Senior Research Scientist

il y a 3 semaines

IvrysurSeine, France Thermo Fisher Scientific Temps plein

At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on - now and in the future.

Evidera is a business unit of Pharmaceutical Product Development, LLC (PPD) a leading global contract research organization (CRO), a preeminent provider of evidence-based solutions, and part of Thermo Fisher Scientific.

**Location/Division Specific Information**:
You would be joining a fast growing, successful team, operating at the cutting edge of the science of incorporating stakeholder preferences into health care decision making. We have developed an innovative, collaborative culture, aimed at developing and sharing good practice in preference research, both internally and externally. We are looking for someone who will thrive in this environment.

**Position Location**: Office-based, hybrid or fully remote.

**Discover Impactful Work**:
**A day in the Life**:
**Science**:

- Applies knowledge of scientific methods, including quantitative and qualitative techniques, with mastery of one area
- Provides scientific leadership to patient preference team members
- Maintains line of research and expertise in relevant scientific areas, along with connections with new literature and regulatory documents
- Publishes scientific work in journals, presents same at professional meetings and is contributing member to professional organizations
- Supports new product development/scientific innovation

**Strategy/Consulting**:

- Consults on strategic insights for patient preference inclusions in drug development
- Plans strategic directions for the group
- Provides rigorous client deliverables
- Develops and maintains client relationships

**Financial & Business Development**:

- Brings in leads and closes sales
- Assumes significant responsibility for sales targets and client development
- Responsible for ongoing stream of funded work for self and others
- Contributes to patient preference financial performance through contribution to funding stream and work allocation.

**Project Management**:

- Manages financial performance of projects and provides guidance to others of same
- Develops proposals, drafting complex steps for scientific integrity to ensure methodological and strategic aspects

**Operations Support**:

- Conducts internal scientific trainings
- Supervises/mentors mid-level scientific staff
- Participates in staff recruitment efforts

**Key Performance Metrics**:

- External recognition as patient preference expert
- Recognition by clients as a key resource for methodology/disease area, publications, and presentations
- Sales credits on projects and contribution to proposals
- Contributions to strategic directions for the patient preference group

**Management Responsibilities**:
May have line-management responsibilities for employees (up to and including Research Scientist)

***:
**Keys to Success**:
**Education**:

- MS/MA/PhD/DrPh/PharmD in a scientific discipline

**Experience**:

- MS/MA more than 15 years’ experience in a relevant field or PhD/DrPH/PharmD + more than 7 years’ experience in a relevant field

**Knowledge, Skills, Abilities**:

- Deep understanding of the positioning of patient preference value messages for growing market
- Knowledge of patient preference needs across drug and medical device development
- Extensive knowledge of methods, pharma and regulatory strategy, pharmaceutical and biotech product development process
- Global regulatory requirements related to health outcomes and preference elicitation, and practical research implementation
- Key aspects of the literature (historical and current), and relevant methodology and statistics
- Ability to critically review literature and contribute successfully to peer-reviewed literature in patient preferences
- Extensive knowledge of drug development process and the regulatory requirements to develop patient preference strategies
- Comprehensive knowledge of patient preference research and demonstrated ability to develop patient preference solutions to client issues
- Ability to supervise, mentor, and review junior level staff
- Possess skills for establishing new and maintaining existing client relationships
- Possess excellent communication skills, including strong presentation abilities

**Physical Requirements / Work Environment**:

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