Clinical Scientist

MaaT Pharma is a clinical-stage biotechnology company and industry leader in microbiome therapies in oncology, leveraging our whole ecosystem restoration approach to develop biotherapies to treat serious diseases.

We are driven by our pioneering spirit, and are now the first microbiome-derived drug development company listed in continental Europe; we listed on EURONEXT Paris on November 8, 2021.

We have a humanistic approach to our entrepreneurial adventure. Every recruitment is an opportunity to consolidate our rich and diverse human capital, which will soon reach 50 people.

We are currently looking for a new:
**Clinical scientist - Regular - Full time**
- Position accessible to people with disabilities_

**_Your main responsibilities if you accept the role will be: _**

Directly attached to the Clinical Developments Director, you will work with the clinical team as part of the development activities of innovative therapies within MaaT Pharma, but not only. In this way, your mission will be:

- Develop scientific expertise on the clinical development of assigned products
- Contribute strategically to the clinical development plan, with knowledge of scientific and medical advances in the field
- Contribute to innovation and intellectual property generation in collaboration with company’s different teams
- Act as a clinical representative on study management teams to ensure the clinical/scientific integrity of the product and to provide qualitative submissive data
- Develop and write relevant clinical documents such as study protocols, study procedure manuals, informed patient consent, written responses to ethics committees/regulatory authorities, clinical study reports and scientific publications
- Partner with the medical staff and key opinion leaders in immuno-oncology (solid cancers and immunotherapy)
- Provide regular follow-ups and preliminary assessments of clinical results in collaboration with the Clinical Operations Director and Clinical Project Leaders for review and approval
- Write and/or review publications, collaborative abstracts, posters and content for clinical programs, scientific meetings and conferences and contribute to the generation of a communication/publication plan.

**_PROFILE_**

To qualify for the role, you must have:

- A Master degree in Life Sciences (PhD), Pharmacy or Medicine
- At least 5 years’ experience in the development and management of clinical trial projects (CRO or pharmaceutical industry) in oncology, ideally in immuno-oncology (solid cancers and immunotherapies).
- You already have a good deal of knowledge about clinical trial documentation (regulatory, pharmacovigilance) and good clinical practice.
- You have good interpersonal and writing skills. You are autonomous and you show initiative. You contribute to a collective and strong organization.
- Ideally you have an interest for the pharmaceutical or biotech sector.
- You master the language of Voltaire in both written and oral.
- You have a good knowledge of the office pack

Your rigor and enthusiasm will be an asset to succeed in this mission.

This role will allow you to evolve in a caring environment that can leave you autonomy in your missions.

**_Working at MaaT Pharma is: _**

A friendly and stimulating work environment with challenges, within a passionate teamand also the opportunity to develop your skills and grow.

This position is available immediately

If you can demonstrate that you meet the criteria above, please send your professional resume and a cover letter to the HRD: Emmanuel BURKEL

Type d'emploi : Temps plein, CDI

Salaire : à partir de 50 000,00€ par an

Avantages:

- Participation au Transport
- RTT
- Titre-restaurant

Programmation:

- Travail en journée

Types de primes et de gratifications:

- Primes