Senior Research Associate – Clinical Outcomes Assessment, In-Trial Research

🕒 October 16

🌐 United Kingdom, France, +4 more countries – Remote

🇬🇧 United Kingdom – Remote 🇫🇷 France – Remote 🇮🇹 Italy – Remote 🇵🇱 Poland – Remote 🇪🇸 Spain – Remote 🇭🇺 Hungary – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.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

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

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

Upload Resume

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

• Provide scientific leadership within project teams independently and/or collaboratively with research scientists • Serve as lead author, co-author, or internal reviewer of client deliverables, including study protocols, final reports, literature reviews, statistical analysis plans, PRO evidence dossiers, poster presentations, and manuscripts • Interact substantially with clients through face-to-face meetings and teleconferences • Provide timely status updates and escalate issues • Formulate project work plans and ensure timelines are met within scope and budget • Train and mentor junior-level staff • Draft abstracts, posters, oral presentations, and manuscripts • Design qualitative-data analysis plans and generate client-ready reports • Identify staff resources, present scopes of work, and direct teams with feedback • Manage internal timelines and project budgets/staff hours • Lead, review, and finalize project proposals, including budgets • Attend and present at scientific conferences • Develop and present internal scientific trainings • Participate in staff recruitment efforts • Assist PIs in preparing clients for regulatory meetings

🎯 Requirements

• Doctorate Degree (e.g. PhD; D.Ph.; Pharm D) in science discipline; or Master’s degree in science discipline, with at least 5 years’ experience in a relevant field; or Bachelor’s degree with at least 7 years’ experience in a relevant field • Ability to manage or direct large portfolio of projects in terms of dollar volume and number of projects • Understanding of relevant qualitative and quantitative methodology • Ability to work well within diverse project teams • Excellent communication and scientific writing skills, demonstrated by peer-reviewed publications, technical reports, or other scholarly work • Strong analytical and problem-solving skills

🏖️ Benefits

• Global team environment • Collaboration and development opportunities • Scientific excellence-focused work environment