Clinical Biomarker Principal Scientist job in Les Ulis, France

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First Name*

Last Name*

Email*

Phone Number*

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Are you an employer or a jobseeker?*

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First Name*

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Phone Number*

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Job type: Permanent

Discipline: Biological Sciences

Location: France

This vacancy has now expired. Please see similar roles below...

Proclinical are partnering with a biotech organisation who are recruiting for an individual to join their team. This role is on a permanent basis and is located in France. The opening position currently available is for a Clinical Biomarker Principal Scientist.

Responsibilities:

Oversee clinical execution and validation of biomarkers.
Assist the translational team in outlining the translational method to lead the clinical biomarker method using ground-breaking technologies.
Execute biomarker plans for clinical trials into clinical study documentation such as protocols, SoA, lab manual, etc.
You will select the most pertinent technical method to fulfil the biomarker targets which are FACS, tissue imaging, genomics, proteomics, etc.
Outline clinical biomarker methods and form biomarker plans for target engagement, pharmacodynamics, mechanism of action, and patient selection, collaborating with asset lead and therapeutic areas.
Expect the requirement for companion diagnostic and adapt biomarker method accordingly.
Other duties may be assigned.

Key Skills and Requirements:

Educated to an advanced degree level in a life science field, ideally within oncology or immuno-oncology.
Willing to travel for business needs up to 5% of the time.
A mixture of education and experience may be taken into consideration.
Demonstrable experience within drug development in a pharmaceutical or biotech organisation handling early phase clinical biomarkers.
Fluency in both French and English.
Communication skills both verbally and in writing.
Comprehension of the role of translational science and clinical biomarkers within drug development.
Familiarity within the suitable application of multiple scientific technologies into translational research methods.
Acquaintance with NGS and its implementation for companion diagnostics.
Prior involvement within companion diagnostic development and approval.
Able to work well within a fast-paced setting as well as in or leading a matrix team.
Capable of identifying, articulating, and accepting calculated risks to take notified decisions.
Know-how of all functional areas of drug development, which involves pharmacology, toxicology, clinical development, clinical operation, quality assurance, diagnostic development, etc.
Scientific insight and mechanistic comprehension of disease biology.
Able to think analytically as well as resolve issues.
Interpersonal abilities with the capacity to write scientifically.
Past involvement with clinical/lab practices.
Familiarity working with CROs.
A keen learner who wants to enhance their knowledge.

If you are having difficulty in applying or if you have any questions, please contact Sam Kennaugh at s.kennaugh@proclinical.com.

Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.

Proclinical Staffing is an equal opportunity employer.

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