Unblinded Trial Delivery Specialist, Clinical Trial Coordinator - FSP

🔥 2 hours ago

🇵🇱 Poland – Remote

⏰ Full Time

🟢 Junior

🧪 Clinical Research

👻 Ghost score 12%

What it means: the chance that no one is really hiring for this job.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

🏥 Healthcare

Biotechnology • Pharmaceuticals • Healthcare

Thermo Fisher Scientific is the world leader in serving science, with a stated mission to enable customers to make the world healthier, cleaner and safer. The company provides a broad portfolio of laboratory instruments, analytical technologies, diagnostics, consumables, software and services that support life‑sciences research, analytical testing, clinical diagnostics and the development and manufacture of therapies. Its operations and offerings (as described on its site and in its news) include advanced imaging and electron microscopes, chromatography and mass‑spectrometry systems, genetic and clinical testing, lab automation and AI tools, bioprocessing and contract development/manufacturing services (brands cited include Thermo Scientific, Applied Biosystems, Invitrogen, Gibco, Fisher Scientific, Unity Lab Services, Patheon and PPD). Thermo Fisher reports annual revenue over $45 billion and emphasizes corporate social responsibility, environmental and community programs alongside its scientific products and services.

📋 Description

• Partner with Global Study Leaders to support end-to-end clinical trial delivery, ensuring alignment with study timelines, quality standards, budgets, and operational objectives. • Coordinate cross-functional study activities. • Oversee CROs and vendors. • Maintain study documentation and tracking systems. • Proactively identify, manage, and escalate risks to successful study delivery. • Coordinate unblinded study operations as the primary point of contact for uLDLs and uCRAs. • Support training, study documentation, and cross-functional communication. • Oversee unblinded risk management, including protocol deviations, accidental/emergency unblinding, safety escalations, and compliance with SOPs and study procedures. • Manage study oversight activities, including CTMS updates, IMP and ancillary supplies, third-party coordination, subject status reconciliation, and operational reporting. • Ensure TMF completeness, accuracy, and regulatory compliance through document reviews, quality checks, and CRO oversight. • Contribute to every stage of study delivery, from set-up to close-out.

🎯 Requirements

• Graduate/Bachelor's degree in life sciences or other related fields. • At least 1+ years of relevant work experience in a pharmaceutical environment. • Foundational knowledge of clinical study delivery processes, including regulations and industry standards. • Strong project management skills. • Excellent verbal and written communication in English. • Good knowledge of applicable clinical trial regulatory requirements. • Ability to manage multiple competing priorities and work independently. • Excellent collaborator coordination and communication abilities. • Proficient in Microsoft Office tools and clinical trial management systems.

🏖️ Benefits

• Opportunity to contribute to life-changing therapies. • Comprehensive training and development programs. • A collaborative and inclusive work environment. • Attractive compensation and comprehensive perks. • Tailored learning pathways. • Stretch assignments. • Mentorship. • Global exposure through international clinical studies across phases and therapeutic areas. • Opportunities to strengthen global project management, financial tracking, data analysis, and risk management abilities. • Opportunities to learn new clinical trial technologies such as AI platforms.

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume