eCOA & RTSM Application Specialist

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🔥 0 minutes ago

🇦🇷 Argentina – 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 patient-centric electronic data capture tools • Support Randomization and Trial Supply Management (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 plans such as DMPs and edit-check specifications • Prepare study-specific training materials and support training delivery • Lead or participate in meetings with internal teams, sponsors, and vendors 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 improvements, templates, and eCOA/RTSM standards • Support continuous improvement, training, and knowledge sharing within Clinical Data Management • Monitor emerging eCOA and RTSM technologies, regulatory trends, and best practices • Support vendor evaluation, standardization, and relationship management when applicable • Advise cross-functional teams on eCOA and RTSM processes, timelines, and risks • Perform other assigned responsibilities when qualified and adequately 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 FDA regulations/guidelines • Must be legally authorized to work in Argentina

🏖️ 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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