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Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates extensive knowledge of clinical trial processes, ICH-GCP regulations, and global drug development, while effectively collaborating with multidisciplinary teams to deliver high-quality solutions. Proven ability to analyze clinical operations and provide insights for product improvements and training within a SaaS environment.
Highest-signal resume keywords
Clinical Operations ExperienceKnowledge of ICH-GCP RegulationsClinical Research MethodologiesStrong Critical Thinking SkillsFluency in Required Language
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesGlobal Drug DevelopmentClinical Research MethodologiesRisk AnalysisSaaS SolutionsProtocol ReviewData AnalysisTemplate MaintenanceTraining and MentoringOperational Documentation
Soft Skills
Strong Communication SkillsProblem-Solving SkillsTime Management SkillsAdaptabilityInterpersonal Skills
Industry Keywords
Clinical ResearchCROTherapeutic AreasStudy CoordinatorResearch NurseCRAOperational OversightQuality AssuranceRegulatory ComplianceIreland Work Permit
About the role
Key responsibilities & impact- Act as a clinical trial advisor and subject matter expert, providing clinical oversight on a multidisciplinary team to ensure timely delivery of high-quality solutions
- Review study protocols and documents to identify vulnerabilities and operationally important areas, and customize the platform for individual study requirements
- Review projects from an end-user perspective for quality, accuracy and relevance before client deployment
- Review and analyze study-level risk registers/RACTs to define Engage messaging campaigns and other Teckro platform use cases
- Present findings and suggestions to client study teams with support from the Project Manager and/or Program Lead/Director
- Monitor and analyze platform searches, identify trends and unanticipated key variables, and provide data to development teams for product improvements
- Act as a clinical trials resource for the Product team, assisting with testing new functions and providing insight into clinical research professionals’ day-to-day work
- Maintain and improve in-house templates, SOPs and guides
- Assist with training, induction and upskilling of CRS team members, including mentoring, shadowing and Level 3 duty training
- Undertake other duties aligned with the role and business requirements
- Contribute ideas for innovation and product, quality and process improvements
Requirements
What you’ll need- Minimum 3 years of clinical operations/clinical research experience within a hospital or CRO setting (study coordinator, research nurse, CRA/study monitor)
- In-depth knowledge of global drug development, clinical trial processes, ICH-GCP, regulations and documentation
- Broad clinical research experience from working within a variety of therapeutic areas preferred
- Keen interest in technology solutions and Software as a Service (SaaS)
- Experience with clinical operations/industry-related technology solutions and ability to learn new software preferred
- Strong critical thinking and problem-solving skills
- Strong multi-tasking and time management skills, including ability to effectively prioritize tasks based on timelines and demands
- Ability to work independently and in a team-oriented, collaborative environment with minimal or no supervision
- Strong interpersonal, verbal and written communication skills
- Results and performance driven
- Adaptable and flexible
- Proven spoken and written fluency in the specific language required for assigned duties
- Degree in biological science, nursing, pharmacy or another health-related discipline
- Proven competencies with clinical research methodologies and operational day-to-day activities
- Must currently be based in Ireland and already hold the necessary legal permissions to work in Ireland; work permit sponsorship unavailable
Benefits
Comp & perks- 25 days holidays, entitlement increases with length of service
- Pension
- Healthcare
- Life Insurance
- Paid Paternity leave scheme
- Bike to Work/ Tax Saver Scheme
- Gym/Wellness Allowance
- Sports and Social Club
- Flexible start/end times