Sr. Principal Engineer, Clinical Data Platforms

Job Description

General Summary:

We are seeking a unique leader with a passion for data and technology responsible for leading and managing our growing delivery & operations team that manage and enable Vertexs Clinical Data Standards & Electronic Data Capture (EDC) solutions enterprise wide. As part of the Data & Software Engineering Team (DSE) you will enable our Clinical Data Management & Study Teams with accurate and secure information to analyze trials using our centralized platform.

Vertex Pharmaceuticals is in a transformational period where we are accelerating our capabilities technologies and data to augment our scientific mission enable Vertex to grow in scale and continue to be on the forefront of science medicine and technology. As part of this effort it is critical that users have data at their fingertips with a strong platform team to build and enable additional value.

The Associate Director Clinical Data Platform will be a key member of the Data Platforms team driving forward delivery & operations teams and maximizing business value for Vertex. You will be responsible for managing a team of operations leads engineers and consultants who build enhance and manage critical Clinical data solutions across the enterprise. You will engage with IT teams to improve our existing data solutions and drive increased value with our Clinical Data Standards Platform (CDSP) and our EDC capabilities. You will work in partnership with the Director Data Platforms to architect sound solutions secure data deliver continuous value standardize our solutions and advance our data platform. You will play a key role in the Vertex story.

Key Responsibilities:

• Delivery management Estimate architect and execute on the delivery of critical clinical data solutions across the enterprise in partnership with the DSE leadership team
• Operations Management Lead a comprehensive global team of engineers and consultant teams to deliver value and manage Vertexs CDSP and EDC technologies
• Business Engagement partner with and enable the Clinical Data Management Quality Regulatory & Study execution teams to deliver on prioritized outcomes
• Application & solution management Own operate and manage GCP data and analytics solutions in alignment with SOPs and industry best practices
• Team management - Lead and mentor a high performing team of employees and contractors to deliver predictable value with quality and agility
• Technology champion Advocate for automation security compliance and standards across the Clinical Data Management space
• Innovation champion - Advocate for process enhancements and opportunities to improve our data & analytics capabilities with a focus on modern data engineering capabilities and approaches

Qualifications:

• Successful track record working with Clinical Data Platforms & Clinical Trial Data
• Successful track record managing an integrated vendor team supporting an organization 24/7/365
• Demonstrated experience working with GxP solutions in the Clinical Trials environment
• Experience in delivery in agile environments (5 years)
• Demonstrated ability to work independently and manage multiple projects that require collaboration across clinical areas
• Skillful collaborative team player able to develop rapport and credibility with stakeholders
• Demonstrated ability and willingness to teach engage and support others as they learn new technologies and concepts
• Enthusiasm for and the ability to quickly learn new technologies and tackle difficult problems
• An understanding of enterprise software development tools and methodologies
• Strong presentation verbal and written communication skills
• Strong understanding of FDA ICH & CDISC regulations and industry standards
• Strong understanding of Clinical platforms including Veeva CDMS and Elluminate and the management of a technology ecosystem
• High level of comfort sourcing manipulating and visualizing clinical data and providing contextualized data to business teams
• Demonstrated understanding and experience with authoring developing and maintaining SOPs for Clinical applications

Education and Experience:

• Bachelors degree in technology discipline or equivalent
• Typically requires 8 years relevant business systems in the Life Sciences industry or the equivalent combination of education and experience

Pay Range:

Disclosure Statement:

Flex Designation:

Flex Eligibility Status:

In this Hybrid-Eligible role you can choose to be designated as:
1. Hybrid: work remotely up to two days per week; or select
2. On-Site: work five days per week on-site with ad hoc flexibility.

Note: The Flex status for this position is subject to Vertexs Policy on Flex @ Vertex Program and may be changed at any time.

Company Information

Vertex is a global biotechnology company that invests in scientific innovation.

Vertex is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a persons race color sex gender identity or expression age religion national origin ancestry ethnicity disability veteran status genetic information sexual orientation marital status or any characteristic protected under applicable law. Vertex is an E-Verify Employer in the United States. Vertex will make reasonable accommodations for qualified individuals with known disabilities in accordance with applicable law.

Any applicant requiring an accommodation in connection with the hiring process and/or to perform the essential functions of the position for which the applicant has applied should make a request to the recruiter or hiring manager or contact Talent Acquisition at