Job Title: Global Services Coordinator Literature Review
¿Tiene las siguientes habilidades, experiencia e impulso para tener éxito en este puesto? Descúbralo a continuación.
Location: Barcelona (Sant Cugat), Spain – Flexible working options available.
Overview
The Global Services Coordinator Literature Review will be responsible for ensuring the timely and high‑quality delivery of literature review projects (including systematic and targeted literature reviews) and evidence syntheses, ensuring scientific rigor, operational excellence, and alignment with BI’s global standards.
Tasks & Responsibilities
Oversee and deliver timely, high‑quality literature review projects, ensuring compliance with scientific, regulatory, and company standards
Serve as an active member of the literature review governance taskforce, contributing to the definition, implementation, and optimization of processes and standards
Develop and optimize processes, SOPs, and training materials for literature review operations; guide and support team members, providing subject‑matter expertise and training to ensure best practices
Act as the main contact for internal stakeholders, addressing questions, resolving issues, and facilitating smooth project execution
Monitor workload, identify resource needs, and collaborate with fellow Coordinators and Team Lead to address gaps and drive continuous improvement
Foster a collaborative, innovative team environment, sharing expertise and encouraging knowledge exchange
Requirements
Advanced degree (PhD, Master’s, or Bachelor’s) in a relevant scientific field, with 5+ years (PhD/Master’s) OR 8+ years (Bachelor’s) of experience in systematic literature review methods in the pharmaceutical, biotech, or consulting setting
Experience in conducting different types of systematic and targeted literature reviews (clinical, economic, QoL, burden of illness, etc.) and knowledge of statistical software (e.g., RevMan, Stata, R, Comprehensive Meta‑Analysis) to conduct meta‑analyses
Demonstrated organizational and project‑management experience coordinating operational tasks and group workload; strong stakeholder engagement and effective communication skills; ability to manage multiple projects simultaneously in a fast‑paced environment
Fluent in English with excellent written and verbal communication xpzdshu skills
Knowledge of value dossier writing requirements, global HTA bodies submission requirements, pharmacoeconomic publication writing, and related deliverables is desirable
Prior experience working in any of the therapeutic areas of Cardiovascular Renal Metabolism (CRM), Respiratory, Inflammation, Immunology, or Oncology would be advantageous
Benefits
Flexible working conditions
Life and accident insurance
Health insurance at a competitive price
Investment in your learning and development
Gym membership discounts
Job Details
Seniority level: Mid‑Senior level
Employment type: Full‑time
Job function: Other
Industries: Pharmaceutical Manufacturing
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