Remote Life Science Jobs at ICON, Czech Republic | Apply Online
If you are an early-career life scientist, a regulatory affairs enthusiast, or a recent graduate looking to enter clinical trial operations, this full-time role at ICON plc is an exceptional opportunity. Offered as a remote, home-based position in Prague, Czech Republic, this role places you on the front lines of site activation and regulatory compliance. For organized professionals searching for a high-impact entry-level Life Science Jobs track, this position provides hands-on mastery over Clinical Trial Applications (CTAs), ethics committee submissions, and stakeholder coordination. It serves as an elite launchpad to develop a long-term ICON Career and stands out as a premier choice for anyone looking to secure a high-growth Job in Prague within a leading global Contract Research Organization (CRO).
About The Company
ICON plc is a world-leading healthcare intelligence and global Contract Research Organization (CRO) driven by a unified mission to accelerate the development of innovative medicines, medical devices, and diagnostic tools. Managing multi-center operations across North America, EMEA, and APAC, ICON provides the underlying regulatory, clinical, and data infrastructure that helps pharmaceutical innovators combat global diseases. This specific vacancy is hosted within ICON Strategic Solutions, operating under a highly collaborative Functional Service Provider (FSP) model. In this setup, you are embedded directly into a single, major global pharmaceutical sponsor’s internal study delivery infrastructure. This architecture allows you to focus exclusively on that sponsor’s specific pipeline protocols, proprietary clinical technologies, and site activation workflows, while simultaneously enjoying the job security, international network, and comprehensive employee benefits provided by ICON.
Remote Life Science Jobs – Key Responsibilities
The Study Start-Up Associate I functions as a vital operational engine, facilitating the rapid initiation of clinical trials and ensuring strict compliance with local and international regulatory requirements.
Your core regulatory tracking, document auditing, and cross-functional coordination duties include:
- Dossier Preparation & Submission: Assisting in the compilation, review, and submission of critical regulatory documents, including clinical trial applications (CTAs) and ethics committee dossiers.
- Stakeholder Coordination: Liaising with internal project managers and external clinical site staff to obtain necessary approvals, financial sign-offs, and authorizations required for study initiation.
- Regulatory Compliance Tracking: Maintaining accurate, real-time records of regulatory submissions, queries, and health authority approvals to advance this Life Science Jobs pathway.
- Core Document Development Support: Supporting clinical study teams in the secondary preparation of trial-related documents, including protocols, informed consent forms (ICFs), and investigator brochures (IBs).
- Start-Up Timeline Management: Participating actively in study start-up meetings, tracking site activation milestones, and providing input on local regulatory timelines to support your ICON Career.
Qualifications & Profile Requirements For Remote Life Science Jobs
ICON seeks a highly structured, analytical individual who demonstrates an exceptional eye for detail and can manage multiple tasks simultaneously in a fast-paced environment.
- Required Academic & Experience Criteria:
- Educational Foundation: A completed formal University degree (Bachelor’s degree) in the Life Sciences or a closely related natural scientific/healthcare discipline.
- Experience Tier: Previous experience in clinical research or regulatory affairs is preferred, but not required. This role is fully open to early talent with strong transferable organizational skills.
- Linguistic Mastery: Full professional fluency in written and verbal English, paired with professional proficiency in Czech to manage local regulatory bodies and hospital staff for this Job in Prague.
- Core Technical & Interpersonal Skills:
- Strong attention to detail, proactive problem-solving habits, and a highly organized approach to file management.
- Excellent communication and interpersonal skills, with the demonstrated ability to collaborate effectively across highly matrixed, cross-functional teams.
- Good command of digital workspace tools (including Microsoft Excel, Word, and document management systems).
- Mobility Parameters: Willingness and capability to accommodate occasional domestic travel as required by study start-up timelines (approximately 5%).
In short, the Study Start-Up Associate I position within ICON’s FSP framework is a definitive route to transitioning your life sciences degree into a premium global clinical operations asset. Securing an appointment here allows you to bypass general laboratory work and take direct operational charge of the clinical trial applications, ethics dossiers, and site activation timelines that bring next-generation therapies safely to life. If you reside in the Czech Republic, hold a life sciences degree, and possess an compromise-free commitment to protocol tracking, apply today to secure this premier Life Science Jobs vacancy, launch an exceptional ICON Career, and lock in this outstanding Job in Prague.
