: Contract

Loading ...

Contenuto del lavoro

What We Offer

Joining our consulting team in Belgium means giving your career a step forward. Thanks to the privileged partnership we have with our well-established clients, leaders in their domain, we offer our consultants unique projects to develop their skills, and put their professional experience in the pharma industry on the fast track.

As an expert on the client side, you can count on us to support you at each step of your project thanks to regular touch points with our Key Account Manager. We then also carefully choose with you what would be your next assignment that is matching your career goal whether it is in Consulting or in one of our Functional Services Platforms.

We invest considerable time and resources in training our staff (technical and non-technical courses) to continuously support you in your personal and professional growth. On top of this, you will receive a complete salary package including attractive extra-legal benefits (company car, petrol card, meal vouchers, group insurance, hospitalization…) based on your background and experience.

Job Description

Keyrus Life Science is looking for a Early Stage Development Scientist to join our consulting team for a client project based inBrussels. Where you will be cover your colleague who’s on maternity leave for 1 year.

As an Early Stage Development Scientist (ESDS) you will be responsible for the scientific elaboration and project management of early stage trials (also known as phase 1 trials) in Europe. This includes pro-actively organizing, coordinating and overseeing all critical aspects of set-up(including set-up of sites), conduct and reporting for clinical and developing scientific expertise with clinical sites.

Your challenges will be :

As a ESDS, you will be counted responsible from the first administration of the drug to first proof to consent.

Protocol drafts are provided by USA , you will adjust them following the Belgian legislation and do a feasability check.

You won’t have direct contact with our patients but do an observational monitoring of patients following the protocols. You will manage up to 4 or 5 trialsin diffrent stages at the same time.

Profile
  • Ideally you have a M.D, Vet MD or Phd and a MS in Life Sciences with at least 3 years’ experience in monitoring clinical studies.
  • Speaking and writing English and Dutch is a must. If you speak and write French this will be considered as a plus.
  • Due to covid you will work from home 4 days a week. Afterwards you are expected to come to the office 4 days a week.
  • Flexible in working hours: e.g when a monitoring starts at the Liège site at 8.30 am, the candidate has to be able to be present at the foreseen timeslot

Who We Are

Keyrus Life Science is an internationalConsulting, Contract Research Organisation and Functional Services providerwith a reputation for transparency and integrity, highly focused on being able to deliver with excellence. Our ‘human’ approach to service provision is what differentiates us from our competitors. Combined with our high caliber staff, this approach has allowed us to become a key player in clinical research.

At Keyrus Life Science we’re proud of our commitment to delivering services of the highest quality, not only skilfully, efficiently and reliably, but also with sincerity and genuine care for our clients’ projects, priorities and reputation. Thus we maintain and advance our vision and our standards, all the while ensuring that we serve your interests better.

From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical Writing & Medical Information, Real World evidence services.
Loading ...
Loading ...

Scadenza: 31-12-2025

Clicca per candidarti per un candidato gratuito

Applicare

Segnala lavoro
Loading ...

LAVORI SIMILI

Loading ...
Loading ...