Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis

Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis Richmond, United States of America | Full time | Home-based | R1557737 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.

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.

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 required Work effectively across time zones as part of a global team QUALIFICATIONS, EXPERIENCE, TECHNICAL AND PERSONAL SKILLS Experience Preferred : PhD in epidemiology or biostatistics (other health sciences okay) 5+ years of experience implementing evidence synthesis research in a pharma consulting environment Master's in epidemiology or biostatistics (other health sciences okay) 7+ years of experience implementing evidence synthesis research in a pharma consulting environment Client management Must have 5+ years of experience as the client point of contact on projects Technical skills and knowledge Significant and demonstrated experience independently leading projects that included Bayesian NMAs and/or other ITCs Substantial experience independently leading projects that included meta-analysis, NMA, or other Bayesian statistical analysis Solid understanding of SLR concepts, guidelines, and required rigor Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors Exceptional attention to detail 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 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 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. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $125,800.00 - $350,300.00. 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. Location: Remote, must be based in US

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. 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. 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 required Work effectively across time zones as part of a global team Experience Preferred : PhD in epidemiology or biostatistics (other health sciences okay) 5+ years of experience implementing evidence synthesis research in a pharma consulting environment Master's in epidemiology or biostatistics (other health sciences okay) 7+ years of experience implementing evidence synthesis research in a pharma consulting environment Client management Must have 5+ years of experience as the client point of contact on projects Technical skills and knowledge Significant and demonstrated experience independently leading projects that included Bayesian NMAs and/or other ITCs Substantial experience independently leading projects that included meta-analysis, NMA, or other Bayesian statistical analysis Solid understanding of SLR concepts, guidelines, and required rigor Strong ability to quality check own and others work so that drafts are delivered with only minimal minor typographical errors Exceptional attention to detail 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 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 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. IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. The potential base pay range for this role, when annualized, is $125,800.00 - $350,300.00. 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. Where you'll work Home-based You’ll work remotely, with the flexibility to do your best work from home. Supported by collaborative tools and a global team, you’ll stay connected while enjoying the autonomy and balance that comes with a fully remote role. "I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact. The culture in IQVIA is to be constantly looking at how we can do things better to help our customers, to bring life-changing medicines to patients and also to be a part in designing and developing and implementing these solutions. And so I think it's a great place to join because there is that organizational focus and commitment in driving forward the innovation and just the ability, I think, to work with cross-functional teams who are all excited to be working in these areas. It's a fantastic opportunity. First of all, we are humans, we have some moments in our lives that are so very important and we need to respect. And something I also always love about IQVIA was that my leaders and people with which I have been working, they always respected a lot as well our personal lives. I never miss a parents' meeting of my kids, and this is something that we shouldn't be giving for granted. Senior Director Global Site Activation "I like that we're different. I like that we're a unique organization unlike any other. I like to think of us as the intelligence company for life sciences and healthcare. I do believe there's nothing else like this organization in the world. So if you like something that's different and interesting, you're going to like IQVIA. If you like an organization that has a variety of opportunities, from IT to big data to AI to finance to HR, there are so many opportunities to have an impact. Culture Culture at IQVIA is built on a shared belief: that when people are empowered with better data, smarter technology and deeper expertise, they can change what’s possible for patients. Across every team and every corner of the globe, you’ll find colleagues who genuinely care — about the mission and about each other. That’s what makes this a place where people tend to stay, grow and do the best work of their careers. Associate Principal, Indirect Treatment Comparison (ITC), Evidence Synthesis Richmond, United States of America | Home-based #J-18808-Ljbffr IQVIA Argentina