100 director data products jobs found

Merck Job Description This customer-facing position is responsible for managing our company's Wholesaler/Distributor FeeforService agreements across all Human Health, Oncology, and Vaccine customer channels. It is accountable for utilizing and managing SAP and Microsoft Office, as well as working through thirdparty vendors to support systems such as Integrichain (Scorecard, Order Monitoring, Data Accessibility) and OpenText (LENS) for EDI transaction sets that enable tactical and strategic divisional objectives. In partnership with IAM Pharmacy and Distribution teams, this role provides guidance through the analysis, development, and implementation of channelspecific strategies and processes for the Human Health, Oncology, and Vaccine businesses. The position also leads key OrdertoCash projects that span multiple departments and divisions, and supports strategic priorities and contracting in other channels, as directed by management. Key Responsibilities include but...

Merck Job Description The Executive Director, US Data Strategy is responsible for ensuring Human Health (HH) has an industryleading strategy and approach to sourcing, creating, and activating commercial data assets that inform businesscritical decisions and actions across US business units (Oncology, Vaccines, Pharma, Respiratory, Rare Disease). The leader will create, own, and implement the HH US data asset strategy and innovation agenda across commercial data domains (HCP, consumer, payer, patient, account, engagement, and related sources). The role maximizes the return on HH's substantial annual investment in thirdparty data and unlocks value from firstparty, unstructured data assets while ensuring compliance with applicable US privacy and regulatory requirements. Position Responsibilities: Treat data as a strategic asset to empower the organization to drive innovation, make informed decisions, and create competitive advantage for Human Health (HH) US. Shapes...

Merck Job Description Our US Ophthalmology team is committed to transforming the lives of patients living with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) with a portfolio of two products in the pipeline. We aspire to achieve this through a relentless commitment to patients, innovation, ensuring access to lifechanging therapies, and collaborating with healthcare systems, governments, and payers to make treatments available to those who need them most. Our focus is on patients, scientific rigor, and flawless execution-bringing breakthrough therapies to those who need them. We are passionate about bringing our medicines and vaccines to customers around the world. This is a terrific opportunity for a highly motivated individual to serve as a key team member on the US Ophthalmology marketing team and contribute to our scientific strategic development and key tactics for medical education. The ideal candidate for this role has a...

Merck Job Description Our US Ophthalmology team is committed to transforming the lives of patients living with diabetic macular edema (DME) and neovascular age-related macular degeneration (nAMD) with a portfolio of two products in the pipeline. We aspire to achieve this through a relentless commitment to patients, innovation, ensuring access to lifechanging therapies, and collaborating with healthcare systems, governments, and payers to make treatments available to those who need them most. Our focus is on patients, scientific rigor, and flawless execution-bringing breakthrough therapies to those who need them. We are passionate about bringing our medicines and vaccines to customers around the world. This is a terrific opportunity for a highly motivated individual to serve as a key team member on the US Ophthalmology marketing team and contribute to our scientific strategic development and key tactics for medical education. The ideal candidate for this role has a...

Merck Job Description The Executive Director, US Data Strategy is responsible for ensuring Human Health (HH) has an industryleading strategy and approach to sourcing, creating, and activating commercial data assets that inform businesscritical decisions and actions across US business units (Oncology, Vaccines, Pharma, Respiratory, Rare Disease). The leader will create, own, and implement the HH US data asset strategy and innovation agenda across commercial data domains (HCP, consumer, payer, patient, account, engagement, and related sources). The role maximizes the return on HH's substantial annual investment in thirdparty data and unlocks value from firstparty, unstructured data assets while ensuring compliance with applicable US privacy and regulatory requirements. Position Responsibilities: Treat data as a strategic asset to empower the organization to drive innovation, make informed decisions, and create competitive advantage for Human Health (HH) US. Shapes...

Merck Job Description This customer-facing position is responsible for managing our company's Wholesaler/Distributor FeeforService agreements across all Human Health, Oncology, and Vaccine customer channels. It is accountable for utilizing and managing SAP and Microsoft Office, as well as working through thirdparty vendors to support systems such as Integrichain (Scorecard, Order Monitoring, Data Accessibility) and OpenText (LENS) for EDI transaction sets that enable tactical and strategic divisional objectives. In partnership with IAM Pharmacy and Distribution teams, this role provides guidance through the analysis, development, and implementation of channelspecific strategies and processes for the Human Health, Oncology, and Vaccine businesses. The position also leads key OrdertoCash projects that span multiple departments and divisions, and supports strategic priorities and contracting in other channels, as directed by management. Key Responsibilities include but...

Merck Job Description Dir, Engineering, CMC (DCT) Leader for Biologics The Development and Commercialization Team (DCT) leader isaccountable for delivering a fully integrated stage-appropriate CMC development and commercialization strategy which yields the target commercial product.The specific role will be responsible for advancing the company's biologics portfolio. Correspondingly, the DCT leader will be responsible for delivering world class outcomes in the following areas: Responsible for on-time, end-to end execution of DCT deliverables including - robust processes & analytics, an integrated control strategy, successful tech transfer packages, filing and approval, and a robust commercial supply chain toachieve uninterrupted long-term supply Lead DCT. Critically assesses all team deliverables & fosters a learning and collaborative environment. Prioritizes, interrogates and mitigates risks across all factors that may impact technical, operational...

Wabtec Company Description Evident's Inspection Technologies division is now a part of Wabtec Corporation. Read more. Job Description The Global Product Leader is a critical role within the Evident Test & Measurement Global Product Management & Marketing (PMM) organization.  Reporting to the Director, Global Product Management for the assigned product line, this role is responsible for sustaining and growing the market share of their assigned products or product lines, encompassing connected devices, software, and digital workflow solutions strategies, while maintaining a long-term vision to meet market needs. The Global Product Leader will monitor and report on the development of assigned Product and/or Product Line P&L against targets and key product market share development globally, as well as within regions and targeted market segments.  In this effort, this role will ensure close coordination with the Director, Global Product Management, as well as...

CSL Associate Director, Corporate & External Affairs, R&D Portfolio Position Purpose: The Associate Director, R&D Portfolio Corporate and External Affairs, will lead corporate and external affairs communication strategy for CSL's R&D portfolio pipeline. The successful candidate will be responsible for driving communications for key pipeline milestones and clinical trials. They will serve as a strategic partner on R&D policy. They will lead issues and crisis management related to pipeline. In addition, they will strengthen the company's reputation within the biotech ecosystem and US to enhance and protect CSL's reputation and policy position. Reporting Relationships: Reports to: Head of Corporate and External Affairs, R&D Direct reports to position: 1 Main Responsibilities and Accountabilities: Serve as primary business partner and strategic advisor to SVP, Portfolio Development, SVP, Global Regulatory Affairs &...

CSL The Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. Manages a team of programmers supporting clinical trial and integrated analyses, annual reporting, regulatory responses, publications, HTA requests and other purposes as needed within one or more therapeutic areas. The individual will work closely with the Senior Director, Clinical and Statistical Programming to advance the internal programming environment and statistical programming processes. Works closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. Main Responsibilities Working with the Biometrics Programming Leadership team, assess upcoming activities and resulting resource needs and allocate projects to people to ensure high...

CSL Position Summary: The Associate Director, Statistical Programming provides leadership and expertise in driving the development and maintenance of the CSL statistical programming capabilities which is required to meet regulatory obligations. The individual will work closely with the Director, Statistical Programming to ensure all assigned Statistical Programming tasks are managed to completion. They will work closely with Statisticians to ensure that deliverables provided by internal resources or outside providers (CROs; FSP providers) are accurate and aligned with CSL standards. This individual may manage a Therapeutic Areas (TA) or programs within or across TAs working with the Statistics TA lead to ensure all work required in the TA is completed within the project timelines with high quality. Main Responsibilities and Accountabilities : Working with the Director, Programming to assess upcoming activities and resulting resource needs and ensure high quality,...

Transamerica Job Family Research & Analytics - General About Us At Transamerica, hard work, innovative thinking, and personal accountability are qualities we honor and reward. We understand the potential of leveraging the talents of a diverse workforce. We embrace an environment where employees enjoy a balance between their careers, families, communities, and personal interests. Ultimately, we appreciate the uniqueness of a company where talented professionals work collaboratively in a positive environment - one focused on helping people look forward and plan for the best life possible while providing tools and solutions that make it easier to get there. Who We Are We believe everyone deserves to live their best life. More than a century ago, we were among the first financial services companies in America to serve everyday people from all walks of life. Today, we're part of an international holding company, with millions of customers and...

CSL Job description Senior Director Clinical Program Lead CVR You will be accountable for the design and execution of the clinical strategy to support the development of a medicine, aligned with the Project Strategy Document (PSD) and the Target Product Profile (TPP). You are also accountable for the strategic leadership of the Clinical Development Team (CDT) in a matrix environment and is responsible for: the timely development and execution of the Clinical Development Plan (CDP). managing the day-to-day operations of the CDT including but not limited to meeting coordination and documentation, decision making, and stakeholder management. ensuring that the program is conducted in alignment with CSL Behring processes and abiding by GCP and ICH regulations. This position is accountable for the clinical & scientific oversight of the assigned program(s) and: ensures high quality clinical & scientific standards are met during all aspects of the program providing...

CSL The Opportunity: Reporting to the Senior Director, Head of People Analytics as the Director, People Analytics & Insights, you will lead the design and delivery of enterprise people analytics solutions that enable data-driven workforce planning, talent decisions, and organizational health monitoring across CSL. You will serve as a strategic advisor to HR leaders and business stakeholders, translating complex people data into actionable insights, executive-ready storytelling, and scalable analytics products that support business outcomes. You will will partner closely with HR Centers of Excellence (COEs), HR Business Partners (HRBPs), HR Operations, enterprise data teams, and Legal/Privacy to ensure data quality, governance, compliance, and continuous advancement of analytical maturity across the organization. This is a hybrid role, which offers a combination of an onsite and remote work schedule. #LI-hybrid The Role: People Analytics Strategy, Solution Design...

CSL As the Senior Director, Medical Affairs, you will lead the development and execution of Medical Affairs strategies and tactics to support the Specialty Disease Area (DA). You will serve as the medical and scientific expert and represent current US medical practice to internal CSL Behring stakeholders. You will have a high awareness of patient needs, current therapeutic practices and new therapeutic trends in the US market. Essential to success is an outstanding partnership with the medical field team which will report to you through a Specialty Field Medical Director; and, with Market Access, and Commercial to maximize the value proposition of the medicines in your portfolio. Externally, you will assist health care professionals and payers to optimize patient care and treatment outcomes through evidence-based decisions. You will: Lead the US Medical team (Medical directors/scientists and Field MSL Lead) for the US Disease Area Develop and execute annual US Medical...

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Lead the development, design, governance, implementation and continuous improvement of required Project Management Tools, Templates and standards for R&D to enable consistent, compliant, and high-quality project delivery across the R&D portfolio. Your Responsibilities & Accountabilities Design, develop, systematize and maintain a standardized suite of required tools, templates and supportive frameworks for R&D Project Management excellence. Primary focus is R&D Project Management within POE while serving as an extended Centre of Excellence on Project Management best practices across...

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Principal Biostatistician? The job is in our King of Prussia, PA, Waltham MA and Zurich Switzerland Office. This is a hybrid position and is onsite three days a week. You will report to the Director of Biostats. You will lead components of statistical contribution to a clinical development program. The Principal Biostatistician implements the statistical strategies for the clinical trials and regulatory submissions within the program, and is accountable for the statistical deliverables Main Responsibilities: Input to statistical strategy and ensure appropriate statistical methodologies...

CSL Primary role Summary : The PSSI Lead supports the processes associated with start-up, site monitoring, oversight and site engagement but strives to identify innovative continuous improvement opportunities with keen business analytics. They are responsible to develop and review KPI s and metrics associated with start-up, site monitoring (onsite, remote and central) and site monitoring oversight. With KPIs established, this role will need to continually monitor performance and critically assess their impact and collaborate with appropriate groups and the SMMO LT to identify trends and resolve issues and delinquencies. The PSSI Lead monitors start-up, site monitoring and oversight processes at enterprise level using dashboards and analytics; and ensures compliance through SMMO & Partner follow-up in collaboration with Clinical Compliance. The PSSI Lead represents SMMO on SOP and process reviews, determines impact and provides recommendations or process improvement...

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director of Patient Engagement? The job is in our King of Prussia, PA, Maidenhead, UK or Zurich Switzerland office. This is a hybrid position and is onsite three days a week. You will report to the Senior Director, Head of Feasibility & Patient Engagement. You will be responsible for developing and maintaining strong relationships with patient advocacy groups and collaborating with CSL Site Engagement Leads to position CSL as a preferred sponsor. This role integrates site partnership strategies (in collaboration with Site Engagement Leads) with patient-focused clinical research...

CSL The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. Provide statistical thought partnership for innovative study design and clinical development...