
201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
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201 - 500 employees
💊 Pharmaceuticals
🏥 Healthcare
💼 Consulting
Pharmaceuticals • Healthcare • Consulting
Innovaderm Research Inc. is a Contract Research Organization (CRO) specialized in dermatology, providing scientific guidance and conducting Phase I to IV clinical trials in the field. With a strong presence in North America and Europe, Innovaderm offers a comprehensive range of services including study design, regulatory consulting, project management, patient recruitment, and data management, ensuring high-quality research outcomes and customer satisfaction since 2000.
• Develop and update risk-based monitoring strategies tailored to project needs • Collaborate with cross-functional teams to identify and mitigate risks associated with complex indications • Coordinate with the central monitor team and verify work when required • Provide budget recommendations and change orders • Draft initial risk assessments and support finalization of Risk Assessment and Categorization Tools (RACT) • Guide Project Managers in transferring identified risks to appropriate tracking systems and ensure ongoing reviews • Advise on functional plans to mitigate risks • Conduct remote data reviews and centralized statistical monitoring using available tools • Identify risks to data quality and integrity • Facilitate internal and sponsor reviews of findings • Seek cross-functional support for complex risks and mitigations • Deliver initial and ongoing training for study teams on risk assessment, centralized monitoring, and risk-based monitoring strategies • Escalate risks, at-risk deliverables, and scope changes to the Project Manager • Provide strategic input on risk characterization and reporting to leadership • Perform additional responsibilities as assigned when qualified and adequately trained
• Bachelor’s degree in a field relevant to clinical research • Experience in a CRO or pharma industry • Minimum of 3 years in risk management within a clinical research setting • Minimum 5 years of experience across clinical monitoring, data management, and drug safety • Expertise in Good Clinical Practice/ICH E6 (R3) Guidelines and other regulatory requirements • Proficiency in Risk-Based Monitoring strategies, processes, and tools • Mastery of MS Excel, including sorting, filtering, and pivot tables • Advanced skills in analytical data visualization tools • Knowledge of Lean Six Sigma and web-based RACT tools • Strong analytical and statistical understanding • Excellent communication, negotiation, and leadership skills • Ability to anticipate critical issues and develop proactive contingency plans • Skilled in project workflows and cross-functional collaboration • Training, mentoring, and organizational capabilities • High level of autonomy • Fluent in English, with excellent oral and written communication • Ability to communicate clearly and effectively at all organizational levels and with external customers • Fast learner able to understand new concepts quickly • Prioritization skills and ability to plan, monitor, and manage workload in response to changing project demands • Excellent understanding of project protocols and documentation, including centralized monitoring and risk-based monitoring • Broad working knowledge of clinical trial roles, functions, and processes • Effective time management while working with multiple functions and requirements • Experience using trial management or data management systems • Good knowledge of good clinical practices and applicable Health Canada and FDA regulations/guidelines • Must be legally able to work in the Philippines
• Flexible work schedule • Permanent full-time position • Ongoing learning and development • Attractive advancement opportunities • Recruitment and selection accommodations for applicants with disabilities, upon request
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