10 senior data analyst jobs found in Andover, MA

We are seeking a Senior Clinical Trial Manager to oversee and manage all clinical site interactions, including IRB/EC applications, contract negotiations, enrollment tracking, and issue resolution. This role involves owning and managing trial start-up, conduct, and close-out activities according to industry and corporate standards, contributing to key clinical documents, and establishing professional rapport with investigational site personnel. Responsibilities Manage all clinical site interactions including IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and clinical supply requests, and issue resolution. Own and manage all trial start-up, conduct, and close-out activities according to industry and corporate standards. Contribute to preparation of key clinical documents such as protocols, informed consent, amendments, CRFs, training materials, project plans, monitoring plans, data plans, SAPs, and reports....

Senior C++ Developer Job Description We are seeking an experienced and highly skilled Senior C++ Developer to play a key role in developing the Edge Control Server for our Building Management System (BMS) platform. In this role, you will design and build robust, high-performance applications, influence architectural decisions, mentor junior engineers, and collaborate with global teams to deliver scalable and reliable solutions in a fast-paced Agile environment. Responsibilities Lead and contribute to requirements analysis, design, and implementation. Design, build, and maintain efficient, secure, reusable, and high-quality C++ code. Drive performance optimization, debugging, and profiling. Identify architectural and design improvements and guide implementation. Ensure high standards for code quality, organization, and automation. Actively participate in code reviews and provide technical mentorship. Collaborate across global teams...

Job Title: Senior Clinical Trial ManagerJob Description We are seeking a highly experienced Senior Clinical Trial Manager to oversee all aspects of clinical trials, from start-up through close-out, ensuring compliance with industry and corporate standards. This role involves managing clinical site interactions, including IRB/EC applications, contract negotiations, and enrollment tracking, while contributing to the preparation of key clinical documents and supporting applications and technical files. Responsibilities Manage all clinical site interactions including IRB/EC applications, contract negotiations, enrollment tracking, and clinical supply requests. Own and manage trial start-up, conduct, and close-out activities according to industry and corporate standards. Contribute to the preparation of clinical documents such as protocols, informed consent forms, amendments, CRFs, training materials, project plans, monitoring plans, data plans, SAPs, and...

Lensa is a career site that helps job seekers find great jobs in the US. We are not a staffing firm or agency. Lensa does not hire directly for these jobs, but promotes jobs on LinkedIn on behalf of its direct clients, recruitment ad agencies, and marketing partners. Lensa partners with DirectEmployers to promote this job for RTX. Clicking "Apply Now" or "Read more" on Lensa redirects you to the job board/employer site. Any information collected there is subject to their terms and privacy notice. Date Posted 2026-02-25 Country United States of America Location: US-MA-ANDOVER-AN1 ~ 350 Lowell St ~ AN1 ESSEX BLDG Position Role Type Onsite U.S. Citizen, U.S. Person, Or Immigration Status Requirements The ability to obtain and maintain a U.S. government issued security clearance is required.? U.S. citizenship is required, as only U.S. citizens are eligible for a security clearance Security Clearance Type Secret - Current Security Clearance Status Active and...

Senior C++ Developer Job Description We are seeking an experienced and highly skilled Senior C++ Developer to play a key role in developing the Edge Control Server for our Building Management System (BMS) platform. In this role, you will design and build robust, high-performance applications, influence architectural decisions, mentor junior engineers, and collaborate with global teams to deliver scalable and reliable solutions in a fast-paced Agile environment. Responsibilities Lead and contribute to requirements analysis, design, and implementation. Design, build, and maintain efficient, secure, reusable, and high-quality C++ code. Drive performance optimization, debugging, and profiling. Identify architectural and design improvements and guide implementation. Ensure high standards for code quality, organization, and automation. Actively participate in code reviews and provide technical mentorship. Collaborate across global teams...

Overview: At PNNL, our core capabilities are divided among major departments that we refer to as Directorates within the Lab, focused on a specific area of scientific research or other function, with its own leadership team and dedicated budget. Our Science & Technology directorates include National Security, Earth and Biological Sciences, Physical and Computational Sciences, and Energy and Environment. In addition, we have an Environmental Molecular Sciences Laboratory, a Department of Energy, Office of Science user facility housed on the PNNL campus. The Energy and Environment Directorate (EED) delivers science and technology solutions for the nation’s biggest energy and environmental challenges. Our more than 1,700 staff support the Department of Energy (DOE), delivering on key DOE mission areas including: modernizing our nation’s power grid to maintain a reliable, affordable, secure, and resilient electricity delivery infrastructure; research, development,...

We are hiring for entry level, mid level, and expert level Software Engineers! See below for details and apply to learn more! Responsibilities Participate in requirements analysis and design discussions. Develop, enhance, and maintain applications on the Edge Control platform. Write clean, efficient, testable, and maintainable code. Debug issues and assist with performance and stability improvements. Collaborate with senior engineers to learn design patterns and best practices. Contribute to code reviews and Agile ceremonies. Support defect resolution and incremental improvements to existing systems. Essential Skills Entry-Mid level: 1-3 years of hands-on experience in software development (with C++) or strong academic/project experience. Expert level: 5+ years of professional C++ development experience. Solid understanding of object-oriented programming principles. Familiarity with writing modular,...

We are hiring for entry level, mid level, and expert level Software Engineers! See below for details and apply to learn more! Responsibilities Participate in requirements analysis and design discussions. Develop, enhance, and maintain applications on the Edge Control platform. Write clean, efficient, testable, and maintainable code. Debug issues and assist with performance and stability improvements. Collaborate with senior engineers to learn design patterns and best practices. Contribute to code reviews and Agile ceremonies. Support defect resolution and incremental improvements to existing systems. Essential Skills Entry-Mid level: 1-3 years of hands-on experience in software development (with C++) or strong academic/project experience. Expert level: 5+ years of professional C++ development experience. Solid understanding of object-oriented programming principles. Familiarity with writing modular,...

Job Title: Senior Clinical Trial Manager Job Description We are seeking a Senior Clinical Trial Manager to oversee and manage all clinical site interactions, including IRB/EC applications, contract negotiations, enrollment tracking, and issue resolution. This role involves owning and managing trial start-up, conduct, and close-out activities according to industry and corporate standards, contributing to key clinical documents, and establishing professional rapport with investigational site personnel. Responsibilities Manage all clinical site interactions including IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and clinical supply requests, and issue resolution. Own and manage all trial start-up, conduct, and close-out activities according to industry and corporate standards. Contribute to preparation of key clinical documents such as protocols, informed consent, amendments, CRFs, training materials, project plans,...

Job Title: Senior Clinical Trial Manager Job Description We are seeking a Senior Clinical Trial Manager to oversee and manage all clinical site interactions, including IRB/EC applications, contract negotiations, enrollment tracking, and issue resolution. This role involves owning and managing trial start-up, conduct, and close-out activities according to industry and corporate standards, contributing to key clinical documents, and establishing professional rapport with investigational site personnel. Responsibilities Manage all clinical site interactions including IRB/EC applications, contract negotiations, enrollment tracking, clinical trial material and clinical supply requests, and issue resolution. Own and manage all trial start-up, conduct, and close-out activities according to industry and corporate standards. Contribute to preparation of key clinical documents such as protocols, informed consent, amendments, CRFs, training materials, project plans,...