Location : Remote
- Salt Lake City, UT (PST preferred)
Employment Type : Contingent Worker (Contract, W2)
Contract Length : 12 months (possible extension)
Compensation : $65 / $84 per hour (based on experience)
Summary of the Role
Join a cross-functional team to support the implementation and maintenance of Interactive Response Technology (IRT) solutions for clinical trials at a large biotech pharmaceutical leader. You will provide technical oversight to ensure that IRT systems align with study protocols, industry regulations, and company policies. The role requires strong collaboration with internal stakeholders and external technology suppliers. Serve as the subject matter expert and champion for IRT system strategy and delivery.
Key Responsibilities
Serve as the champion and consultant for efficient and effective IRT system design per study protocolLead and facilitate system requirements gathering meetings with clinical study teams and IRT supplier contactsDesign and oversee development of study-specific IRT technical documentationDocument issues and risks, and implement mitigation plans in partnership with study team and technology supplier project managersIdentify and track study-related technical issues through to resolutionClosely manage project timelines and related activitiesNegotiate with external vendors and manage project stakeholdersSupport IRT users internally and externally with a high level of serviceRequired Experience & Skills
Experience in designing or maintaining IRT (Interactive Response Technology) systems for clinical trialsStrong understanding of systems integration as it relates to IRT systemsExperience with IRT / RTSM platformsPharma, biotech, or IRT supplier experience requiredProject and people management skillsFamiliarity with regulated environments and documentation requirementsClear communication and collaborative approachAbility to lead projects under tight timelinesPreferred Qualifications
5+ years focused on IRT experienceBachelor's degree in life science, computer science, engineering, business, or a related field4+ years of experience in clinical operations, clinical supply chain, or clinical systems managementExperience implementing clinical systems such as IRT and eCOAWorking knowledge of Good Clinical Practices and FDA regulationsDetail-oriented with strong multi-project management skillsExcellent documentation, communication, and facilitation abilitiesVendor management experienceStrong time management and organization in deadline-driven settingsProblem-solving, judgment, and decision-making skillsAbility to work well independently and within a team environmentTop 3 Must Have Skills
Technical expertise in IRT systemsProject and stakeholder managementManaging documentation in a regulated environmentDay-to-Day Responsibilities
Act as primary consultant for IRT design decisions per clinical protocolFacilitate requirements meetings with study teams and suppliersOversee development of technical documents for IRT studiesEscalate and manage technical issues and risksTrack and document issue resolution with diverse stakeholdersDrive timelines and ensure all project activities are coordinatedBasic Qualifications
Doctorate DegreeMaster's Degree and 2 years of IRT experienceBachelor's Degree and 4-5 years of IRT experience, clinical experienceAssociate's Degree and 10 years of IRT experienceHigh school diploma / GED and 12 years of IRT experience"This posting is for Contingent Worker, not an FTE"
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