Medical Advisor in Oncology - Brussels, België - Keyrus Life Science Belgium

Keyrus Life Science Belgium

Geverifieerd bedrijf

Brussels, België

1 week geleden

Geplaatst door:

Sophie Dubois

beBee Recruiter

Beschrijving

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.

Keyrus Life Science is looking for a
Medical Advisor in Oncology to join our consulting team for a client project based in
Brussels.

This is an office-based position (hybrid) so, if you join us, you will be expected to visit multiple sites for data collection and follow-up of clinical trail studies.

Your challenges will be:
-
Non-promotional scientific exchange with health care professionals to provide accurate, relevant and balanced data when needed.
-
Collect, collate and analyse insights from a variety of stakeholders to identify unmet needs and data gaps and share these insights with your cross functional team.
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Understand positioning of oncology products in the current landscape and provide medical strategic input to commercial, access, clinical and regulatory stakeholders accordingly.
-
Follow-up of investigator initiated
studies & local data-generating studies.

Connect with the
regional medical team to share the Belgian perspective, discuss on potential data gaps or local needs.

-
Review of market access dossiers for scientific accuracy.

Collaborating with local clinical trial operations and investigators to followup ongoing studies and identify opportunities to
implement new phase 2 and 3 studies in the country.

Profile

Musthave requirements:
Strong
oncology or genitourinary/urology expertise,
AND fluent in English + French or Dutch (with good command of the other national language).

-
OR trilingual (English, French & Dutch)
with experience as Medical Advisor or Medical Science Liaison (other diseases' expertise).
-
MD, PharmD or PhD Life Sciences.

Sound scientific and clinical judgment, understanding of clinical trial methods and interpretation of clinical data.
Strong
customer facing, listening, and probing skills.
Outstanding
communication skills with the ability to bring confident and engaging presentations.
Leadership skills: proactive
"can do" attitude and handson mentality; eager to continue to learn more.
Able to simultaneously handle multiple tasks and working under pressure.
Strong analytical skills, meticulous and eye for detail.
Excellent project and budget management skills.
Ability to function within a diverse team environment, across different departments and corporate cultures.
Compliance and quality mindset; compliant with business Integrity and Ethics standards.

Who we are

Keyrus Life Science is an international Consulting, Contract Research Organisation and Functional Services provider with 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.