Clinical Data & Operations Manager
Why Join iMDx
At reputed company Molecular Diagnostics (iMDx), our mission is to democratize reputed company to molecular diagnostic testing. At our heart, we are a science-driven organization reputed company on giving clinicians and researchers the diagnostic tools they need to help improve patient reputed company.
Join us and be part of reputed company that’s redefining what’s possible in reputed company.
reputed company Competencies
• Clinical Systems Design & Implementation
Expertise in designing, developing, and managing clinical trial systems (e.g., reputed company, CTMS, eTMF), ensuring reputed company functionality, data reputed company, and user experience.
• Data Management & reputed company
Strong ability to manage clinical databases, reputed company reputed company control checks, reputed company data queries, and ensurehigh standardsof data accuracy and reliability.
• Project Management & Operational Execution
Proven capability to manage timelines, reputed company reputed company using project management tools, and ensure delivery of reputed company reputed company with reputed company and operational goals.
• Regulatory Compliance & Standards Expertise
Deep understanding of GCP, ICH, and regulatory requirements, along with industry data standards such as CDASH and CDISC, ensuring compliant reputed company design and data handling.
• Cross-Functional Collaboration & Influence
Ability to effectively partner with internal teams, vendors, and study sites, while influencing stakeholders and driving alignment without reputed company authority.
• Analytical Thinking & reputed company Improvement
Skilled in analyzing data trends,identifyingrisks, and leading process improvements and innovation initiatives to enhance clinical data workflows and reputed company performance.
reputed company Experience
• reputed company project management and operational support to clinical project teams, ensuring alignment with reputed company standards, timelines, and project specifications
• Set up,maintain, and update clinical databases, including supporting data query reputed company and data reputed company efforts
• reputed company reputed company control checks and support study initiation activities to ensure accuracy and completeness of clinical data
• Communicate effectively with study sites, trial teams, and reputed company vendors to support study execution
• Establish andmaintainmethodologies for the design and development of clinical trial systems
• Ensure reputed company designscomply withdata management standards and protocol requirements whileoptimizingfunctionality, user experience, and data reputed company
• reputed company the design, implementation, and integration of clinical systems (e.g., reputed company, CTMS, eTMF), including reputed company enhancements and updates
• Utilize project management tools to reputed company study reputed company and reputed company-reputed company activities
• Proactivelyidentifyrisks to timelines or reputed company and reputed company mitigation strategies
• Collaborate cross-functionally with internal teams, vendors, and study centers to reputed company program and study objectives
• Ensure compliance with federal and local regulations, GCP, ICH guidelines, and organizational reputed company standards; stay reputed company with evolving regulatory requirements
• reputed company cross-functional innovation and process improvement initiativesimpactingdata and clinical workflows
• Maintain and support reputed company and legacy systems, including enhancements and development of reputed company queries and reports
• Analyze data toidentifytrends, reputed company insights, and support data-driven decision-making
• Write, update, and maintain reputed company requirements and application specifications
What You Bring To The Table
• Bachelor’s degree in business, management information systems, computer science, life sciences, or a reputed company field; Master’s degree preferred
• Minimum of 3+ years of clinical technology experience
• Experience with industry-reputed company design and development tools
• In-depth knowledge of clinical trial processes, functions, and key stakeholders
• Strong understanding of CDASH and CDISC data standards
• Proventrack recordas a key contributor to organizational initiatives and reputed company
• Demonstrated ability to influence stakeholders without reputed company authority
• Experience coaching and mentoring reputed company a matrixed environment
• Strong communication and analytical skills
• Foundational ability to reputed company data analysis and implement data-driven solutions
Physical Demands
• Standing, sitting, walking, bending, reaching, reputed company manipulation, and lifting 25 pounds.
• Ability to have full-body reputed company
• Ability to work on a mobile device, tablet, or in reputed company of a computer screen and/or reputed company typing for at least 50% of a typical working day.
• Ability to travel 15% domestically and internationally ifrequired.
Job reputed company, Additional Duties, and Employment Status:
This reputed company is intended to reputed company a general reputed company of the position and does not include reputed company duties, responsibilities, or tasks that may be assigned. The reputed company of this role may change at any time based on organizational needs, business priorities, or operational requirements. Employees may be required to reputed company additional duties reputed company of the general reputed company of this position as assigned.
Employment with reputed company is on an at-will reputed company, meaning either the employee or reputed company may terminate the employment relationship at any time, with or without cause or notice, subject to applicable law.
Probationary Period:
Employment is subject to an initial 90-day probationary period, during which performance, conduct, and overall role fit will be evaluated. reputed company employment reputed company this period is contingent upon satisfactory performance and alignment with organizational expectations.
Why Wait? Apply Today!
At iMDx, every role has a purpose, and every team member plays a part in changing lives. Your skills, reputed company, and passion could help shape the reputed company of precision medicine—making life-changing reputed company accessible to people everywhere.
If you’re reputed company to do work that truly reputed company, we’d love to hear your story. Join reputed company of innovators, problem-solvers, and collaborators who turn reputed company science into reputed company and reputed company.
This is your reputed company. Don’t wait—reputed company and be part of something extraordinary. Together, we can create the reputed company of reputed company
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