Country Approval Specialist II

🕒 September 23

🌐 Denmark, Norway, +1 more countries – Remote

🇩🇰 Denmark – Remote 🇳🇴 Norway – Remote 🇸🇪 Sweden – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🏥 Clinical Operations

👻 Ghost score 14%

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.

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Thermo Fisher Scientific

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1956

🏥 Healthcare

📦 Logistics

🏭 Manufacturing

Healthcare • Logistics • Manufacturing

Thermo Fisher Scientific is the world leader in serving science, with annual revenue of more than $40 billion. Their mission is to enable customers to make the world healthier, cleaner, and safer by supporting life sciences research, solving complex analytical challenges, increasing laboratory productivity, and improving patient health through diagnostics and the development of life-changing therapies. With a global team, they offer innovative technologies and pharmaceutical services through brands such as Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD.

📋 Description

• Prepare, review, and coordinate local regulatory submissions in alignment with the global submission strategy • Provide local regulatory strategy advice to internal clients under guidance • Provide and coordinate project-specific local SIA services • Contact investigators for submission-related activities as needed • Act as country-level key contact for ethical or regulatory submission-related activities • Coordinate with internal functional departments on site start-up activities and submission timelines • Ensure submission processes align with critical paths for site activation • Achieve target cycle times for site activities • Work with start-up CRAs to prepare regulatory compliance review packages as applicable • Develop country-specific Patient Information Sheets and Informed Consent Forms as needed • Assist with grant budget and payment schedule negotiations with sites • Support feasibility activity coordination according to agreed timelines • Enter and maintain trial status information for SIA activities in tracking databases • Prepare, set up, and maintain local country study files and filing processes • Maintain knowledge of company and client SOPs, directives, and applicable regulatory guidelines

🎯 Requirements

• Bachelor's degree or equivalent and relevant formal academic / vocational qualification • 2+ years of previous experience providing the knowledge, skills, and abilities to perform the job • Effective oral and written communication skills • Excellent interpersonal skills • Strong attention to detail and quality of documentation • Good negotiation skills • Good computer skills and ability to learn appropriate software • Good English language and grammar skills • Basic medical/therapeutic area and medical terminology knowledge • Ability to work in a team environment or independently, under direction, as required • Basic organizational and planning skills • Basic knowledge of applicable regional/national country regulatory guidelines and EC regulations • Ability to work Monday-Friday standard schedule • Willingness and ability to work in office/laboratory and/or clinical environments, with potential exposure to biological fluids, infectious organisms, and electrical office equipment • Ability to use required personal protective equipment, including protective eyewear, garments, and gloves

🏖️ Benefits

• Full-time employment • Fully remote work arrangement

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