Senior Quantitative Researcher, Patient Reported Outcomes, Life Sciences
PurposeThe Senior Quantitative Researcher plays a key role in ensuring the scientific development of QualityMetric s world-class health assessment products and conducting strategic projects.
This position supports patient-based outcomes research (e.
g.
, quality of life, functional status assessment, disability, satisfaction, etc.
) for client-sponsored and internally funded projects.
The Senior Quantitative Researcher acts as a lead for proposal and project completion, including identifying a client's needs and conceptualizing and executing a logical design to meet those needs; negotiating ongoing adjustments in the design through internal and external communications.
Senior Quantitative Researchers are responsible for leading study teams on a methodologically diverse portfolio of projects, ranging from small, rapid turnover projects to large, multi-phase or complex projects.
Typically, 65-70% of work effort is towards billable projects (unless candidate assumes large business development or management role).
ResponsibilitiesResponsible for all final project deliverables for which they are PI in terms of accuracy, quality, timelines, financial project performance, and ensuring the content and format are in line with the contracted scope and tailored for the target audienceInteracts with clients, clinical experts, and research support staff to ensure that projects are completed in a timely fashion and in accordance with quality standardsManages projects efficiently and effectively within guidelines of company and department operating proceduresDesigns studies, supervises the development of study materials, manages large data sets, analyzes data, interprets and reports results, and ensures adequate quality assurance is employed throughout the course of the projectPrepares technical reports, summaries, protocolsPrepares and publishes scientific abstracts, posters, reports and manuscriptsPrepares and presents at professional meetings and client-sponsored eventsMaintains substantial knowledge of state-of-the-art principles and theory, as well as current science literatureDelegates work as needed, provides project-specific supervision and training/mentoring to junior-level staffProactively problem solves; identifies and helps drive resolution of issues at all phases of the project that could affect successInteracts effectively and collegially with all employees, fostering a supportive and cross departmental sharing environmentResponsible for a moderate amount of participation in business development activities, including client calls and proposalsQualificationsEducation:
PhD in a relevant field and 5
years post-doctoral work experience (or Master s for outstanding candidates with 8
years of relevant work experience)
Experience:
Acted in lead role (i.
e.
principal investigator) for multiple, complex projectsProficient in SAS (or SPSS, or similar statistical software), MS Office (Word, Excel, PowerPoint); experience with bibliographic software, such as CitaviProven scientific track record:
At least 10 abstracts accepted for presentation, must have presented at least 5 of these at a major scientific venue, or equivalent experience teaching college-level curriculum or industry workshopsAt least 5 peer-reviewed published articles, lead author on at least 2 (abstracts not included; can be in press ), or equivalent experience (such as large number of complex unpublished technical reports for clients, internal statistical manuals or documentation, etc.
)Knowledge:
Applied knowledge of FDA and other industry guidance documents pertaining to the use of patient-reported outcomes (PROs) in medical product development to support labelling claimsStrong background in measurement and quantitative methods, including ability to design study protocols, manage large data sets, analyze data, interpret results and to oversee work of junior-level staffAdvanced knowledge of state-of-the-art principles and theory, as well as current science literatureKnowledge of ICH GCP, 21 CFR Part 11 compliance or experience working in a highly regulated industrySkills:
Strong work ethic, ability to work independently, and demonstrated organizational skillsStrong written and verbal communication skills are required; conveys messages and directions clearly, accurately, and concisely; work requires few clarifications/editionsAbility to work collaboratively in a cross-functional team environmentStrong understanding of client needs and ability to communicate with clientsProven ability to translate knowledge of client needs into scientifically sound and successful proposals and projectsProven track record in meeting deadlines and managing multiple priorities, including exceptional follow-throughTravel requirements:
Approximately 2-4 trips per year to home office in Johnston, RI (for telecommuters) or to relevant conferences for training#ISPOR2024IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.
The potential base pay range for this role, when annualized, is $154,600.
00 - $233,000.
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.
SummaryLocation:
Wayne, PA, United States of America; Falls Church, VA; Durham, NCType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
This position supports patient-based outcomes research (e.
g.
, quality of life, functional status assessment, disability, satisfaction, etc.
) for client-sponsored and internally funded projects.
The Senior Quantitative Researcher acts as a lead for proposal and project completion, including identifying a client's needs and conceptualizing and executing a logical design to meet those needs; negotiating ongoing adjustments in the design through internal and external communications.
Senior Quantitative Researchers are responsible for leading study teams on a methodologically diverse portfolio of projects, ranging from small, rapid turnover projects to large, multi-phase or complex projects.
Typically, 65-70% of work effort is towards billable projects (unless candidate assumes large business development or management role).
ResponsibilitiesResponsible for all final project deliverables for which they are PI in terms of accuracy, quality, timelines, financial project performance, and ensuring the content and format are in line with the contracted scope and tailored for the target audienceInteracts with clients, clinical experts, and research support staff to ensure that projects are completed in a timely fashion and in accordance with quality standardsManages projects efficiently and effectively within guidelines of company and department operating proceduresDesigns studies, supervises the development of study materials, manages large data sets, analyzes data, interprets and reports results, and ensures adequate quality assurance is employed throughout the course of the projectPrepares technical reports, summaries, protocolsPrepares and publishes scientific abstracts, posters, reports and manuscriptsPrepares and presents at professional meetings and client-sponsored eventsMaintains substantial knowledge of state-of-the-art principles and theory, as well as current science literatureDelegates work as needed, provides project-specific supervision and training/mentoring to junior-level staffProactively problem solves; identifies and helps drive resolution of issues at all phases of the project that could affect successInteracts effectively and collegially with all employees, fostering a supportive and cross departmental sharing environmentResponsible for a moderate amount of participation in business development activities, including client calls and proposalsQualificationsEducation:
PhD in a relevant field and 5
years post-doctoral work experience (or Master s for outstanding candidates with 8
years of relevant work experience)
Experience:
Acted in lead role (i.
e.
principal investigator) for multiple, complex projectsProficient in SAS (or SPSS, or similar statistical software), MS Office (Word, Excel, PowerPoint); experience with bibliographic software, such as CitaviProven scientific track record:
At least 10 abstracts accepted for presentation, must have presented at least 5 of these at a major scientific venue, or equivalent experience teaching college-level curriculum or industry workshopsAt least 5 peer-reviewed published articles, lead author on at least 2 (abstracts not included; can be in press ), or equivalent experience (such as large number of complex unpublished technical reports for clients, internal statistical manuals or documentation, etc.
)Knowledge:
Applied knowledge of FDA and other industry guidance documents pertaining to the use of patient-reported outcomes (PROs) in medical product development to support labelling claimsStrong background in measurement and quantitative methods, including ability to design study protocols, manage large data sets, analyze data, interpret results and to oversee work of junior-level staffAdvanced knowledge of state-of-the-art principles and theory, as well as current science literatureKnowledge of ICH GCP, 21 CFR Part 11 compliance or experience working in a highly regulated industrySkills:
Strong work ethic, ability to work independently, and demonstrated organizational skillsStrong written and verbal communication skills are required; conveys messages and directions clearly, accurately, and concisely; work requires few clarifications/editionsAbility to work collaboratively in a cross-functional team environmentStrong understanding of client needs and ability to communicate with clientsProven ability to translate knowledge of client needs into scientifically sound and successful proposals and projectsProven track record in meeting deadlines and managing multiple priorities, including exceptional follow-throughTravel requirements:
Approximately 2-4 trips per year to home office in Johnston, RI (for telecommuters) or to relevant conferences for training#ISPOR2024IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry.
We believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world.
Learn more at We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities.
IQVIA s ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding COVID-19 vaccination status.
The potential base pay range for this role, when annualized, is $154,600.
00 - $233,000.
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.
SummaryLocation:
Wayne, PA, United States of America; Falls Church, VA; Durham, NCType:
Full time.
Estimated Salary: $20 to $28 per hour based on qualifications.
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