Clinical Data Analyst Job at Solomon Page (Clark)

Clinical Data Analyst

We are hiring a Clinical Data Scientist to lead the generation of credible, clin...

Location

United States

Salary:

110000.00 - 140000.00 USD / Year

Calibrate

Expiration Date

Until further notice

Requirements

5+ years of experience analyzing clinical or healthcare outcomes data
Experience analyzing data over time and working with cohort based analyses
Proficiency in SQL and Python or R
Hands on experience with DBT and data modeling
Proficiency with using a data reporting software (e.g. Tableau, Microsoft Power BI, Looker,etc.)

Job Responsibility

Design and analyze clinical outcome studies evaluating weight loss and durability, medication adherence, metabolic and cardiometabolic risk indicators, and safety or clinical escalation patterns
Build analyses that define the right cohorts, starting points, and follow up timelines to measure program impact
Partner closely with Clinical leadership to evaluate treatment pathways, protocol adherence, and the timing and intensity of clinical touchpoints
Assess the impact of clinical interventions on outcomes and overall member experience
Use insights to inform and continuously improve clinical protocols and program design
Contribute to building internal evidence frameworks that define and measure clinical effectiveness within our care model
Translate analytic findings into clear, practical insights that support clinical and operational decision making
Ensure analyses align with accepted clinical standards and are appropriate for clinical leadership, employer, and partner audiences
Produce documentation and outputs that can withstand external scrutiny and support potential presentations or publications
Partner with Data Engineering to define clinical data requirements, quality standards, and analytic definitions

What we offer

Generous paid time off policy, including multiple paid company holidays, wellness days, and floating holidays
Medical, dental, and vision benefit options
Calibrate-funded disability and basic life insurance
Access to several wellness programs, including a complimentary Headspace membership, and therapy on your schedule with Headspace Care
Employee Assistance Program through Prudential
Remote-first ways of working, with the flexibility to work from any state
Competitive paid parental leave program

Fulltime

Clinical Data Analyst

AB Science is hiring a Clinical Data Analyst based in Paris. Responsibilities co...

Location

France , Paris

Salary:

Not provided

AB SCIENCE

Expiration Date

Until further notice

Requirements

Male or female with University degree (MSc or PhD) in Pharmacy, Pharmacology, Life Sciences or related discipline
At least 5 years of experience in Clinical trials, preferably in Clinical Data Management
Knowledge of clinical development process
Understanding of regulatory guidelines in a pharmaceutical research setting, including ICH GCP training
Sound familiarity with Office automation tool (i.e. Excel, Word, Power point)
Knowledge of database programming tool is a plus (i.e. SQL, MS Access, SAS, etc.)
MedDRA coding certification is a plus
WHODD coding certification is a plus

Job Responsibility

Ensure the clinical consistency of data used for statistical analyses and clinical study reports
Clinical data to be check includes laboratory results, adverse events, medical history, vital signs, efficacy measurements and treatments
Follow-up the resolution of detected issues/inconsistencies via queries process
Participate to the development and maintenance of core study documents pertaining to the section, e.g. the CRF, CRF Completion Guidelines, Data Validation Specifications, Data Management Plan, Data Review Plan
Ensure Clinical Data Management input to other relevant strategic study documents and vendor contracts
Detect important medical events
Perform reconciliation of SAE and AE of Special Interest between the Pharmacovigilance database and the Clinical Study Database
Detect the forbidden concomitant treatments as per study protocol
Develop and track timelines to ensure data management milestones are met in coordination with the Clinical and Pharmacovigilance Team
Archive documents in the clinical data management TMF

What we offer

Permanent position
Salary & package to define according skills and experience

Fulltime

Clinical Data Analyst

This is a long-term contract position within the healthcare industry, offering a...

Location

United States , Minnetonka

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Minimum of 5 years of experience in clinical informatics
At least 2 years of experience in business analysis
2 years of hands-on experience in data analysis
Expertise in Agile methodologies and software development life cycle (SDLC)
Familiarity with clinical chart interpretation and gap analysis
Proficiency in tools such as SQL and Aha
Strong knowledge of healthcare systems, including Medicare and TRICARE
Ability to collaborate effectively with cross-functional teams and stakeholders

Job Responsibility

Define and document requirements for technology consumption
Translate business requirements into actionable features using tools like Aha
Prioritize features and collaborate with technology teams
Provide input and feedback to refine technology outputs
Review and analyze clinical charts to identify evidence of data and interpret information for closing care gaps
Test and validate development outputs
Collaborate with cross-functional teams to improve healthcare quality measures and reporting
Utilize business analysis and data analysis techniques to support clinical and operational objectives
Contribute to the development and enhancement of software solutions within an Agile framework
Interpret healthcare data and provide actionable insights to support decision-making and process improvement

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

Lead Data Scientist - Clinical Informatics (Clinical Data Standards)

We’re building a world of health around every individual — shaping a more connec...

Location

United States , New York

Salary:

130295.00 - 260590.00 USD / Year

CVS Health

Expiration Date

June 29, 2026

Requirements

7+ years of relevant experience in clinical informatics, healthcare analytics, or clinical data management
Deep expertise in clinical data types and structures, including CCD data, lab results, clinical notes, and administrative healthcare data
Strong knowledge of clinical coding systems and terminologies, such as ICD-10, CPT, HCPCS, SNOMED-CT, LOINC, NDC, and RxNorm
Experience designing and documenting data models, taxonomies, or classification frameworks for clinical or healthcare data
Proven ability to enable and support downstream data consumers (analysts, data scientists, business users) through documentation, training, and consultative support
Experience leading cross-functional projects from concept to delivery by coordinating across clinical, technical, and business stakeholders
Proficiency with SQL and experience working with large-scale healthcare datasets
Experience using cloud-based data platforms, preferably Google Cloud Platform (GCP) tools including BigQuery, for querying, transforming, and managing data
Strong understanding of data quality principles, including validation, profiling, and monitoring of healthcare data
Excellent written and verbal communication skills, including the ability to explain complex clinical data concepts to both technical and non-technical audiences

Job Responsibility

Serve as a subject matter expert in clinical data, including CCD data, with deep understanding of how to structure and apply this data to solve healthcare problems
Design and maintain clinical data models, taxonomies, and classification frameworks that enable consistent interpretation and use of clinical data across the organization
Develop and govern the clinical data feature store, establishing standards, documentation, and best practices that accelerate adoption of clinical data for downstream analytics, reporting, and AI/ML use cases
Enable self-service analytics by building well-documented, validated, and reusable data assets (tables, views, features) that empower analysts and data scientists to work independently with clinical data
Create and maintain comprehensive data documentation, including data dictionaries, lineage, business logic, known limitations, and appropriate use guidelines for clinical datasets
Build queries, dashboards, and data visualizations to effectively communicate data quality metrics, data availability, and clinical insights to technical and non-technical stakeholders
Partner with clinical, operational, and business stakeholders to understand their data needs, translate requirements into data solutions, and ensure clinical data assets meet their analytical objectives
Lead and mentor data scientists, data analysts, and data engineers, providing guidance on clinical data interpretation, appropriate use, and best practices for working with healthcare data
Establish data quality frameworks for clinical data, including validation rules, anomaly detection, and monitoring processes to ensure data integrity and reliability
Translate clinical concepts into analytical frameworks, ensuring that business partners understand the capabilities and limitations of available clinical data

What we offer

Medical, dental, and vision coverage
Paid time off
Retirement savings options
Wellness programs
CVS Health bonus, commission or short-term incentive program
Award target in the company’s equity award program

Fulltime

Senior Clinical Data Analyst

Parexel is currently seeking a Senior Clinical Data Analyst to join us in either...

Location

United Kingdom; Poland; South Africa , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Bachelor's Degree required, preferably in the scientific/healthcare field
Proven leadership experience
Good project management skills and a proven ability to multitask
At least five years' or preferably up to 8 years' experience, in Data Management for the pharmaceutical/biotechnology industry
Understanding of the scope and focus of Phase I – IV clinical studies, and a proven ability to perform some of the core Data Management tasks and interact with vendors
A high level of Phase I experience is essential
A comprehensive understanding of regulatory guidelines and industry standards (e.g., ICH/FDA guidance, CDISC standards, GCDMP, 21 CFR 11, MedDRA, WHO Drug Dictionaries, etc.) and their application to Data Management practice
Attention to detail and the ability to work individually, within a multi-disciplinary team, as well as with external partners and vendors
Strong English language written and verbal communication skills
Able to travel to meetings or training seminars on occasion

Job Responsibility

Lead a large clinical study or a series of related studies with minimum guidance
Represents Data Management on the CTWG for assigned studies
Provide mentoring and training to lower-level Data Management staff assigned to your studies
Manage and monitor the progress of data management activities with CROs or other vendors on assigned studies
build effective relationships with CRO / vendor counterparts
Review protocols for appropriate data capture including electronic Case Report Form (eCRF) design
Be able to perform a thoroughly detailed review of eCRF data requirements
Interact with CRAs, programmers, study managers and statisticians in designing eCRFs and creating the annotated eCRF and CRF completion guidelines
Lead the development of data edit check specifications and data listings
Coordinate the design and testing of Electronic Data Capture (EDC) systems according to company standards

What we offer

annual performance-based bonus plan
annual salary review
total rewards incentives

Fulltime

Pyxis Data Analyst - Clinical Pharmacy

Serves as a liaison and resource for all departments that utilize Pyxis and the ...

Location

United States , Tucson

Salary:

Not provided

Tucson Medical Center

Expiration Date

Until further notice

Requirements

Bachelor's degree in business or a related field or an equivalent combination of relevant education and experience
five years of contracts or materials management experience
FOR PHARMACY: Associate degree or equivalent from two-year College or technical school, requires three years pharmacy technician experience
FOR PHARMACY: Must be licensed and registered by the Arizona State Board of Pharmacy as a Pharmacy Technician
Knowledge business system requirements and documentation practices
Skill in evaluating business systems, documenting solutions and trouble shooting problems
Skill in training and guiding others
Ability to read, analyze and interpret general business periodicals, professional journals, technical procedures, or governmental regulations
Ability to prepare detailed written reports, business correspondence, and procedure manuals
Ability to effectively present information and respond to inquiries or complaints from employees, patients and/or their representatives

Job Responsibility

Serves as a liaison and resource for all departments that utilize Pyxis and the department of pharmacy
Monitors departmental expenses, inventory requirements, inventory costs, utilization reports, controlled substances discrepancies, user sign-ons, all troubleshooting, medication refrigerator temperature capture, Pyxis building, movement and reassignment of all Pyxis units, and coordination of Pyxis maintenance between BD/Carefusion Pyxis and Tucson Medical Center
Conducts all training and competency of pharmacy staff, and as needed – nursing staff, in the use of Pyxis
Provides first level support for business in assigned area ensuring that problems are correctly identified and coordinates resolution with the appropriate members of the Information Services department or vendor
Performs system administration and operational support activities by maintaining user accounts in applications, producing reports and running programs within provided guidelines
Assists in all stages of information technology system implementation such as planning, requirements definition, testing and documentation
Sets up new Pyxis automated dispensing machines ensuring isolated units are tied into the network, makes recommendation for medication stocking based on type of unit and number of beds
Participates in appropriate cross functional meetings where Pyxis is a topic or source of business intelligence
Creates and communicates status reports in accordance with department standards
updates documentation consistently

Fulltime

Clinical Data Analyst III

The Clinical Data Analyst III supports Healthcare metrics, quality and process i...

Location

United States , Los Angeles

Salary:

88854.00 - 142166.00 USD / Year

L.A. Care Health Plan

Expiration Date

Until further notice

Requirements

Bachelor's Degree
At least 4 years of experience in designing, developing, generating and analyzing ad hoc/production reports in Healthcare/Managed Care setting
Must be able to apply and/or develop technical specifications for health care measures such as those used by National Committee for Quality Assurance (NCQA), HEDIS, Centers for Medicare and Medicaid Services (CMS), and State
Must demonstrate advanced SQL and/or SAS skills in developing programs and procedures for analytics and quality assurance
Must be able to present data in a format that is appropriate for analysis
Must demonstrate an aptitude in learning and expanding abilities to use new applications with basic training
Must be a self-starter and can multi-task and can take charge of assigned projects
Must be able to make recommendations to the clients that demonstrate strengths and limitations of the organization's ability to meet the request

Job Responsibility

Design, develop and maintain complex ongoing data projects
Design, develop, and generate ad hoc/production reports
Produce automatic, robust, timely and accurate results based on client specifications
Produce complete documentation, QC reports and periodic results as scheduled
Investigate and document organizational data flow and sources
Develop analytical programs, databases, routine procedures using SAS or SQL programming language
Applies subject expertise in evaluating business operations and processes
Consults across business operations, providing mentorship, and contributing specialized knowledge
Provides training, recommends process improvements, and mentors junior level staff
Communicate with stakeholders/clients/collaborators regarding project details and plans

What we offer

Paid Time Off (PTO)
Tuition Reimbursement
Retirement Plans
Medical, Dental and Vision
Wellness Program
Volunteer Time Off (VTO)

Fulltime

Confirmed Clinical Data Analyst

We are looking for a Confirmed Clinical Data Analyst / Biostatistician to conduc...

Location

France , Paris

Salary:

50000.00 - 55000.00 EUR / Year

Implicity

Expiration Date

Until further notice

Requirements

Master's degree in Biostatistics, Statistics, Data Science, or related field (Ph.D. preferred)
Proven experience in Real-World Evidence (RWE) and Advanced Survival Analysis
Proven expertise in working with large-scale administrative claims databases, specifically the French SNDS/PMSI or similar national health data systems
Strong command of survival analysis and causal inference methodologies, with expertise in longitudinal modeling and complex weighting schemes to address selection and confounding biases
Experience in managing complex inclusion/exclusion criteria and mitigating common observational study biases
Strong command of longitudinal data modeling and causal inference techniques to address selection and confounding biases
Ability to design and draft formal Statistical Analysis Plans (SAP) and Statistical Analysis Reports (SAR)
Expert-level skills in SQL and R or Python for advanced statistical computing
Advanced understanding of data manipulation and the ability to define and implement complex inclusion/exclusion criteria
Strong sense of responsibility and rigor in task follow-up, with a proven ability to meet delivery commitments and deadlines

Job Responsibility

Lead the end-to-end biostatistical process, from initial study design and SAP authoring to final SAR reporting
Execute robust statistical analyses on longitudinal datasets, ensuring appropriate methodologies are used to mitigate common observational study biases
Evaluate clinical and healthcare resource utilization metrics to support scientific evidence generation
Provide the statistical foundation for peer-reviewed publications and high-impact international congress submissions

What we offer

Health care plan: Alan (50% employer)
Luncheon voucher: 9€ (50% employer)
Transport: 50% of your pass OR sustainable mobility pass
Eligible for stock option (BSPCEs) according to the company's existing rules

Fulltime

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Clinical Data Analyst

Job Description

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