Principal/Senior Clinical Data Scientist

🕒 October 6

🌐 United Kingdom, Hungary, +5 more countries – Remote

🇬🇧 United Kingdom – Remote 🇭🇺 Hungary – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇷🇸 Serbia – Remote 🇸🇰 Slovakia – Remote 🇪🇸 Spain – Remote

⏰ Full Time

🟠 Senior

📊 Data Scientist

👻 Ghost score 30%

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

Precision For Medicine

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

💰 $75M Private Equity Round on 2015-12

Healthcare • Consulting • Logistics

Precision For Medicine is a leading organization that specializes in supporting the development and commercialization of innovative therapies, particularly in oncology, rare diseases, and autoimmune conditions. With a comprehensive range of services including clinical trial management, lab services, and biospecimen collection, they integrate advanced biomarker capabilities and manufacturing solutions to streamline the complex clinical development processes. Their mission is to accelerate research and bring life-changing medical solutions to patients by overcoming traditional inefficiencies typically found in the pharmaceutical development landscape.

📋 Description

• Lead the clinical science function across assigned Oncology, Rare Diseases, and/or Autoimmune clinical development programs from study start-up through database lock • Provide scientific and indication-specific expertise for clinical trial data collection, review, interpretation, and issue resolution • Perform holistic individual and aggregate participant data review using proprietary and non-proprietary tools and platforms • Support data capture, query management, clinically relevant data cleaning, and participant safety • Serve as clinical and scientific subject matter expert for eCRF design, data capture requirements, edit checks, completion guidelines, EDC UAT, and ongoing data review • Support Risk Based Quality Management by identifying and addressing study risks, trends, and issues • Collaborate with Medical Monitoring and oversee Medical Monitor review of participant data and findings • Provide scientific-operational protocol review • Support project and financial management, invoicing, and out-of-scope management • Collaborate with Clinical Science management regarding resource needs • Develop and maintain project plans, guidelines, trackers, and programming specifications for data review tools and outputs • Maintain applicable eTMF documentation accurately • Participate in internal and external study meetings and presentations, including facilitating Medical Data Review Meetings • Contribute to study-level strategy, data review processes, and continuous improvement initiatives • Support business development activities, including bid defense meetings and presentations • May review tables, figures, listings, and clinical study reports

🎯 Requirements

• Bachelor’s degree or equivalent combination of education/experience in science or health-related discipline with proficiency in medical terminology • Minimum of 8 years of clinical research experience or proven competencies for this position • Minimum of 3 years Oncology experience, within the past 1.5 years • Minimum of 1 year of leadership experience • High proficiency with Microsoft Office Products (Outlook, Word, Excel, PowerPoint, Teams, OneNote) • Professional use of the English language, written and oral • Ability to occasionally travel domestically and internationally, including overnight stays, up to approximately 25% • Highly advanced knowledge in oncology and medical terminology • Working knowledge of FDA, ICH-GCP, relevant SOPs, regulatory guidance, and the clinical trial process • Ability to independently manage Clinical Science operations in a global, cross-functional environment • Preferred: medical-related degree, RN, OCN, RPH, PharmD, EDC systems, database build, monitoring/data review, data visualization platforms, phase I–III and global studies

🏖️ Benefits

• Ability to work remotely • Opportunity to work on global clinical development programs • Occasional domestic and international travel • Equal opportunity employer • Reasonable accommodation support for applicants with disabilities

📊 Check your resume score for this job

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

Upload Resume