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Location
In office (Manila)
Seniority
Junior · 2+ years exp
Visa
Sponsors visas in United States, United Kingdom; no register of this country names it

Confirmed on the employer's own hiring board on Nov 10, 2026. First seen by Alion on Nov 5, 2026. Signant Health scores A on the Alion truth index.

Overview
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Signant Health is a clinical trial technology and services company headquartered in Blue Bell, Pennsylvania, providing electronic clinical outcome assessments, EDC, randomization and trial supply management, eConsent and clinical data analytics to drug sponsors and CROs. Its platforms and scientific services support studies in more than 90 countries and have contributed to hundreds of new drug approvals, with operations teams in India, the Philippines, Romania, Chile and Mexico. The company hires help desk agents including Japanese speakers, clinical support specialists, data management leads, solution and operations software engineers, project and product managers and sales staff.

About Signant Health

At Signant Health, we help bring life-changing treatments to patients faster. We are a global evidence generation company that supports clinical trials with smart technology, scientific expertise, and hands-on operational support — so better data leads to better decisions in healthcare. We embrace AI and advanced technologies to enhance every aspect of what we do, from data analysis to operational efficiency.

Our teams work at the intersection of science, technology, and patient experience, delivering digital solutions powered by AI innovation that make clinical trials more efficient, more accurate, and more accessible around the world. Trusted by leading pharmaceutical companies and CROs, our platforms and services support studies across more than 90 countries and have contributed to hundreds of new drug approvals.

If you are motivated by meaningful work, global impact, and innovation in clinical research and digital health — including the opportunity to work with cutting-edge AI technologies — you will find purpose and opportunity at Signant Health.

Location: Metro Manila

Work mode: Remote

Shift Timings: 5:00 PM - 2:00 AM

About the Role

Solution Engineer is responsible for working with Sponsors/Customers, Clinical, Global Project Management (GPM), Data Management and across the matrixed Global Technical Delivery (GTD) to design solutions for clinical trials utilizing Signant Health’s product portfolio. They analyse study protocol requirements and define solutions considering scientific guidance, electronic clinical outcome assessment (eCOA) best practices and Signant’s products and standards. They play a key role in ensuring the project meets the study needs and is feasible to implement, based upon the capabilities and limitations of the product, in the quoted timelines and budget. They are responsible for understanding business needs and translating them into system requirements.  They may assist with the development and documentation of processes and procedures.

KEY ACCOUNTABILITIES - Function

Collaborate with other Solution Engineers, and others as determined, to ensure questionnaires, clinical trial protocol, and overall design requirements are understood and can be implemented as well as analyse the protocol/scope to collate the design requirements for simple to moderate complexity projects.

Produce functional requirements documentation based upon design requirements shared by Senior and/or Lead Solution Engineer, as necessary.

Utilize all available tools and information sources to understand requirements, including interviews/meetings, document analysis, use cases and workflow analysis.

Update and mange requirements/specifications as needed throughout the software development lifecycle. Follows defined validation processes and produces validated documents for all questionnaires.

Evaluate information gathered from multiple sources, work with stakeholders to reconcile conflicting information, identify/evaluate potential risks and translate abstract or high-level requirements into useful/actionable implementation.

Ensures best practices and standards are followed in every implementation.

Liaise with Localization to facilitate the development of translated versions of the master questionnaire.

May be responsible for application configuration.

They provide support for SDLC and validation documents as well as facilitate the review and approval of all documents.

Creation of Data Extract requirements and associated deliverables for project.

Assist in posting of data extract deliverables for projects. 

Creation of Custom Report requirements and deliverables

KNOWLEDGE, SKILLS & ATTRIBUTESEssential:

Bachelor’s degree or equivalent years of professional role.

2-3 years’ experience functioning as Business Analyst or similar role.

In depth experience with Software Development Life Cycle (SDLC) implementation

Gathering information from a wide variety of sources and subsequently crafting it into effective and audience-appropriate technical and non-technical documentation.

Excellent analytical and problem-solving skills and a desire to solve problems.

Ability to resolve conflicts between people and competing goals and interests.

Desire for developing one’s own skills:  technical, clinical, and interpersonal.

Have good communication abilities via writing, quality documentation and presenting in meetings. Delivers information effectively and timely. Uses interpersonal skills to build and develop relationships with internal and external team members.  

Needs to be an effective, positive team player, and a self-starter, with moderate level of guidance and direction.

Must have very strong skills with Microsoft Office application to include the following: Word, Excel, Visio and PowerPoint.

Proficiency in HTML and CSS for questionnaire configuration and system customization purposes.

Desirable:

Software development background/experience

User experience/interface degree/experience

Familiarity with GCP and 21 CFR Part 11 is a plus

Familiarity with SQL Queries is a plus.

 

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