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VP, Patient-Centered Trials

Pharmaceutical Product Development (PPD)

US-NC-Wilmington-Wilmington NC HQ

Develops relationships, processes and new capabilities and/or service offerings that will position PPD as an industry leader in sites and patients. Develops and fosters mutually beneficial relationships with PPD business units and external collaborations to assist in winning new business and execution of existing business. Leads the planning and execution of site collaboration and recruitment strategies and patient-centric trial models to drive forward our site/patients capabilities and service offerings.

Essential Functions and other Job information: Drives greater adoption and optimal utilization cross-company to achieve maximum benefit of recent and future acquisitions in order to ensure PPD is positioned as a leader in sites/patients capabilities and service offerings Develops mixed modality approaches to create greater awareness among all PPD business, operational and functional units to ensure seamless integration and implementation into PPD’s core site selection and activation capability Develop enhanced and meaningful relationships with various site networks and patient advocacy groups worldwide to support patient recruitment Build an accelerated/differentiated model that uses EMR data to pre-identify patients and a new site selection and activation model to reach activation within days not months Supports the development and approval of TU-specific site network strategies and collaborates as appropriate with internal/external colleagues to execute Systematically deploys patient recruitment capabilities (including AES) to power enrollment into ongoing PPD projects with associated changes to the commercial model to allow this to occur Develops and executes on the Patient-Centric trial model , including: Developing a methodology to obtain patient input into protocol design and study feasibility Developing capabilities that optimize the communication/ connection to inform and support patient participation in clinical trials Executes strategies to deliver on decentralized trials making research much more accessible/convenient for more patients Developing an approach to provide data to patients to integrate within their ehealthcare environment Develops key measures of success in order to quantify ROI and inform future strategic planning exercise Develop and execute scientifically-based approaches to drive effective patient recruitment strategiesto ensure diversity and inclusion of subjects in clinical trials on behalf of our customers

*LI-LC1

*LI-remote

Develops relationships, processes and new capabilities and/or service offerings that will position PPD as an industry leader in sites and patients. Develops and fosters mutually beneficial relationships with PPD business units and external collaborations to assist in winning new business and execution of existing business. Leads the planning and execution of site collaboration and recruitment strategies and patient-centric trial models to drive forward our site/patients capabilities and service offerings.

Essential Functions and other Job information: Drives greater adoption and optimal utilization cross-company to achieve maximum benefit of recent and future acquisitions in order to ensure PPD is positioned as a leader in sites/patients capabilities and service offerings Develops mixed modality approaches to create greater awareness among all PPD business, operational and functional units to ensure seamless integration and implementation into PPD’s core site selection and activation capability Develop enhanced and meaningful relationships with various site networks and patient advocacy groups worldwide to support patient recruitment Build an accelerated/differentiated model that uses EMR data to pre-identify patients and a new site selection and activation model to reach activation within days not months Supports the development and approval of TU-specific site network strategies and collaborates as appropriate with internal/external colleagues to execute Systematically deploys patient recruitment capabilities (including AES) to power enrollment into ongoing PPD projects with associated changes to the commercial model to allow this to occur Develops and executes on the Patient-Centric trial model , including: Developing a methodology to obtain patient input into protocol design and study feasibility Developing capabilities that optimize the communication/ connection to inform and support patient participation in clinical trials Executes strategies to deliver on decentralized trials making research much more accessible/convenient for more patients Developing an approach to provide data to patients to integrate within their ehealthcare environment Develops key measures of success in order to quantify ROI and inform future strategic planning exercise Develop and execute scientifically-based approaches to drive effective patient recruitment strategiesto ensure diversity and inclusion of subjects in clinical trials on behalf of our customers

*LI-LC1

*LI-remote

Education and Experience: Bachelor’s degree in scientific or related discipline and previous clinical drug development experience (comparable to15 years) in a CRO or Pharmaceutical industry. A visionary leader with at least 10 years of relevant management experience. Prefer experience with site identification, patient enrollment and/or study start-up tasks.

Knowledge, Skills and Abilities: Advanced leadership skills and executive presence Proven negotation skills and ability to effectively influence executives and other stakeholders Exceptional business acumen with comprehensive understanding of the organization and functional areas Ability to work in a high pressure/time sensitive environment including the ability to handle multiple issues on multiple projects simultaneously Advanced knowledge of strategic planning, budgeting, forecasting and fiscal management Strong organizational agility and demonstrated drive for results Track record of building peer relationships and effective teams with demonstrated global and cultural awareness Expertise motivating and integrating teams, as well as excellent coaching and mentoring skills Analytical skills, excellence in oral and written communications, strong attention to detail, priorization and time management proficiencies Thorough understanding of sponsor/CRO business practices and strong knowledge of PPD operational/financial practices, SOPs, GCPs and FDA/ICH guidelines with the ability to analyze and evaluate processes and procedures

Working Conditions and Environment: Work is performed in an office environment with exposure to electrical office equipment. Occasional drives to site locations, frequent travel both domestic and international.

Education and Experience: Bachelor’s degree in scientific or related discipline and previous clinical drug development experience (comparable to15 years) in a CRO or Pharmaceutical industry. A visionary leader with at least 10 years of relevant management experience. Prefer experience with site identification, patient enrollment and/or study start-up tasks.

Knowledge, Skills and Abilities: Advanced leadership skills and executive presence Proven negotation skills and ability to effectively influence executives and other stakeholders Exceptional business acumen with comprehensive understanding of the organization and functional areas Ability to work in a high pressure/time sensitive environment including the ability to handle multiple issues on multiple projects simultaneously Advanced knowledge of strategic planning, budgeting, forecasting and fiscal management Strong organizational agility and demonstrated drive for results Track record of building peer relationships and effective teams with demonstrated global and cultural awareness Expertise motivating and integrating teams, as well as excellent coaching and mentoring skills Analytical skills, excellence in oral and written communications, strong attention to detail, priorization and time management proficiencies Thorough understanding of sponsor/CRO business practices and strong knowledge of PPD operational/financial practices, SOPs, GCPs and FDA/ICH guidelines with the ability to analyze and evaluate processes and procedures

Working Conditions and Environment: Work is performed in an office environment with exposure to electrical office equipment. Occasional drives to site locations, frequent travel both domestic and international.

Job posted: 2021-03-30

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