Principal/Senior Clinical Data Scientist

🕒 May 11

🌐 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 76%

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Precision Medicine Group

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 2012

💼 Consulting

🏥 Healthcare

📦 Logistics

💰 $35.2M Venture Round on 2021-03

Consulting • Healthcare • Logistics

Precision Medicine Group is a global team of experts that specializes in precision medicine, which combines advanced lab sciences, translational informatics, regulatory affairs, payer insights, and marketing communications. The company focuses on overcoming product development and commercialization challenges for pharmaceutical and life sciences clients. Their services include biomarker-driven research and development, as well as commercialization support for life science organizations from launch to product maturity. Precision Medicine Group operates through two main arms: Precision for Medicine and Precision AQ, specializing in clinical and commercial solutions respectively.

📋 Description

• Lead the clinical science function across assigned Oncology, Rare Diseases, and/or Autoimmune clinical development programs from study start-up through database lock • Serve as a functional team lead and deliver Clinical Science services within scope, timelines, and budgets • Perform holistic individual participant and aggregate participant data review using proprietary and non-proprietary tools and platforms • Identify, evaluate, and resolve clinical data issues; support data capture, query management, interpretation, and data cleaning • Serve as the scientific and clinical data subject matter expert for study teams • Guide eCRF design, data capture requirements, edit checks, completion guidelines, EDC UAT, and ongoing clinical data review • Support Risk Based Quality Management by identifying and addressing study risks, trends, and issues • Collaborate with Medical Monitoring and oversee 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 on resource needs • Develop and maintain Clinical Science plans, guidelines, trackers, and programming specifications • Maintain applicable eTMF documentation • Participate in internal and external study meetings and presentations, including Medical Data Review Meetings • Contribute to study-level strategy, data review processes, and continuous improvement initiatives • Support business development activities and may review TLFs 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 of 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 and ICH-GCP, relevant SOPs, regulatory guidance, and the clinical trial process • Ability to independently manage Clinical Science operations in a global, cross-functional environment • Ability to apply financial management skills at the functional area project level • Preferred: medical-related degree, RN, OCN, RPH, PharmD, EDC systems experience, database build experience, on-site/monitoring/data review experience, data visualization tools, phase I–III and global studies experience

🏖️ Benefits

• Ability to work remotely • Opportunity to occasionally travel domestically and internationally, including overnight stays (up to approximately 25%) • Equal opportunity employment

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