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At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.

Senior Integrations Engineer

Job Summary: We are looking for a certified professional with extensive experience in IT and specialized knowledge in eTMF and CTMS specific software platform. The ideal candidate will have a strong background in system support, data uploads, and compliance deliverables within the life sciences industry.

Key Responsibilities:

• Utilize expertise in the software platform, including data loading tools, comparison tools, audit trails, API tools, workflows, file management, collaborative authoring, configuration reports, access control, and user security roles.
• Assist business users with application features and data uploads.
• Provide hands-on system support, handle support tickets, and resolve issues efficiently.
• Create and manage compliance deliverables such as test plans, test scripts, risk assessment documents, traceability matrices, and other compliance-related documents.
• Specialize in electronic trial master file (eTMF) and clinical trial management system (CTMS), support ticket systems, and other project management tools.
• Collaborate with the product team to prioritize, plan, and implement enhancements to the CTMS.
• Lead efforts to configure the CTMS to adapt to evolving clinical trial requirements, ensuring seamless integration and support from vendors.
• Define strategies for configuring the CTMS to meet trial needs and continuous improvement initiatives, coordinating with the Product Owner (PO) to decide on solutions and process improvements.
• Co-define the priority of scripts to be automated first to ensure full coverage of system changes.
• Develop and deploy configurations in the system, supporting end-to-end documentation and validation of system change requests.
• Address production issues based on severity as determined by the business.
• Collaborate with Global Clinical Operations (GCO) and work closely with divisional clinical Subject Matter Experts (SMEs).

Qualifications:

• Veeva certification.
• 10+ years of IT experience
• 5+ years in the Veeva platform.
• Proven experience with data loading tools, comparison tools, audit trails, API tools, workflows, file management, collaborative authoring, configuration reports, access control, and user security roles.
• Strong understanding of compliance deliverables and requirements.
• Proficiency in support ticket systems and other project management tools.
• Excellent problem-solving skills and attention to detail.
• Strong communication and interpersonal skills.

Preferred Qualifications:

• Experience in the life sciences industry.
• Familiarity with eTMF and CTMS.
• Veeva Vault Development Cloud

Requisition ID: 590560

As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!