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Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # Principal Clinical Data Scientist - **Company:** Precision for Medicine - **Location:** UK (Remote available) - **Contract:** Contract - **Skills:** Microsoft Word, Microsoft Excel, Microsoft Outlook, Clinical Data Management, Clinical Data Repository, Computer Programming, Databases, Data Cleansing, Data Visualization, Electronic Data Capture, Microsoft Office, Microsoft PowerPoint, Data Management - **Published:** October 6, 2026 - **Apply:** https://www.indeed.com/viewjob?jk=0544634867f26b01 ## About the Role * 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 1 year of leadership experience Other Required: * Experience with electronic data capture systems * Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint) * Excellent communication & interpersonal skills to effectively interface with others in a team setting * Excellent organization skills, attention to detail & a customer service demeanor * Professional use of the English language; both written & oral * Ability to occasionally travel domestically & internationally including overnight stays Preferred: * Medical related degree, RN, OCN, RPH, PharmD, etc. * Database build experience * On-site monitoring experience &/or data review experience * Experience with data visualization software such as JReview * Experience in solid & liquid tumors * Experience in phase I, II & III studies * Experience in global trials Skills & Competencies: * Demonstrates highly advanced knowledge in oncology & medical terminology with ability to apply knowledge to clinical trial data including the application of disease assessment criteria, standards of care, grading criteria, etc. * Desire to continually learn & keep up to date on medical & oncology standards of care with the ability to self-research & educate. * Working knowledge of FDA & ICH-GCP, relevant SOPs & regulatory guidance with a well-rounded knowledge of the entire clinical trial process & working understanding of clinical research functional departments * High level of integrity from a professional & ethical perspective * Ability to independently manage the CSAI operational function in a global, cross-functional environment with awareness of appropriate escalation. * Excellent time management, negotiation, critical thinking, decision making, analytical &conflict management skills with the ability to strategically plan & apply effective risk management. * Exhibits self-motivation with the ability to work remotely while independently lead, support & inspire excellence. * Demonstrates ability to adjust to multiple demands & shifting priorities. * Results oriented, accountable, motivated, cooperative, & flexible * Ability to apply financial management skills at the functional area project level. * Excellent presentation, verbal, & written communications skills, Candidates must be legally authorized to work in the country of employment without employer sponsorship. ## Description The Principal Clinical Scientist, Clinical Science Analytics & Insights is responsible for & manages the operational clinical science function from study start up through database lock for assigned projects focused on the scientific & indication specific insights into data collection & data visualization outputs to support scientific, clinical-sense data cleaning as part of Precision's cross-functional data review team. Serves as the subject matter expert in the application of clinical knowledge, guidelines & standards of care to the review of clinical trial data. Serves & contributes to project teams as the CSAI functional lead delivering within scope, time & cost., * Serve as the functional lead implementing CSAI services per study scope of work (SOW) on assigned project team(s) * Serve as a resource for project teams regarding scientific related data capture, review & cleaning. * Support & participate in the development & implementation of process flow for integrated, cross[1]functional, data cleaning for interim &/or final study data deliverables between all applicable departments (e.g., data management, medical, safety, vendors, sponsor, etc.) * May be responsible to cross-functionally manage the overall data cleaning process internally to support interim &/or final data deliverables (e.g., tier cleaning process/timelines, etc.) * Manage Medical Monitor review of subject data. * Provide protocol review from a scientific operational perspective. * Provide indication-focused, scientific, clinical input & support to Data Management in the development & revision of eCRF specifications, edit checks & completion guidelines &/or other study[1]specific documentation as applicable. * Provide indication-focused, scientific, clinical input & support to Data Management in the conduct of EDC UAT supporting the CSAI function as applicable. * Collaborate to support cross-functional departmental communication including internal CSAI communication as applicable on data capture, review trends, EDC updates, CSAI Programming needs, etc. * Support the identification of study risks including the management to correct any CSAI study-specific deficiencies. * Support Project & Financial Management on monthly invoicing & variance management of the CSAI budget * Collaborate with CSAI management to ensure that CSAI resource needs are adequately addressed due to scope of work changes. * Oversee &/or develop & maintain CSAI project related plans, guidelines, & trackers * Ensure applicable eTMF documentation related to CSAI is maintained as per study project plans & SOPs. * Support &/or conduct holistic &/or aggregate scientific, clinical sense data review based on defined manual Clinical Data Review Guidelines using various programmed outputs including but not limited to Smart Patient Profiles , Smart All-Patient-Data Workbook, listings, quality metrics &/or graphs. * Oversee &/or issue & resole queries in various EDC systems. * Review &/or provide routine status updates on CSAI data review findings & escalate issues as appropriate. * Manage &/or conduct the development & associated User Acceptance Testing (UAT) of CSAI programmed output(s) * Provide study-specific training for CSAI Scientists, project teams &/or study sites based on review findings. * Participate in internal & external study-specific team meetings &/or presentations as applicable including facilitating CSAI meetings or topics. * May support study-specific data related committees &/or meetings (e.g., safety review committee) * May conduct review of Table, Figure & Listings (TLFs) &/or clinical study reports (CSRs) * May participate in the interview process of potential new CSAI candidates. * May participate in business development activities including proposal development & client presentations as applicable. * Serve as an ambassador to promote Precision's high quality & ethical image in accordance with the company Core Values * May develop &/or review of SOPs. * May develop &/or present departmental trainings. * Contribute to & support company & CSAI process improvement initiatives. * Performs other duties as assigned by management.