Clinical Solution Designer in Westminster

The Clinical Solution Designer (CSD) works closely with Project Managers and directly with customers to gather study configuration needs, which are in accordance with the clinical study protocol. Serving as a vital link between non-technical stakeholders and technical teams, the CSD conducts customer workshops to gather and translate client requirements into clear, actionable user stories and tasks. These are then presented to and refined with technical teams prior to build configuration, ensuring a seamless and accurate setup of the eCOA platform.

What will you do?

• Collaborate closely with Project Managers, technical managers, solution developers, and testers to design project deliverables of varying complexity.
• Ensure solutions align with product capabilities while meeting client needs, balancing protocol requirements and delivery team constraints.
• Lead customer workshops and proof-of-concept sessions, showcasing questionnaire designs and mapping user and study journeys that align with client protocol objectives and study requirements.
• Serve as a subject matter expert (SME) during pre‐ and post‐sales activities, reviewing study protocols to recommend optimal solutions and utilizing internal configuration tools to create prototypes for clients.
• Foster a passion for technology and innovation in clinical research, advocating for innovative user‐centric trial designs tailored to client‐specific needs.
• Effectively communicate complex technical requirements and design considerations to non‐technical stakeholders, translating their requests into actionable language for technical teams.
• Plan and prioritize user stories, managing multiple project backlogs to ensure the efficient delivery of large, multifaceted eCOA studies.
• Address complex technical design challenges by developing innovative, thoughtful solutions.
• Gain deep expertise in tools, systems, core features, and design standards to deliver high‐quality outcomes, specializing in efficient, repeatable story design processes.
• Set and champion design standards and best practices within Delivery Services, ensuring high‐quality Jira hygiene and strict adherence to requirement and story best practices, particularly for questionnaire and study design.
• Stay engaged with the evolving Life Sciences technology landscape, developing industry expertise by attending and presenting at relevant conferences to enhance knowledge and visibility.

What you need to succeed

• Bachelor's Degree in Life Sciences, Clinical Research, or Information Technology.
• Expert knowledge of clinical trial design and processes, with specialized expertise in ePRO/eCOA technologies.
• In‐depth understanding of eClinical systems used in the pharmaceutical trial industry, including IRT, RTSM, EDC, eCOA, and ePRO.
• Proficiency in Agile and other software development methodologies, with hands‐on experience applying them effectively.
• Proven experience working within cross‐functional, technical, and global teams.
• Demonstrated success managing multiple projects in fast‐paced, dynamic environments while prioritizing effectively to achieve delivery goals.
• Proven leadership ability to inspire and motivate teams in rapidly changing business conditions, maintaining a positive and proactive outlook.
• Strong analytical, technical, and problem‐solving skills.
• Exceptional interpersonal and communication skills, with the ability to build rapport and foster collaboration across diverse teams.

Nice to have

• Experience using JIRA, Slack, Miro is advantageous.

Why uMotif?

• Benefits package: Unlimited paid holiday allowance after probation, Contributory Salary Sacrifice pension, Private Health Insurance via Vitality, Simplyhealth cashback scheme, 5x salary Life Insurance, Full pay for the first 13 weeks of SMP during maternity leave, Perkbox subscription, Salary Sacrifice Cycle scheme, Remote working, Home office allowance, WFH expense contribution.

Our Company:

uMotif's mission is to put patients at the centre of research by building data capture solutions people love to use. Designed with patients for patients, the uMotif platform supports data capture for each phase of clinical research across all therapeutic areas. Over 22,000 participants use our applications to track and submit e‐consent, symptom, eCOA, ePRO, and wearable device data. With expertise in engaging patients and fast deployments, we work with ten of the top twenty global pharmaceutical companies to power large real‐world evidence (RWE) and virtual studies. Team uMotif are united in our belief that patient‐centric thinking combined with beautiful technology and effective teamwork can truly change clinical research for the better. We search for mission‐driven people who are not afraid to be challenged – who want to tackle demanding problems and embrace innovative ideas.

Our core values:

• Patients First – We care about patients and put them first; from our products to our business decisions.
• Teamwork – Through collaborating with and supporting each other, our customers, and our partners we succeed together.
• Innovation – We work innovatively to design, build, and deliver engaging technology.

uMotif is an equal opportunity employer. We positively encourage applications from suitably qualified and eligible candidates regardless of sex, race, disability, age, sexual orientation, gender reassignment, religion or belief, marital status, or pregnancy and maternity. We want everyone at uMotif to be comfortable bringing their true self to work. That means acknowledging your personality, including the quirky bits, and bringing your interests, hopes, dreams, and even fears with you is fine, even if they don't seem relevant to your work.