Clinical Community Analyst

atICON plcRemotePL flagPolandFull-timeCommunity ManagerMid-levelSenior

Posted 10 hours ago

This is a fully remote position, open to applicants in Poland.

πŸ“‹ Description

β€’ Oversee investigator portals from the initiation of studies through to their conclusion and subsequent archiving.

β€’ Collaborate with study teams to create and implement strategies for site engagement and communication.

β€’ Develop, maintain, and publish content for the portal, including news updates, communications, surveys, forms, dashboards, and study resources.

β€’ Manage portal launches and ongoing activities in coordination with study teams and external vendors.

β€’ Assist in user management for the portal and provide business support to stakeholders.

β€’ Lead and conduct meetings with study teams regarding portal planning, implementation, and ongoing study operations.

β€’ Track portal activity and engagement, identifying opportunities to enhance the site experience.

β€’ Investigate, monitor, and resolve issues related to the portal, escalating as necessary.

β€’ Contribute to process enhancements, training initiatives, operational documentation, and the development of best practices.

β€’ Provide support for wider site engagement initiatives and technology-related projects as needed.


⛳️ Requirements

β€’ A degree in Life Sciences, Health Sciences, or equivalent relevant experience.

β€’ Experience in clinical trials or clinical research environments.

β€’ Familiarity with investigator portals or similar clinical technology platforms that aid study sites and investigators.

β€’ Strong comprehension of clinical trial processes and study execution.

β€’ Exceptional organizational and project coordination abilities, capable of managing multiple tasks concurrently.

β€’ Strong written and verbal communication capabilities.

β€’ Experience in creating communications, newsletters, site-facing content, or engagement materials.

β€’ Proficiency in Microsoft Office, including the capacity to analyze and effectively present information.

β€’ Ability to thrive within global, cross-functional teams.

β€’ Employment is contingent upon possessing the legal right to work in the country where the position is located.

β€’ Preferred: experience in supporting global or multi-regional clinical trials.

β€’ Preferred: direct experience with study teams, investigators, sites, or clinical technology vendors.

β€’ Preferred: experience in delivering training, onboarding, or user support.

β€’ Preferred: knowledge of site engagement strategies and principles of change management.

β€’ Additional language skills would be a plus.


🏝️ Benefits

β€’ Competitive base salary along with performance-related incentives.

β€’ Health and wellness programs, including medical, dental, and vision coverage where applicable.

β€’ Retirement and pension plans.

β€’ Life assurance and disability coverage.

β€’ Employee assistance programs and wellness resources.

β€’ Opportunities for learning and development through structured training and career pathways.

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