Manager, Clinical Site Centricity
AbbVie
Manager, Clinical Site Centricity
Job Description
AbbVie is committed to being an industry leader in accelerating the transformation of molecules to medicines to maximize the value for patients and AbbVie. Clinical Site Centricity drives the collection, synthesis, and action planning around site feedback and the strategic communications infrastructure that contributes to strengthening the partnership between AbbVie and our clinical trial sites. The Manager, Clinical Site Centricity sits within the Clinical Development Operations (CDO) organization. This role will report into the Director, Clinical Site Centricity.* This role requires onsite work at AbbVie locations. The expected onsite days are Tuesday, Wednesday, and Thursday each week. Illinois (IL): North Chicago, Massachusetts (MA): Worcester, New Jersey (NJ): Branchburg, Florham Park, California (CA): Irvine, South San FranciscoContribute to writing qualitative and quantitative insights surveys and discussion guides to solicit insights from clinical sites that support operational excellenceManage the development, programming, and deployment of site-facing surveys such as the Global All Investigator Survey and study surveysWrite materials for internal change management and communications regarding site-facing surveysManage timelines and project related to external benchmarking of AbbVie’s positioning in industry (Centerwatch) Ensure quality in survey implementation, response collection, and data analysis to support data integrityCollaborate with data analytics partners to answer key business questions leveraging survey data and deliver analysesContribute to the advancement of survey implementation technology and analysis including opportunities for software and AI to automate and refine data collection, analysis, and reportingContribute to the development of presentations and tools that enable sharing of strategic insights with internal stakeholders including leadershipSupport template development for Clinical Site Centricity deliverablesManage Sharepoint and playbooks for Clinical Site Centricity TeamEnsure research methods are compliant with all procedures and regulationsSupport supplier oversight in project execution as needed
Locations
- Branchburg, NJ
Salary
106,500 - 202,500 USD / yearly
Estimated Salary Rangemedium confidence
110,000 - 150,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Survey design and development (qualitative and quantitative)intermediate
- Project management and timeline coordinationintermediate
- Data analysis and integrity assuranceintermediate
- Collaboration with analytics partnersintermediate
- Technology advancement in surveys (software, AI automation)intermediate
- Internal communications and change managementintermediate
- Benchmarking and industry positioning analysisintermediate
- Presentation and stakeholder engagementintermediate
- Compliance with research regulationsintermediate
- Supplier oversightintermediate
Required Qualifications
- This role requires onsite work at AbbVie locations (Tuesday, Wednesday, and Thursday each week) in North Chicago, IL; Worcester, MA; Branchburg or Florham Park, NJ; Irvine or South San Francisco, CA (experience)
- Experience in clinical development operations or related field preferred, with knowledge of research methods compliant with procedures and regulations (experience)
Responsibilities
- Contribute to writing qualitative and quantitative insights surveys and discussion guides to solicit insights from clinical sites that support operational excellence
- Manage the development, programming, and deployment of site-facing surveys such as the Global All Investigator Survey and study surveys
- Write materials for internal change management and communications regarding site-facing surveys
- Manage timelines and projects related to external benchmarking of AbbVie’s positioning in industry (Centerwatch)
- Ensure quality in survey implementation, response collection, and data analysis to support data integrity
- Collaborate with data analytics partners to answer key business questions leveraging survey data and deliver analyses
- Contribute to the advancement of survey implementation technology and analysis including opportunities for software and AI to automate and refine data collection, analysis, and reporting
- Contribute to the development of presentations and tools that enable sharing of strategic insights with internal stakeholders including leadership
- Support template development for Clinical Site Centricity deliverables
- Manage Sharepoint and playbooks for Clinical Site Centricity Team
- Ensure research methods are compliant with all procedures and regulations
- Support supplier oversight in project execution as needed
Benefits
- general: Commitment to industry leadership in accelerating transformation of molecules to medicines
- general: Strengthening partnerships between AbbVie and clinical trial sites through strategic communications
Tags & Categories
Manager, Clinical Site Centricity
AbbVie
Manager, Clinical Site Centricity
Job Description
AbbVie is committed to being an industry leader in accelerating the transformation of molecules to medicines to maximize the value for patients and AbbVie. Clinical Site Centricity drives the collection, synthesis, and action planning around site feedback and the strategic communications infrastructure that contributes to strengthening the partnership between AbbVie and our clinical trial sites. The Manager, Clinical Site Centricity sits within the Clinical Development Operations (CDO) organization. This role will report into the Director, Clinical Site Centricity.* This role requires onsite work at AbbVie locations. The expected onsite days are Tuesday, Wednesday, and Thursday each week. Illinois (IL): North Chicago, Massachusetts (MA): Worcester, New Jersey (NJ): Branchburg, Florham Park, California (CA): Irvine, South San FranciscoContribute to writing qualitative and quantitative insights surveys and discussion guides to solicit insights from clinical sites that support operational excellenceManage the development, programming, and deployment of site-facing surveys such as the Global All Investigator Survey and study surveysWrite materials for internal change management and communications regarding site-facing surveysManage timelines and project related to external benchmarking of AbbVie’s positioning in industry (Centerwatch) Ensure quality in survey implementation, response collection, and data analysis to support data integrityCollaborate with data analytics partners to answer key business questions leveraging survey data and deliver analysesContribute to the advancement of survey implementation technology and analysis including opportunities for software and AI to automate and refine data collection, analysis, and reportingContribute to the development of presentations and tools that enable sharing of strategic insights with internal stakeholders including leadershipSupport template development for Clinical Site Centricity deliverablesManage Sharepoint and playbooks for Clinical Site Centricity TeamEnsure research methods are compliant with all procedures and regulationsSupport supplier oversight in project execution as needed
Locations
- Branchburg, NJ
Salary
106,500 - 202,500 USD / yearly
Estimated Salary Rangemedium confidence
110,000 - 150,000 USD / yearly
Source: AI estimated from job description
* This is an estimated range based on market data and may vary based on experience and qualifications.
Skills Required
- Survey design and development (qualitative and quantitative)intermediate
- Project management and timeline coordinationintermediate
- Data analysis and integrity assuranceintermediate
- Collaboration with analytics partnersintermediate
- Technology advancement in surveys (software, AI automation)intermediate
- Internal communications and change managementintermediate
- Benchmarking and industry positioning analysisintermediate
- Presentation and stakeholder engagementintermediate
- Compliance with research regulationsintermediate
- Supplier oversightintermediate
Required Qualifications
- This role requires onsite work at AbbVie locations (Tuesday, Wednesday, and Thursday each week) in North Chicago, IL; Worcester, MA; Branchburg or Florham Park, NJ; Irvine or South San Francisco, CA (experience)
- Experience in clinical development operations or related field preferred, with knowledge of research methods compliant with procedures and regulations (experience)
Responsibilities
- Contribute to writing qualitative and quantitative insights surveys and discussion guides to solicit insights from clinical sites that support operational excellence
- Manage the development, programming, and deployment of site-facing surveys such as the Global All Investigator Survey and study surveys
- Write materials for internal change management and communications regarding site-facing surveys
- Manage timelines and projects related to external benchmarking of AbbVie’s positioning in industry (Centerwatch)
- Ensure quality in survey implementation, response collection, and data analysis to support data integrity
- Collaborate with data analytics partners to answer key business questions leveraging survey data and deliver analyses
- Contribute to the advancement of survey implementation technology and analysis including opportunities for software and AI to automate and refine data collection, analysis, and reporting
- Contribute to the development of presentations and tools that enable sharing of strategic insights with internal stakeholders including leadership
- Support template development for Clinical Site Centricity deliverables
- Manage Sharepoint and playbooks for Clinical Site Centricity Team
- Ensure research methods are compliant with all procedures and regulations
- Support supplier oversight in project execution as needed
Benefits
- general: Commitment to industry leadership in accelerating transformation of molecules to medicines
- general: Strengthening partnerships between AbbVie and clinical trial sites through strategic communications
Tags & Categories