Senior Clinical Development Scientist

buscojobs España; Barcelona; Presencial; EUR 40.000 - 70.000; Jornada completa

Descripción de la vacante

Una importante empresa busca un profesional experimentado para unirse a su equipo Global Project y Strategic Clinical Team. El candidato ideal deberá tener una licenciatura en ciencias de la vida y más de 3 años de experiencia en la industria farmacéutica, contribuyendo al desarrollo de planes clínicos y documentos relacionados.

Formación

• Más de 3 años de experiencia en la industria farmacéutica en desarrollo de medicamentos.
• Fluidez en inglés (escrito y hablado).
• Experiencia previa en inmunología o dermatología se considera.

Responsabilidades

• Miembro del equipo de estudio clínico, desarrolla documentos de estudios desde el concepto hasta la aprobación.
• Participa en el análisis de datos y en la preparación de convenciones para el DRM.
• Proporciona actualizaciones científicas sobre el estado de la enfermedad.

Conocimientos

Análisis de datos

Comunicación

Presentación

Liderazgo

Educación

Licenciatura en ciencias de la vida o equivalente

PhD o maestría en Medicina Farmacéutica

Herramientas

MS Office

Descripción del empleo

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Mission

Tasks and Responsibilities

Core member of the Global Project Team and Strategic Clinical Team.

Supports the GCPL on the design of clinical development plans (focus on critical review of studies from competitors and aiming to optimize the clinical quality of the clinical design) for internal assets.

Provides regular scientific disease state updates, monitoring of the scientific aspects of the competitive landscape (maintain the scientific updates of competitors in targeted indications which will be the basis for Early Disease Roadmaps (EDR) and Target Product Profile (TPP) definition).

Core member Clinical Study Team.

Works cross-functionally within project/study teams to ensure the clinical strategy is translated into the development of the study concept document/synopsis, study protocol and related documents.

Leads the development of the clinical study synopsis with guidance from GCPLs or delegate and is responsible for accuracy of the scientific content of the study protocol, amendments, CSRs, ICF, CRF, as well as scientific/clinical content of key internal or external project-related documents (e.g., IB, Biomarker Strategy, briefing package for regulatory authorities, responses to Health Authorities for registration purposes and clinical studies approvals, ISE, ISS, publication).

Participates in Data Monitoring Committees.

Provides support for the definition and review of protocol deviations and leads the preparation of the conventions for the DRM. Supports the GCPL in data analysis and data review.

Participates in data analysis and provides support for content proposals for publications.

Education

• Bachelor’s degree in life sciences or equivalent (e.g., Pharmacy, Biology, Molecular Medicine, Bioengineering).
• Advanced Degree (PhD or master’s degree in Pharmaceutical Medicine) valuable.
• Prior experience in immunology or dermatology may be also considered.
• More than 3 years of Pharmaceutical Industry experience in drug development, including experience in Health Authorities consultancies and having contributed to MAA submission to the Health Authorities.
• Demonstrates understanding of methodology in the design, conduct, review and interpretation, and presentation of clinical research.
• Fluency in English (written and spoken), proficiency with MS Office.

Specific Knowledge

• Data analysis, communication, and presentation skills in team settings and in formal presentations to leadership committees both internally and externally.
• Leadership skills with the ability to influence others and drive consensus building.