Associate Manager, Solutions Design
Role details
Job location
Tech stack
Job description
The Linguistic Solutions team within Instrument Services at IQVIA is currently seeking a proactive and technically skilled Associate Manager, Solutions Design to lead the design, programming, and integration of Clinical Outcome Assessments (COAs) for electronic implementation. This role focuses on the development of new COA instruments and their deployment across internal and client platforms. While direct eCOA solution delivery is not the primary focus, prior experience in eCOA implementation is highly valued., COA Instrument Design & Programming
- Design and program new COA for electronic implementation, ensuring alignment with scientific intent and digital usability.
- Translate clinical and scientific requirements into structured, platform-ready specifications, including logic, scoring, and user interface elements.
- Ensure COA content is optimized for deployment across multiple internal and client platforms.=
Platform Integration & Technical Enablement
- Configure and implement COA instruments within internal systems and client platforms, ensuring technical compatibility and performance.
- Collaborate with internal IT and platform production teams to initiate and accelerate change implementations, system updates, and platform enhancements.
- Provide technical consultation and support for platform-specific requirements, integrations, and troubleshooting.
Cross-Functional & Client Collaboration
- Partner with internal stakeholders (e.g., COA Management, Product, Engineering, Instrument Licensing & Linguistic Solutions) to align on instrument requirements and implementation strategies.
- Support client teams by advising on COA integration into their platforms and ensuring adherence to best practices and standards.
- Participate in client discussions to understand platform needs and provide technical guidance.
Sales & Business Development Support
- Collaborate with Sales and Business Development teams to promote the electronic implementation of COAs.
- Provide technical input and subject matter expertise during proposal development, client presentations, and solution scoping.
Governance, Quality, and Innovation
- Contribute to the development and maintenance of design standards, templates, and best practices for COA digitization.
- Support quality assurance activities, including peer reviews, testing, and documentation.
- Identify and implement process improvements and automation opportunities to enhance efficiency and scalability.
Requirements
Do you have experience in XML?, Do you have a Master's degree?, The ideal candidate will bring a strong foundation in clinical research, digital health technologies, and platform integration, with a collaborative mindset and the ability to drive innovation and change across cross-functional teams., * Bachelor's degree in Life Sciences, Computer Science, Engineering, or a related field (Master's degree preferred).
- 3+ years of experience in clinical research, digital health, or software/product development.
- IT consulting or project management experience.
- Experience designing or programming COA/eCOA instruments or similar digital health/registry tools.
- Familiarity with eClinical technologies (e.g., ePRO, IRT/RTSM, eConsent) and platform configuration.
- Strong understanding of data flow, logic structures, and user experience in digital health applications.
Preferred Skills
- A self-starting mind-set with excellent team-based interpersonal skills with the ability to also work independently
- Ability to work in a fast-paced environment with demonstrated skills to effectively manage multiple tasks and projects
- Results- and detail-oriented approach with excellent problem-solving skills for deliverables
- Experience collaborating with IT and platform teams to implement system changes and enhancements.
- Knowledge of metadata-driven design, XML/JSON-based configuration, or platform scripting tools.
- Broad knowledge of current technology, tools and techniques for software development.
- Understanding of clinical trial processes, regulatory standards (e.g., GCP, FDA, ICH), and COA validation principles.
- Strong communication and documentation skills, with the ability to translate technical concepts for non-technical stakeholders.
- Experience working in a matrixed or global environment.