Clinical Scientist

Resilience; Marseille; Hybride; EUR 50 000 - 80 000; Plein temps

Résumé du poste

Resilience is seeking a Clinical Scientist to drive the success of clinical studies in oncology and chronic diseases. This hybrid role requires strong project leadership and scientific rigor, collaborating with various stakeholders to ensure quality and impact in clinical research.

Qualifications

• 4+ years of experience in clinical research, including study design and management.
• Strong knowledge of GCP, real-world data, and outcomes research.
• Background in oncology or chronic disease management is a plus.

Responsabilités

• Lead the planning, implementation, and management of clinical studies.
• Ensure alignment with timelines, budgets, and regulatory standards.
• Prepare and lead regulatory submissions to health authorities.

Connaissances

Scientific communication

Problem-solving

Project leadership

Adaptability

Formation

PharmD, PhD, or MSc in Life Sciences

Description du poste

What you'll 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 activities—including clinical research, real-world evidence (RWE), and patient support programs (PSP)—we’re 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 Resilience's programs.

Your daily responsibilities & routine:

• 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 committees.
• Act as primary contact for CROs, investigators, pharma partners, and ethics committees.
• 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.
• 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.
• 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.

What you'll bring

You'll 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!

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 [e-mail]

For more information, please check our privacy policy.

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