eCOA & RTSM Application Specialist

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🔥 0 minutes ago

🇿🇦 South Africa – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 12%

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Innovaderm Research Inc.

WebsiteLinkedInAll Job Openings

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.

📋 Description

• Support the design, deployment, configuration, and oversight of eCOA solutions, including ePRO, eConsent, and other patient-centric electronic data capture tools, and RTSM across global clinical studies. • Act as an eCOA and RTSM subject matter expert during study start-up, maintenance, and close-out. • Define functional requirements and participate in solution design and configuration. • Draft and maintain system specifications, user requirements, edit checks, notifications, and reporting requirements. • Assist with eCOA-related Case Report Form (CRF) design. • Create User Acceptance Testing (UAT) scripts and coordinate or perform system validation testing. • Validate eCOA logic, rules, and study calculations against protocol requirements. • Support CDISC-compliant data mapping and collaborate with Clinical Data Standards teams. • Contribute to data cleaning strategies and review data management plans and edit check specifications. • Prepare study-specific training materials and support training delivery. • Lead or participate in internal and sponsor meetings regarding system setup, changes, and issue management. • Document system configuration and file eCOA and RTSM deliverables in the Trial Master File (TMF). • Manage updates, amendments, and change requests throughout the study lifecycle. • Troubleshoot issues, escalate risks, and ensure timely resolution with vendors and project teams. • Ensure compliance with ICH-GCP, FDA, EMA, and other relevant regulatory standards. • Contribute to SOPs, work instructions, process improvement initiatives, templates, and eCOA and RTSM standards. • Support continuous improvement, training, and knowledge sharing within Clinical Data Management. • Stay current on emerging eCOA and RTSM technologies, regulatory trends, and best practices. • Support vendor evaluation, standardization, and relationship management when applicable. • Act as a resource for cross-functional teams regarding eCOA and RTSM processes, timelines, and risks. • May be assigned other responsibilities when appropriately experienced, qualified, and/or trained.

🎯 Requirements

• Bachelor’s degree in Life Sciences, Computer Science, Health Sciences, or related field. • 3–5 years of experience in eCOA, EDC, IRT, or eClinical solutions within a CRO, pharma, or health-technology environment. • Strong knowledge of eCOA systems and patient-reported outcomes (ePRO). • Solid understanding of clinical trial processes and data management principles; CDISC knowledge is an asset. • Experience with system configuration, UAT, edit checks, and validation activities. • Ability to collaborate in cross-functional settings and manage multiple priorities. • Analytical mindset with strong problem-solving skills. • Excellent written and verbal communication skills. • Global trial experience and knowledge of regulatory expectations (FDA, EMA, GDPR, HIPAA). • Attention to quality and data integrity. • Technical curiosity and digital mindset. • Problem solving and escalation awareness. • Stakeholder communication and collaboration. • Organization, accountability, and autonomy. • Good knowledge of good clinical practices and applicable Health Canada and Food and Drug Administration (FDA) regulations/guidelines. • Must be legally authorized to work in South Africa.

🏖️ Benefits

• 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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