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Senior Consultant, Evidence Synthesis, Indirect Treatment Comparison (ITC) (United States)

ダーラム, ノースカロライナ州 Full time R1486985 Home-based

ダーラム, ノースカロライナ州

Build a rewarding career in life sciences consulting and forge your own path. Partner with collaborative teams and leaders across unique projects and geographies, delivering innovative solutions to the most complex healthcare problems along the way. Working at IQVIA means changing outcomes for patients one data set, product offering and innovative solution at a time.

As a Consultant at IQVIA, you'll have the opportunity to grow your career and explore opportunities in brand and integrated research solutions, go-to-market strategy, commercial excellence, real world data, financial investor consulting and more.

応募

Success Profile

IQVIAで活躍しているコンサルタントは? 共通するスキル・マインドセットはこちらです。

  • ACHIEVER
  • COMMUNICATION
  • CRITICAL-THINKER
  • ADAPTABLE
  • STRATEGIC
  • DETAIL-ORIENTED

What you can expect

Professional Development

スキル向上できる環境

Highly Specialized

専門分野に特化した働き方

Growth Potential

ステップアップに向けた明確なキャリアパス

Collaboration

共通の目標に向かって、協力し合うチーム

Innovative Projects

複雑な課題を革新的な方法で解決

Best-in-Class Training

知識とスキルを向上するためのトレーニング

Senior Consultant, Evidence Synthesis, Indirect Treatment Comparison (ITC) (United States)

ダーラム, ノースカロライナ州, アメリカ合衆国 R1486985
応募

Job Description

Location: Remote, candidates must be US based

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. The role requires superb attention to detail, organization skills, and communication skills. 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). Fundamental understanding of SLR guidelines and best practices, and substantial experience in implementing them. Hands on experience conducting ITCs in R, STATA, or SAS is a must. 

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

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

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, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $121,500.00 - $303,700.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.
応募

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