uMotif

Clinical Solution Designer

uMotif

full-time

Posted on:

Location Type: Remote

Location: United States

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About the role

  • 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

Requirements

  • 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
Benefits
  • Unlimited Paid Time Off
  • 401(k) Retirement Plan contribution
  • Majority company funded benefits package incorporating: Health, Dental and Medex2 coverage, and a selection of Vision plans
  • Life and AD&D Insurance fully covered by uMotif
  • Remote working solutions
Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills & Tools
clinical trial designePRO technologieseCOA technologieseClinical systemsIRTRTSMEDCAgile methodologiesproject managementproblem-solving
Soft Skills
leadershipcommunicationcollaborationanalytical skillsinterpersonal skillsprioritizationinnovationteam motivationadaptabilitycustomer engagement
Certifications
Bachelor’s Degree in Life SciencesBachelor’s Degree in Clinical ResearchBachelor’s Degree in Information Technology