Help us to build the world's best Biotechnology company focused on the great unmet Medical need of Anti-Microbial Resistance (AMR)?
Micreos Pharma is a highly innovative, fully fledged, biotechnology company focused on the targeted killing of bacterial pathogens (that harms human health) while protecting the rest of the Microbiome (that promotes good human health).
We are now looking for experienced, value-driven, customer-focused, medical professionals who can help us to bring our innovative technology through the clinical development progress and into the hands of healthcare providers and patients to impact the health and well-being of humanity.
Are you such a person? We would love to hear from you!
Your role at Micreos
You are responsible for the Design & Implementation of global clinical development plans for pharmaceutical products in the assigned therapeutic area as well as building the necessary Medical advocacy & consensus externally with top external experts (KOL’s) to support the development & approval of our medical technologies.
Therapeutic areas: Inflammatory Dermatological Diseases and Infections.
Main objectives of the role
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In collaboration with our Chief Medical Officer, external OL experts and internal Micreos senior leaders, design and execute development plans for the pursued indications in a therapeutic area. Ensure these are “stress tested” in the best possible way with experts in this field to maximise patient impact (including future labels) and minimise risk.
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Setup a network of KOL’s in the therapeutic area to discuss, check, validate the clinical development strategy to help make them advocates of Micreos Pharma and the technologies and mode of actions that we represent.
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Be the local therapeutic area expert within Micreos Pharma by staying up to date on literature, discussions with KOL’s, guidelines and SoC in clinical practice.
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Identify therapeutic development opportunities and to have the executional ability to deliver on these opportunities. Other tasks include:
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Support Clinical Operations in the execution of the clinical development plan
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Protocol writing
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Submission document generation/review
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Medical consensus alignment.
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Medical guideline understanding and the facilitation of external expert panels to update where this is the medically correct thing to do.
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Medical monitoring of assigned clinical trials
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Support clinical operations in setting clinical budgets and resource planning in therapeutic area
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Medical input to project management team
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Prepare with CHMO and RA submission documents and participate in the discussions with European (SAWP, COMP, CHMP), US-FDA and local authorities on strategy
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The role involves regular travel in the key (top-5) markets to ensure that the Micreos MD understands the market Standards of Care and is able to hold discussions with the right people to influence, evolve and update the medical guidelines to improve patient standards of care where appropriate.
More about you and your competences
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Medical degree
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Training in pharmaceutical development
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Good Clinical Practice
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Excellent cross functional collaboration skills.
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Experience of working in the pharmaceutical industry with a track record of delivering clinical and medical success.
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Minimum of 5 years’ experience in a clinical development organisation (pharmaceutical company and/or CRO) with tangible examples of success.
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Designed and executed clinical trials
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Interactions with regulatory authorities
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Therapeutic area experience is a must-have requirement.
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Great communication skills both verbal and written
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Able to connect with KOL’s and get them engaged
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Scientific thinking, data driven
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Next to English at least one more language
Our offer
Micreos offers a varied full time role within a young and enthusiastic team. The salary offered is in line with market conditions and you will be given the opportunity to make the fullest use of your talents. We offer you an ambitious and pleasant international working environment.
Is this the role you are looking for?
Our Micreos HR team is looking forward to receiving your CV and cover letter via recruitment@micreos.com. Any questions regarding the role can also be addressed to this email address.
Please only apply if you are eligible to work in the Netherlands.
Company profile Micreos Pharma:
Bacteria are all around us. Some of them are good and provide health benefits, but many can cause irritation or infection. It has become evident that our microbiome, comprising OF billions of beneficial bacteria, is necessary for our well being and should where possible be left intact. Traditional Antibiotics do not distinguish between good and bad bacteria and their overuse can lead to side effects and resistance which has the potential to cause significant issues for mankind. The emergence of the so called ‘antibiotic-resistant superbugs' is now of global concern.
Micreos develops the world's first targeted antibacterial products that are now being studied in a number of medical indications. The company is viewed as global leader spearheading this exciting new field. With Micreos endolysin technology, for the first time we can selectively kill only the unwanted bacteria - including antibiotic resistant strains - while leaving the beneficial bacteria intact. In addition, research shows that the use of endolysins does not induce resistance which potentially makes them suitable for longer term use in chronic conditions. This unlocks a completely new approach to dealing with the bacteria around us, enabling daily use while preserving the important biodiversity on our skin and in our gut.
This is an exciting time to join Micreos Pharma to improve standards of care for patients in select indications in dermatology and oncology.
Acquisitions following this vacancy are not appreciated.