Presentation

Les assistants principaux de recherche clinique sont des experts en methodologie disposant d’une vaste experience dans la prestation de services de consultation aux clients pharmaceutiques. Les assistants principaux sont des chefs de projet charges de mettre en œuvre une recherche rigoureuse de synthese des donnees probantes, de superviser le travail du personnel subalterne et de gerer de maniere proactive le calendrier du projet. Ils sont soucieux du detail, agissent sur les besoins anticipes du projet et resolvent les problemes. Les assistants principaux contribuent a la bonne sante operationnelle et financiere de la pratique globale et a la formation/reussite du personnel subalterne.

Overview

Associate Principals are methodologic experts with substantial experience in providing consulting services to pharmaceutical clients. Associate Principals are project leaders who are responsible for implementing rigorous evidence synthesis research, overseeing the work of junior staff, and proactively managing the project timeline. They are detail oriented, act on anticipated project needs, and problem solve. Associate Principals contribute to the operational and fiscal health of the overall practice and training/success of junior staff.

Connaissances requises

Excellente connaissance des methodes de revue systematique de la litterature (RSL) et de comparaison indirecte des traitements (CIT). Experience significative dans la direction et la conduite de projets CIT, y compris une meta-analyse en reseau, une meta-analyse en appariement ajuste, etc. Comprehension experte des directives et des meilleures pratiques mondiales en RSL, et experience substantielle dans leur mise en œuvre.

Required Knowledge

Excellent knowledge of systematic literature review (SLR) methods and indirect treatment comparison (ITC). Significant experience leading and conducting ITC projects, including network meta-analysis, matching adjusted meta-analysis, etc. Expert understanding of global SLR guidelines and best practices, and substantial experience in implementing them.

Responsabilites

• Diriger la mise en œuvre de projets de synthese des donnees probantes pour soutenir les soumissions d’ETS et/ou reglementaires, depuis la preattribution jusqu’a la livraison finale, ainsi que le developpement pratique des livrables.
• Diriger les equipes de projet pour assurer l’execution de livrables rigoureux et de haute qualite selon les echeanciers.
• Capacite d’expert a synthetiser des donnees qualitativement et quantitativement et a guider le personnel subalterne.
• Gestion de projet : gerer des projets, superviser les exigences operationnelles, financieres et administratives des projets.
  
  
  
  
• Developpement commercial : qualifier les prospects de maniere independante, elaborer des propositions, assister aux defenses des offres et gerer le processus de passation des marches.
• Soutenir le personnel plus experimente sur des initiatives commerciales specifiques, selon les besoins.
• Travailler efficacement sur plusieurs fuseaux horaires au sein d’une equipe mondiale.

Responsibilities

• Lead implementation of evidence synthesis projects to support HTA and/or regulatory submissions from pre-award to final delivery, as well as hands on development of deliverables.
• Lead project teams to ensure the execution of rigorous and high quality deliverables according to timelines.
• Expert ability to synthesize data qualitatively and quantitatively, and guide junior staff.
• Project management—manage projects, oversee the operational, financial, and administrative requirements of projects.
• Business development—independently qualify leads, develop proposals, attend bid defenses, and manage the contracting process.
• Support more senior staff on specific business initiatives as needed.
• Work effectively across time zones as part of a global team.

Client management

• Must have 5+ years as the point of contact on projects.

Qualifications, Experience, Technical and Personal Skills

• Masters in epidemiology, pharmacology, public health, or biostatistics (other health sciences ok).
• 7+ years leading the implementation of evidence synthesis research (must have a strong background in biostatistics).

Preferred Experience

• PhD in epidemiology, public health, or biostatistics (other health sciences ok).
• 5+ years leading the implementation of evidence synthesis research (must have a strong background in biostatistics).

Essential General Technical Skills And Knowledge

• Exceptional attention to detail.
• Significant and demonstrated experience independently leading projects that included Bayesian NMAs and/or other ITCs.
• Solid understanding of SLR concepts, guidelines, and required rigor.
• Substantial experience independently leading projects that included meta-analysis, NMA, or other Bayesian statistical analysis.
  
  
  
  
• Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors.
• Competency in using PowerPoint, Excel, and Word.

Essential Personal Skills And Behaviors

• Fluency in English (spoken and written); strong business/scientific written English.
• 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; with clients, IQVIA project managers and team members, IQVIA colleagues and others.
• 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.

Salary and Perks

La fourchette salariale de base potentielle pour ce poste, annualisee, est de $153,000.00 - $204,000.00. Le salaire de base reel offert peut varier selon plusieurs facteurs, notamment les qualifications liees a l’emploi telles que les connaissances, les competences, la formation et l’experience ; l’emplacement ; et/ou l’horaire (temps plein ou temps partiel). Selon le poste offert, des regimes d’incitation, des primes et/ou d’autres formes de remuneration peuvent etre proposes, en plus d’une gamme d’avantages sociaux lies a la sante, au bien‑etre et/ou d’autres benefices.

Equal Opportunity Employment Statement

IQVIA est fiere d’etre un employeur souscrivant au principe de l’egalite d’acces a l’emploi. Tous les candidats qualifies seront pris en consideration pour un emploi sans egard a la race, la couleur, la religion, le sexe, l’orientation sexuelle, l’identite de genre, l’origine nationale, le handicap, l’age, l’etat matrimonial ou tout autre statut protege par la loi applicable. Des mesures d’adaptation pour les candidats handicapes sont disponibles sur demande dans tous les aspects du processus de recrutement. Si vous avez un handicap qui necessite une mesure d’adaptation, nous vous encourageons a contacter notre equipe d’acquisition de talents au , afin qu’IQVIA puisse soutenir votre participation au processus de recrutement.

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, marital status, or any other status protected by applicable law. Accommodations for applicants with disabilities are available in all aspects of the recruitment process upon request.