Spécialiste Etudes Cliniques Et Facteurs Humains Dispositif Médicaux

**Job Description Summary**: Are you looking for a challenging role in the medical industry where you can actively contribute to the clinical and human factors studies for medical devices ?

With innovative pre-fillable syringes, self-injection systems, safety systems and needle technologies, the Pharmaceutical Systems (PS) team offer an extensive selection of solutions designed to protect, package and deliver drug therapies.

**We are the makers of possible**:
BD is one of the largest global medical technology companies in the world. Advancing the world of health is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.

**Why Join Us?**

A career at BD means learning and working alongside inspirational leaders and colleagues who are equally passionate and committed to fostering an inclusive, growth-centered, and rewarding culture. You will have the opportunity to help shape the trajectory of BD while leaving a legacy at the same time.

To find purpose in the possibilities, we need people who can see the bigger picture, who understand the human story that underpins everything we do. We welcome people with the imagination and drive to help us reinvent the future of health. At BD, you’ll discover a culture in which you can learn, grow and thrive. And find satisfaction in doing your part to make the world a better place.

Become a maker of possible with us

**Responsibilities**:

- MSA representative for the Human factors and Clinical expertise in CoreTeam.
- MSA voice ensuring the safety and performance od BDM-PS products in his/her scope.
- Help write and update the Clinical Development Plans.
- Contributing to developing evaluation of BD products (methods and capabilities) to assess end-users’ acceptance, preference, and willingness to adopt the medical device.
- Work with the team to establish a budget and timeline for the study.
- Assist in selecting and evaluating proposals from study suppliers and train the chosen supplier.
- Help complete the final study report and contribute to writing scientific publications.
- Support the team as needed to ensure the success of the study.
- Responsible for Design Control deliverables in his/her scope.
- Participation in promotional material review technical training modules on products in his/her scope.
- Interacts with customers when relevant.
- Works cross-functionally to collect inputs necessary for decision making.

**Preferred Requirements**:

- Master’s degree in bio-technologies or medical field
- Good understanding of clinical studies set-up (ideally studies to assess end-users' acceptance and product usability)
- Self-starter with excellent organizational and communication skills
- Ability to work effectively in a dynamic and fast-paced environment with cross-functional teams
- English

Becton, Dickinson and Company is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.

**Required Skills**:
Optional Skills


**Primary Work Location**: FRA Le Pont-de-Claix Cedex

**Additional Locations**:
**Work Shift**: