Verified Job
Work from home
Sr Data Team Lead
Work from home
#673998
Remote / WFH
Job Description
**Role Summary**
This role requires **hands-on Veeva Clinical Data Management (CDM) experience** . Candidates must have demonstrated leadership on studies executed in **Veeva Clinical Data** .
+ Preference for experienced **Data Team Lead (DTL)** or **less experienced Senior DTL**
+ **6+ years of Clinical Data Management experience** , with **2–4 years in a lead role**
+ Minimum **2 years leading studies using Veeva CDM required**
+ Proven experience managing end-to-end DM delivery on clinical studies within Veeva
+ Ability to independently lead projects, manage client interactions, and oversee DM teams
+ **Available to start no later than March**
+ Location: **United States or Canada**
• *Core Responsibilities**
+ Provide senior leadership for end‑to‑end Clinical Data Management delivery across multiple studies or global programs, serving as primary client contact and leading negotiations related to timelines, scope, resources, and financials while ensuring strong customer relationships and effective issue escalation.
+ Lead project and service delivery through strategic planning, resourcing, and oversight of DTL and Data Operations teams; ensure quality, timelines, and contractual commitments are met through DMP development and approval, proactive quality management, compliance oversight, and continuous process improvement.
+ Serve as subject matter expert and mentor within the CDM organization, supporting junior DTL development, best practice initiatives, and technology implementation while independently managing budgets, SOWs, financial performance, change orders, RFP support, and broader organizational contributions.
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, ****** 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 $86,800.00 - $217,100.00. 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
• *Role Summary**
This role requires **hands-on Veeva Clinical Data Management (CDM) experience** . Candidates must have demonstrated leadership on studies executed in **Veeva Clinical Data** .
+ Preference for experienced **Data Team Lead (DTL)** or **less experienced Senior DTL**
+ **6+ years of Clinical Data Management experience** , with **2–4 years in a lead role**
+ Minimum **2 years leading studies using Veeva CDM required**
+ Proven experience managing end-to-end DM delivery on clinical studies within Veeva
+ Ability to independently lead projects, manage client interactions, and oversee DM teams
+ **Available to start no later than March**
+ Location: **United States or Canada**
• *Core Responsibilities**
+ Provide senior leadership for end‑to‑end Clinical Data Management delivery across multiple studies or global programs, serving as primary client contact and leading negotiations related to timelines, scope, resources, and financials while ensuring strong customer relationships and effective issue escalation.
+ Lead project and service delivery through strategic planning, resourcing, and oversight of DTL and Data Operations teams; ensure quality, timelines, and contractual commitments are met through DMP development and approval, proactive quality management, compliance oversight, and continuous process improvement.
+ Serve as subject matter expert and mentor within the CDM organization, supporting junior DTL development, best practice initiatives, and technology implementation while independently managing budgets, SOWs, financial performance, change orders, RFP support, and broader organizational contributions.
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, ****** 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 $86,800.00 - $217,100.00. 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This role requires **hands-on Veeva Clinical Data Management (CDM) experience** . Candidates must have demonstrated leadership on studies executed in **Veeva Clinical Data** .
+ Preference for experienced **Data Team Lead (DTL)** or **less experienced Senior DTL**
+ **6+ years of Clinical Data Management experience** , with **2–4 years in a lead role**
+ Minimum **2 years leading studies using Veeva CDM required**
+ Proven experience managing end-to-end DM delivery on clinical studies within Veeva
+ Ability to independently lead projects, manage client interactions, and oversee DM teams
+ **Available to start no later than March**
+ Location: **United States or Canada**
• *Core Responsibilities**
+ Provide senior leadership for end‑to‑end Clinical Data Management delivery across multiple studies or global programs, serving as primary client contact and leading negotiations related to timelines, scope, resources, and financials while ensuring strong customer relationships and effective issue escalation.
+ Lead project and service delivery through strategic planning, resourcing, and oversight of DTL and Data Operations teams; ensure quality, timelines, and contractual commitments are met through DMP development and approval, proactive quality management, compliance oversight, and continuous process improvement.
+ Serve as subject matter expert and mentor within the CDM organization, supporting junior DTL development, best practice initiatives, and technology implementation while independently managing budgets, SOWs, financial performance, change orders, RFP support, and broader organizational contributions.
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, ****** 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 $86,800.00 - $217,100.00. 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
• *Role Summary**
This role requires **hands-on Veeva Clinical Data Management (CDM) experience** . Candidates must have demonstrated leadership on studies executed in **Veeva Clinical Data** .
+ Preference for experienced **Data Team Lead (DTL)** or **less experienced Senior DTL**
+ **6+ years of Clinical Data Management experience** , with **2–4 years in a lead role**
+ Minimum **2 years leading studies using Veeva CDM required**
+ Proven experience managing end-to-end DM delivery on clinical studies within Veeva
+ Ability to independently lead projects, manage client interactions, and oversee DM teams
+ **Available to start no later than March**
+ Location: **United States or Canada**
• *Core Responsibilities**
+ Provide senior leadership for end‑to‑end Clinical Data Management delivery across multiple studies or global programs, serving as primary client contact and leading negotiations related to timelines, scope, resources, and financials while ensuring strong customer relationships and effective issue escalation.
+ Lead project and service delivery through strategic planning, resourcing, and oversight of DTL and Data Operations teams; ensure quality, timelines, and contractual commitments are met through DMP development and approval, proactive quality management, compliance oversight, and continuous process improvement.
+ Serve as subject matter expert and mentor within the CDM organization, supporting junior DTL development, best practice initiatives, and technology implementation while independently managing budgets, SOWs, financial performance, change orders, RFP support, and broader organizational contributions.
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, ****** 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 $86,800.00 - $217,100.00. 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.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
