Clinical Scientist
Clinical Scientist
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Job Description
1 What youll be doing
Your job
Job Summary:
At Resilience we are reinventing remote patient care for oncology and chronic diseases. As we grow our Life Sciences activitiesincluding clinical research real-world evidence (RWE) and patient support programs (PSP)were building a world-class clinical and medical function.
You will be a key member of the Clinical Development team reporting directly to the Senior Clinical Scientist. You will drive the scientific and operational success of our clinical studies contributing to evidence generation strategies protocol design trial oversight and dissemination of scientific outputs.
This is a hybrid role requiring strong project leadership operational agility and scientific rigor. You will collaborate with external stakeholders (sponsors investigators CROs) and internal teams (life sciences ops product data commercial) to ensure the clinical relevance quality and impact of Resiliences programs.
Your daily responsibilities & routine:
1. Clinical Trial Execution
Lead the planning implementation medical monitoring and management of clinical studies (interventional and non-interventional) from protocol design to close-out.
Ensure alignment with timelines budgets and regulatory standards while maintaining scientific integrity and data quality.
Prepare and lead regulatory submissions to health authorities and ethics committee.
Act as primary contact for CROs investigators pharma partners and ethics committees.
2. Scientific Leadership & Evidence Generation
Support protocol development CRF design study documentation
Contribute to the generation of real-world evidence and scientific publications aligned with the Medical Affairs roadmap.
Draft and review scientific outputs (abstracts posters manuscripts) and support participation in medical conferences.
3. Cross-Functional Collaboration
Partner with Product and Tech teams to align features and data flows with clinical research needs.
Provide scientific support to the commercial and customer success teams enhancing practitioner engagement and adoption.
Participate in expert boards advisory meetings and medical education initiatives.
Close collaboration with the Life Sciences team to provide clinical and methodological expertise on projects with pharmaceutical partners.
4. Process & Operational Excellence
Build and optimize clinical processes and documentation (e.g. SOPs workflows) to scale research operations.
Implement study monitoring tools quality control checkpoints and dashboards for internal alignment.
2 What youll bring
Youll definitely have:
PharmD PhD or MSc in Life Sciences
4 years of experience in clinical research including study design and management
Strong knowledge of GCP real-world data and outcomes research
Proven scientific communication skills and publication experience
Proven expertise in clinical research (GCP data capture study conduct)
Background in oncology or chronic disease management is a plus
You are the right person if you have :
Excellent communication structured thinking and problem-solving abilities
Ability to work autonomously while collaborating cross-functionally
Adaptability and curiosity in a fast-evolving health tech environment
Are fluent in both English and French
It would be good if you had:
Relevant understanding of the clinical research industry & clinical guidelines (ICH-GCP - Good Clinical Practice FDA 21 CFR Part 11 etc.)
Resilience is for you if you...
want to join an ambitious project!
want to have an impact!
want to build the future!
3 Recruitment
Interview 1 with Bertille Senior Clinical Scientist - Screening & first discover
Interview 2 with Arlindo Medical Director - More technical assessment
Interview 3 with Emma Clinical Scientist - Discover your team
Interview 4 with Yasmine or one of her team member - Quality and Regulatory
Interview 5 with Emilie Filoni - Culture Fit
GDPR : Your personal data will be processed for the purposes of recruitment related activities which include setting up and conducting interviews and tests for applicants evaluating and assessing the results thereto and as is otherwise needed in the recruitment and hiring processes. They will be available only for people involved in the process and erased after 2 years of inactivity.
Under GDPR and as Resilience attach great importance to privacy please note that you have the right to request access to your personal data to request that your personal data be rectified or erased. The Data Protection Officer can be contacted at
For more information please check our .
Employment Type
Full-Time
