Associate eCOA Manager

đź•’ vor 9 Tagen

🇬🇧 Vereinigtes Königreich – Remote

⏰ Vollzeit

🟢 Junior

🟡 Mittelstufe

đź‘” Manager

🇬🇧 UK-Skilled-Worker-Visum-Sponsor

infoinfo

đź‘» Geisterscore 20%

infoinfo

🗣️🇺🇸🇬🇧 Englisch erforderlich

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Logo of Worldwide Clinical Trials

Worldwide Clinical Trials

1001 - 5000 Mitarbeiter

🏥 Gesundheitswesen

đź’Ľ Beratung

📦 Logistik

Healthcare • Consulting • Logistics

Worldwide Clinical Trials ist eine globale Auftragsforschungsorganisation (CRO) und bietet umfassende Dienstleistungen für klinische Studien. Das Unternehmen ist auf die Unterstützung von Studien in verschiedenen Therapiegebieten wie Onkologie, Kardiologie und seltenen Erkrankungen spezialisiert. Mit über 30 Jahren Erfahrung legt Worldwide Clinical Trials Wert auf persönliche Betreuung und maßgeschneiderte Lösungen über den gesamten Lebenszyklus der Arzneimittelentwicklung hinweg. Zum Serviceportfolio zählen unter anderem klinisches Monitoring, Data Management, Patient Recruitment sowie Regulatory Consulting – für Präzision und individuelle Aufmerksamkeit in jeder klinischen Studie.

Beschreibung

• Provide project management oversight from maintenance through eCOA decommissioning • Oversee and maintain accountability for deliverables, timelines, and completion of work according to Worldwide SOP standards • Review and identify study trends and proactively work with eCOA vendors and study teams to address study-specific requirements • Communicate applicable eCOA project activities to internal and sponsor study teams • Serve as the escalation point of contact for eCOA assigned study-related project issues • Coordinate timely delivery of eCOA project communications, including study status reports, meeting agendas, minutes, and project call scheduling • Provide overall eCOA study design review and approve User Requirements Specifications (URS) for post-go-live Change in Scope • Prepare, review, and approve site and support materials and helpdesk documentation when required • Perform financial review and budget management, including review of Change Orders

🎯 Anforderungen

• Ability to communicate concisely and effectively in both written and spoken English • Proficient client-facing skills • Self-motivated and able to contribute positively to a team environment • Ability to prioritize and handle multiple projects simultaneously • Flexible, able to use sound independent judgment, and take initiative • Ability to make effective decisions in a fast-paced, highly dynamic environment • Ability to adapt to new technologies, concepts, and processes • Ability to make improvements and solve problems • Highly organized, detail- and service-oriented • Excellent project management skills • Educated to degree level in a relevant discipline or able to demonstrate equivalent experience • Minimum 1 year of experience working in eCOA and clinical trials • Minimum 1 year of experience in project management • Demonstrable knowledge of operational aspects regarding Phase I-IV clinical research trials • Knowledge of the Software Development Life Cycle (SDLC) • Familiarity with eCOA topics, including eCOA designs and scales • Contract Research Organization (CRO) or pharmaceutical experience required • Fluency in English required to write, speak, and understand English for day-to-day business • May require domestic and international travel • May require flexible time management to respond to stakeholders in different time zones

🏖️ Vorteile

• Mentorship and training • Opportunities for internal promotions and growth • Diverse and inclusive work environment • Remote work arrangement • Equal employment opportunities

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