Principal Clinical Data Scientist

Precision For Medicine

. Serve as the CSAI functional lead on assigned project teams .

Posted 10/6/2026full-timeRemote • United Kingdom, Hungary, Poland, Romania, Serbia, Slovakia, SpainLeadWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates extensive experience in clinical research management, including operational oversight of clinical science functions, data capture, and regulatory compliance. Proficient in managing cross-functional teams and budgets while ensuring adherence to quality standards in oncology research.

Highest-signal resume keywords

Clinical Research ManagementOncology ExpertiseElectronic Data Capture SystemsLeadership ExperienceFDA and ICH-GCP Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Data ReviewData Cleaning ProcessesProtocol ReviewFinancial Management SkillsECRF SpecificationsUAT DevelopmentMedical Terminology ProficiencyStudy Risk ManagementProject PlanningVariance Management

Soft Skills

Effective CommunicationTeam CollaborationProblem SolvingTraining and MentoringPresentation Skills

Tools & Technologies

Microsoft Office ProductsEDC SystemsETMF Documentation

Industry Keywords

Clinical Trial ProcessesSOPsRegulatory GuidanceStandards of CareGrading Criteria

About the role

Key responsibilities & impact

Serve as the CSAI functional lead on assigned project teams
Manage the operational clinical science function from study start-up through database lock
Provide scientific and clinical input into data capture, review, cleaning, eCRF specifications, edit checks, completion guidelines, and EDC UAT
Support and manage integrated cross-functional data-cleaning processes for interim and final study deliverables
Manage Medical Monitor review of subject data
Provide protocol review from a scientific operational perspective
Identify study risks and manage CSAI study-specific deficiencies
Support monthly invoicing and variance management of the CSAI budget
Manage CSAI resource needs and maintain project plans, guidelines, trackers, and eTMF documentation
Conduct holistic and aggregate clinical data review using programmed outputs, listings, metrics, and graphs
Oversee and resolve queries in EDC systems and report or escalate data review findings
Manage development and UAT of CSAI programmed outputs
Provide study-specific training and participate in internal and external meetings and presentations
Support data-related committees, TLF/CSR review, interviewing, business development, SOPs, trainings, and process improvement initiatives
Promote Precision’s quality and ethical image and perform other duties assigned by management

Requirements

What you’ll need

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
Experience with electronic data capture systems
Experience with Microsoft Office Products (Outlook, Word, Excel, PowerPoint)
Professional use of the English language, both written and oral
Ability to occasionally travel domestically and internationally including overnight stays
Highly advanced knowledge in oncology and medical terminology, including disease assessment criteria, standards of care, and grading criteria
Working knowledge of FDA and ICH-GCP, relevant SOPs, regulatory guidance, clinical trial processes, and clinical research functional departments
Ability to independently manage the CSAI operational function in a global, cross-functional environment
Ability to apply financial management skills at the functional area project level

Benefits

Comp & perks

Remote work arrangement
Opportunity to work in a global, cross-functional environment
Equal opportunity employment
Reasonable accommodation for applicants with disabilities