Conseiller consultant senior F/H
4 weeks ago
PRÉSENTATION
Les conseillers principaux sont des responsables de l’exécution de projets chargés de mettre en œuvre une recherche de synthèse des données probantes méthodologiquement rigoureuse, de superviser le travail du personnel subalterne et de gérer l’ensemble du projet. Ils travaillent de manière indépendante et en équipe, agissent sur les besoins anticipés du projet et les problèmes à résoudre. Les conseillers principaux doivent interagir avec les clients, comprendre leurs besoins et les exigences de l’industrie et concevoir des projets applicables.
CONNAISSANCES REQUISES
Excellente connaissance des méthodes de revue systématique de la littérature (RSL) et de comparaison indirecte des traitements, y compris la méta-analyse en réseau (MAR) et la comparaison indirecte ajustée par correspondance (CIAC). p>
RESPONSABILITÉS
- Concevoir des études de synthèse des données probantes conformes à l’ETS, gérer des projets et élaborer des produits livrables
- Capacité exceptionnelle à comprendre les modèles d’études observationnelles et d’essais et à interpréter les résultats statistiques dans les articles publiés
- Synthétiser les données qualitativement et quantitativement
- Gérer le personnel pour garantir un travail de haute qualité et dans les délais et examiner en détail le travail produit
- Soutenir le personnel plus expérimenté sur des initiatives commerciales spécifiques, selon les besoins
- Travailler sans supervision de manière indépendante et/ou au sein d’une équipe de projet sur des tâches définies
- Travailler efficacement sur plusieurs fuseaux horaires au sein d’une équipe mondiale
QUALIFICATIONS, EXPÉRIENCE, COMPÉTENCES TECHNIQUES ET PERSONNELLES
- Maîtrise (obligatoire) ou Doctorat (préférable) en épidémiologie, pharmacologie, santé publique ou biostatistique (autres sciences de la santé acceptables)
- 5 ans ou plus d’expérience dans la recherche en synthèse des données probantes, de préférence dans le domaine du conseil, de l’industrie pharmaceutique ou d’autres secteurs de la santé, ou encore le monde universitaire
- Expérience substantielle dans la conduite indépendante de méta-analyses et de CIT dans au moins 1 langage de programmation
- 2 ans ou plus d’expérience en tant que point de contact client et gestion de la livraison/mise en œuvre de ces projets
- Connaissance approfondie de la synthèse des données probantes
- Attention exceptionnelle aux détails
- Excellente rédaction scientifique et logique, avec des résumés de conférence et des manuscrits en tant que premier auteur
- Forte capacité à vérifier la qualité de son propre travail et de celui des autres afin que les brouillons soient livrés avec seulement un minimum d’erreurs typographiques mineures
- Maîtrise de l’anglais (parlé et écrit)
- Un engagement à travailler en collaboration et efficacement avec les autres membres de l’équipe et au sein de l’équipe pour atteindre les objectifs
- Un engagement à communiquer en temps utile en interne et avec les clients
- Une approche pragmatique et logique de résolution de problèmes pour les projets
- Une grande attention aux détails sur tous les produits livrables du projet, même sous la pression de délais courts
- Une bonne compréhension de la gestion de projet avec des compétences éprouvées en matière de gestion du temps et d’organisation personnelle
Senior Consultant, Evidence Synthesis, RWE
OVERVIEW
Senior Consultants are project delivery leaders who are responsible for implementing methodologically rigorous evidence synthesis research, overseeing the work of junior staff, and managing the overall project. They work independently and as part of a team, act on anticipated project needs, and problem solve. Senior Consultants are expected to interact with clients, understand their needs and industry requirements, and design applicable projects.
REQUIRED KNOWLEDGE
Excellent knowledge of systematic literature review (SLR) methods and indirect treatment comparison, including network meta-analysis (NMA) and matching-adjusted indirect comparison (MAIC). p>
RESPONSIBILITIES
- Design HTA compliant evidence synthesis studies, project management, and deliverable development
- Exceptional ability to understand observational and trial study designs, and interpret statistical results in published papers
- Synthesize data qualitatively and quantitatively
- Manage staff to ensure high quality and timely work and review in detail the work that is produced
- Support more senior staff on specific business initiatives as required
- Work without supervision independently and/or as part of a project team on defined tasks
- Work effectively across time zones as part of a global team
QUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLS
- Masters (required) or PhD (preferred) in epidemiology, pharmacology, public health, or biostatistics (other health sciences ok)
- 5+ years of experience of working in evidence synthesis research, preferably in consulting, pharmaceutical or other healthcare industry, academia
- Substantial experience independently conducting meta-analysis and ITC in at least 1 programming language
- 2+ years of experience being the client point of contact and managing the delivery/implementation of those projects
- Expert knowledge of evidence synthesis
- Exceptional attention to detail
- Strong scientific and logical writing with a track record of first author conference abstracts and manuscripts
- Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors
- Fluency in English (spoken and written)
- A commitment to working collaboratively and effectively with others in and across the team to accomplish goals
- A commitment to timely internal and client communication
- A pragmatic and logical problem solving approach to projects
- Strong attention to detail on all project deliverables even under time pressure
- A good understanding of project management with proven time management and personal organizational skills
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