Clinical Data Scientist Jobs

3 open positions found

View Health Data Scientist (AI & Clinical Data) (26-003)
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Health Data Scientist (AI & Clinical Data) (26-003)

Strategic Analysis, Inc. (SA) Is actively seeking a Health Data Scientist to provide technical leadership in data design, evaluation strategy, and clinical realism for a multi-stakeholder program advancing AI diagnostics for rare diseases. This is a Science and Engineering and Technical Advisor (SETA) role focused on ensuring that datasets, benchmarks, and evaluation methods are scientifically rigorous, clinically grounded, and aligned with real-world use. In this role, Health Data Scientist will operate at the intersection of health data, AI evaluation, and clinical practice, providing expert guidance to program leadership and external performers. You will help define what success means for AI diagnostics in rare disease contexts and ensure that technical progress translates into meaningful clinical insight and patient impact. This role is ideal for someone who combines deep experience with healthcare data and AI evaluation with the ability to critically assess methodologies, anticipate failure modes, and translate clinical realities into measurable technical criteria. Roles and Responsibilities: 1. Lead and advise on the design, preparation, and validation of healthcare datasets used across the program, including EHR, genomic, and multimodal data. 2. Define and assess evaluation strategies and benchmarks that are clinically realistic, methodologically sound, and resistant to shortcut learning or leakage. 3. Review technical proposals, model submissions, and evaluation results from external teams, providing expert feedback on validity, risks, and interpretability. 4. Assess data quality, representativeness, and bias, and advise on mitigation strategies appropriate to rare disease contexts. 5. Evaluate alignment between technical performance metrics and clinical decision-making needs, working closely with clinical SMEs. 6. Identify gaps between benchmark performance and real-world applicability, and advise on corrective actions. 7. Serve as a technical bridge between AI developers, clinical experts, and program leadership. 8. Support the program manager with technical assessments, recommendations, and decision support related to data and evaluation. 9. Track progress of external partners and identify data- or evaluation-related risks that could impact program outcomes. 10. Produce high-quality written reports, analyses, and presentations that communicate technical findings to diverse audiences. This role is suited to candidates who: * Think deeply about measurement, validity, and scientific rigor. * Are comfortable exercising judgment in ambiguous or under-specified evaluation contexts. * Maintain high standards for data quality and methodological integrity. * Communicate clearly across clinical, technical, and programmatic audiences. * Operate with ownership and accountability in high-stakes environments. * Are motivated by advancing AI systems that deliver real clinical and patient impact, not just strong metrics. Minimum Qualifications: * PhD in Biomedical Informatics, Data Science, Biostatistics, or a related field. * 5+ years of experience working with healthcare or biomedical data in applied or evaluative roles. * Hands-on experience with EHR, genomic, or multimodal healthcare datasets. * Deep understanding of AI/ML evaluation methods, including benchmarking, robustness, and sources of bias or leakage. * Demonstrated ability to critically review and assess technical work across health data and AI domains. * Strong understanding of data governance, privacy, and compliance in healthcare contexts. * Excellent written and verbal communication skills, with experience producing high-quality technical materials. Preferred Qualifications: * Domain expertise in rare disease, diagnostics, or clinical decision support. * Prior experience in technical advisory, evaluation, or SETA-style roles. * Experience collaborating closely with clinicians and healthcare stakeholders. * Experience working in fast-paced, multi-stakeholder, or early-stage environments. Education: PhD in Biomedical Informatics, Data Science, Biostatistics, or a related field. Location: Position is remote. Travel: Periodic travel may be required Clearance: Ability to obtain HHS Public Trust.

8 months agovia universal intelligenceApply ›
View Clinical Data Scientist
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Clinical Data Scientist

Overview: ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. We are currently seeking a Senior Statistical Programmer I/Data Scientist to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial data and supporting the statistical analysis process to ensure high-quality results. You will contribute to the success of our clinical studies by developing and validating statistical programs, collaborating with biostatisticians, and ensuring compliance with regulatory standards. Responsibilities: Developing and validating R-Shiny programs for statistical analysis and reporting of clinical trial data. Collaborating with biostatisticians to define analysis plans and statistical methods to be applied to clinical data. Performing quality control checks on statistical outputs and ensuring accuracy and consistency in reporting. Contributing to process improvements by identifying efficiencies in programming practices and methodologies. Qualifications: Bachelor’s or Master’s degree in Statistics, Mathematics, Computer Science, or a related field. 5 + years of Experience in statistical programming, preferably in a clinical research or pharmaceutical setting. Strong proficiency in SAS, R, R-Shiny or Python programming, with a solid understanding of statistical concepts and methodologies. Excellent analytical and problem-solving skills, with a keen attention to detail. * Strong communication skills, with the ability to work collaboratively in a team environment and effectively convey complex information.

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View Principal Clinical Data Reviewer/Scientist
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Principal Clinical Data Reviewer/Scientist

BiogenResearch Triangle Park, NC, US

About This Role As a Principal Clinical Data Reviewer/Scientist, you will play a critical leadership role in ensuring the integrity, scientific rigor, and strategic value of clinical trial data across all phases of development. You will apply deep clinical and scientific expertise to assess data quality, plausibility, and completeness, while proactively identifying trends, signals, and potential risks related to study endpoints and patient safety. What You’ll Do Lead clinical and scientific data review activities across assigned clinical studies, ensuring data accuracy, consistency, and alignment with protocol expectations and therapeutic objectives. Identify insights, trends, and risks through comprehensive data analysis and interpretation, enabling early detection of data quality issues and safety signals. Design, test, and refine clinical data review tools—including listings, reports, and visualizations—to support robust data exploration, signal detection, and discrepancy management. Collaborate closely with cross‑functional teams, including Clinical Development, Biostatistics, Pharmacovigilance, and Study Operations, to drive data‑driven decision‑making and ensure high-quality trial execution. Manage timelines and deliverables with a strong commitment to quality, efficiency, and proactive communication. Contribute to risk management by identifying, documenting, and supporting mitigation of study‑level data risks. Support strategic initiatives within and beyond the Data Management organization, bringing scientific and operational insight to process innovation and continuous improvement. Leverage metrics and analytics to monitor data trends, assess study health, and enhance data review strategies. Who You Are You have a strong passion for scientific data excellence and clinical research quality. You possess strong analytical skills with the ability to translate complex data into actionable insights. You have a strong collaborative mindset with the ability to work effectively across multifunctional teams. You are committed to maintaining the highest quality execution and continuous improvement in data review practices. Required Skills 5+ years in a Clinical Operations/Clinical Scientific role, or in DM in industry or Academia with strong scientific knowledge in at least one therapeutic area within Biogen portfolio. Robust experience with Medidata Rave and use of Data Review tools such as eClinical Elluminate, J-Review, or Business Objects required High attention to detail including proven ability to manage multiple, competing priorities Experience supporting audits/inspections Excellent written and oral communication skills Ability to work under pressure demonstrating agility through effective and innovative team leadership Deep understanding of drug development and biopharmaceutical industry required Strong technical skills, including experience working with using Microsoft Excel functionality Fluent English (oral and written) Hands‑on experience reviewing eCRF data, external data sources (e.g., labs, imaging, biomarkers, digital health), and integrated clinical datasets. Demonstrated ability to identify data trends, signals, outliers, and risk indicators using listings, visualizations, metrics, and analytics tools. Experience with CDISC standards (SDTM, ADaM) and familiarity with clinical analytic tools (visualization platforms). Strong knowledge of GCP, ICH E6(R2)/E6(R3), regulatory expectations, and industry data quality best practices. Demonstrated problem‑solving skills with a continuous improvement mindset and enthusiasm for scientific data excellence. Education Requirements/Preferred Skills Bachelor’s degree in life sciences, health sciences, pharmacy, nursing, data science, or related discipline; advanced degree (MS, PharmD, PhD) strongly preferred. Experience with implementing consistent clinical and scientific data review processes. Ability to highlight and mitigate performance and quality issues with vendors. Previous experience in coordinating timelines and data deliverables across multiple studies/programs. Why Biogen? Our mission to find therapies for neurological and rare diseases is a unique focus within our industry and this shared purpose is what connects us as a team. We work together to overcome obstacles and to follow the science. We are resilient as we strive to make an impact on our patients’ lives and on changing the course of medicine. Together, we pioneer. Together, we thrive. Job Level: Management Additional Information The base compensation range for this role is: $116,000.00-$155,000.00 Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills \& experience, job location, and internal equity. Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being ; including, but not limited to: Medical, Dental, Vision, \& Life insurances Fitness \& Wellness programs including a fitness reimbursement Short- and Long-Term Disability insurance A minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31) Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar year Paid Maternity and Parental Leave benefit 401(k) program participation with company matched contributions Employee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year * Employee Resource Groups participation Why Biogen? We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives. At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE\&I efforts. All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

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Clinical Data Scientist Jobs | Jobfu