Senior Clinical Data Manager

🔥 14 hours ago

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

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

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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

• Manage all aspects of the clinical trial data management process from study startup through post-database lock for assigned projects • Follow SOPs/WIs, regulatory directives, study-specific plans, and guidelines • Serve as primary Data Management contact or Lead DM for assigned clinical projects/programs • Oversee project data entry, including guidelines, training, quality, and resourcing • Assess and manage timelines, deadlines, and resource needs • Develop CRF specifications and coordinate stakeholder review when required • Conduct database build UAT and maintain controlled database documentation • Oversee clinical database quality and edit-check specifications • Create, revise, version, and maintain data management documentation and Trial Master File documentation • Train clinical research personnel and data management project team members • Review and query clinical trial data according to the Data Management Plan • Perform line-listing data review and patient/study-level status and metric reporting • Perform medical coding and coordinate SAE/AE reconciliation • Liaise with external data and EDC vendors regarding timelines and data-related deliverables • Assist with SAS programming and quality control of SAS programs when needed • Identify and troubleshoot operational problems using metrics, audit reports, and stakeholder input • Review and provide feedback on protocols, SAPs, and CSRs when required • Participate in SOP and process documentation development and maintenance • Support strategy meetings, bid defenses, capability presentations, client engagement meetings, RFP reviews, proposals, and project estimates • Provide leadership for cross-functional and organization-wide initiatives • Communicate with sponsors, vendors, and project teams regarding project issues • Present software demonstrations, trainings, and project meetings • Perform other assigned duties

🎯 Requirements

• Bachelor's degree and/or a combination of related experience • 8+ years’ experience as a Senior Clinical Data Manager or 5+ years as a Clinical Data Manager II working for a Clinical Research Organisation, Pharmaceutical or Biotech company • Experience with setup and database migrations • Oncology experience preferred • Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook • Professional use of the English language, written and oral • Experience using various clinical database management systems • Broad knowledge of drug, device and/or biologic development and effective data management practices • Strong representational, organizational, communication, leadership, and interpersonal skills • Ability to undertake occasional travel • Must be legally authorized to work in the country of employment without employer sponsorship

🏖️ Benefits

• Equal Opportunity Employer • Reasonable accommodation available for applicants with disabilities • Some travel may be required • AI-generated insights during the application journey with an opt-out option