Clinical Scientist- R&D Pharma - CDI- F/M

Pierre Fabre Laboratories; Occitanie; Hybrid; EUR 70,000 - 100,000; Full time

Benefits offered by this job

Incentives

Profit-sharing

Health insurance

Provident insurance

Public transport subsidy

RTT 16 days

25 days personal holidays

Job summary

Pierre Fabre Laboratories is seeking a Clinical Scientist- R&D Pharma to support oncology clinical development. Based in Toulouse, you will contribute to investigator relationships, data analysis, and submission documents, while driving medical monitoring and cross-functional collaboration.

Join a global leader committed to science, human care, and a flexible teleworking arrangement up to two days per week, with a comprehensive remuneration and benefits package.

Qualifications

• Advanced degree in a scientific discipline (e.g. PhD, PharmD, NP, PA, or equivalent).
• Oncology field experience and understanding of clinical development.
• At least 3 years of Pharma R&D experience and strong English communication.

Responsibilities

• Provide insights in internal study meetings, investigator interactions, and data reviews.
• Support study design, clinical documents, and regulatory submissions.
• Collaborate with Medical Monitors, Clinical Operations, and CROs to ensure program alignment.

Skills

Advanced degree

Oncology experience

Pharma R&D experience

English proficiency

Education

Advanced scientific degree

Job description

Who we are ?

We are Pierre Fabre Laboratories, a global leader combining pharmaceutical expertise with dermo-cosmetics to support consumers and patients at every stage of their care journey.
Our portfolio includes several medical franchises and international brands such as Eau Thermale Avène, Ducray, A-Derma, Klorane, René Furterer, and Pierre Fabre Oral Care.
By joining us, you become part of a meaningful company where the human dimension is essential. You become a participant in the "We Care Movement," a movement that values excellence and innovation within passionate teams. Together, we push the boundaries of science to unite health and beauty for the benefit of all, because Every time we care for a single person, we make the whole world better.

Present in 120 countries with a team of over 10,000 employees, we are proud to create a scientific and human impact, today and tomorrow! If caring is at the heart of your values, join Pierre Fabre Laboratories and become a key player in the "We Care Movement".

Your mission

We are looking for a Clinical Scientist- R&D Pharma to support Clinical Medical Monitoring activities in the framework of clinical trial development in oncology.

The Clinical Development team is based in Toulouse (Langlade) and focuses on oncology clinical development, strategic assessments and support to clinical trials.

In this position, you will support Pierre Fabre clinical team and development function through knowledge of investigator relationships and analysis of the clinical trials data.

Your role within a pioneering company in full expansion:

At study level, and as directed, provide insights in internal study level meetings, investigator interactions, medical data review, curation and interpretation of aggregate PD, PK, efficacy, safety data, and as requested, contribute to author/review of study-related documents and submissions.

Strategic Contributions:

• Collaborate with the Clinical Development Director to synthesize literature, preclinical data, regulatory guidance, and clinical insights to build program rationale.

• Support the Clinical Development Director in proposals at advisory boards, investigator meetings, and site initiations.
• Stay current with the clinical landscape by attending scientific and clinical conferences.

Clinical Study Support:

• Contribute to study design and develop clinical documents (e.g., protocols, investigator brochures, informed consent forms, study manuals, clinical study reports).
• Work closely with Medical Monitors and Clinical Operations to address protocol questions from health authorities and ethics committees.
• Participate in clinical site and vendor selection.
• Provide clinical status updates and build collaborative relationships with investigators and key opinion leaders (KOLs).

Operational Excellence:

• Assist in organizing clinical meetings (e.g., advisory boards, data safety monitoring boards, and steering committees).
• Engage with Clinical Operations for site start-up, engagement, and recruitment.
• Support medical monitoring activities, and data quality reviews

Cross-Functional Collaboration:

• Act as a task force leader for best practices or special initiatives.
• Represent the asset team at governance reviews and present on special topics.
• Work closely with external consultants, regulatory teams, and CROs to ensure program alignment.

This position is compatible with teleworking up to 2 days a week according to company rules.

We offer an attractive remuneration/benefits package: Incentives, profit-sharing, Pierre Fabre shareholding with matching contribution, health and provident insurance, 16 days of holidays (RTT) in addition to 25 days of personal holidays, public transport participation…

Who you are ?

Your skills at the service of innovative projects:

• Advanced degree in a scientific discipline (e.g. PhD, PharmD, NP, PA, or equivalent)
• Oncology Field
• 3 years of experience with Pharma R&D
• Proficiency in English (written and spoken)

At Pierre Fabre Laboratories, we believe that our greatest asset is our people.

We are committed to a policy of Equal Employment Opportunity and will not discriminate against an applicant or employee based on race, color, religion, creed, national origin or ancestry, sex, sexual orientation, gender identity or expression, age, physical or mental disability, veteran or military status, genetic information, or any other legally recognized protected basis under federal, state, or local law. The information collected by this application is solely to determine suitability for employment, verify identify, and maintain employment statistics on applicants. Applicants with disabilities may be entitled to reasonable accommodation under the Americans with Disabilities Act and certain state or local laws. Please inform the company's personnel representative if you need assistance completing this application or to otherwise participate in the application process. Thus, we commit to considering all applications equally, without fail.