clinical data analyst

Gardner Health Services

<div><div>Gardner Health Services is currently recruiting to fill a Clinical Quality Data Analyst position. This is a full-time (40 hour/week) position based out of the St. James Health Center located in San Jose, California.
Under the direction of the Data Analytics Manager, the Clinical Quality Data Analyst will be an integral team member assisting Gardner Health Services (GHS) efforts to improve the overall quality of care delivered to our patients, their families, and the community we serve. The Clinical Quality Analyst will focus on reporting and assisting with improvement activities for select reports/grant activities, such as community COVID 19 testing/vaccination efforts, patient satisfaction, empanelment, and Integrated Behavioral Health (IBH) grants.
This position will be responsible for the collection (including data entry as needed), creation, management, and analysis of data related to the aforementioned initiatives and other activities as directed. Additionally, this position will assist the CQI Director in training staff and maintaining patient satisfaction efforts as well as other quality priorities that arise for the organization. This position will use tools and techniques of data analytics, Continuous Quality Improvement (CQI), including process improvement, quality improvement activities, analysis and interpretation of data using computer based registries, software, and health records (NextGen) or similar data collection systems. The Clinical Quality Data Analyst will provide CQI support to line staff, management, and executive leadership.
Applications will be reviewed on a first come, first serve basis. Apply now!
Minimum Qualifications:
The minimum qualifications of the position are listed below. An equivalent combination of education and experience may be considered.<ul> 
<li>
Minimum 3 years of clinical experience.</li><li>
Bachelor&rsquo;s Degree (BA) in Health Informatics, Public Health, Healthcare Administration or other related field; Master&rsquo;s Degree (MA), preferred.</li></ul><ul><li>
Ability to effectively present information/trainings and respond to questions from groups of managers, clients and the general public.</li><li>
Bilingual in Spanish/English, Preferred.</li><li>
Experience in or with a federally qualitied health center (FQHC), community health clinic, or non-profit health center, preferred.</li><li>
Experience with electronic health records (EHR) and population analytic software, Next Gen and i2i Tracks, preferred.</li><li>
Knowledge of principles related to Patient Centered Medical Home (PCMH), Uniform Data System (UDS) meaningful use (MU), Healthcare Effectiveness Data and Information Set (HEDIS) incentive programs, and QI models/tools.</li><li>
Working experience in data reporting, data analysis, and CMS/HRSA/MU/HEDIS data measure sets.</li></ul>
*If selected, other documents and certifications may be required as part of the hiring and credentialing process*
Compensation:
Compensation and level of position placement will be determined based on relevant experience and education.
Patient Care Coordinator: $75,000 - $90,000/annually
PLEASE SEE ATTACHED FOR THE FULL JOB DESCRIPTION
Working at Gardner Health Services
Employees at Gardner Health Services define the meaning of community service. Gardner employees are passionate about helping people in the community of which they are a part. Staff members are deeply valued both by the community in which they serve, their fellow colleagues, and company administration. A strong sense of teamwork, empathy, and dedication exists amongst Gardner staff that truly embodies what health care professionals should be. Gardner Health Services takes tremendous pride in seeing the growth and professional advancement of its employees. Employees enjoy a healthy work/life balance and a commitment to diversity and inclusiveness. Additionally, job security is excellent and has led to longtime retention of Gardner personnel. Whether you are new to the healthcare industry and looking to get exposure to a possible career in healthcare or a seasoned veteran who wants to make an impact in the community, Gardner Health Care has a position for you.
Gardner Health Services offers market competitive salaries and an excellent benefits package for eligible employees, including minimal out-of-pocket expenses for health, dental and vision insurance for an entire family. Also included is 401(K) profit sharing contributions, life insurance, an employee assistance program, annual education reimbursement, and a generous paid time off and holiday leave bank.
Who We Are
Gardner Health Services is a dynamic and progressive company dedicated to providing the best healthcare services with a community-oriented approach. Gardner&rsquo;s mission is to provide high quality, comprehensive medical and mental healthcare, including prevention and education, early intervention, treatment and advocacy services which are affordable, respectful, culturally, linguistically and age appropriate.
Compromised of 10 various clinics with locations in the Bay Area of California stretching from Gilroy to Atherton and focused in the San Jose area, Gardner&rsquo;s services are strategically located to ensure adequate coverage in the region and areas with the highest needs. Gardner provides a full range of medical services including pediatrics, dental and vision care as well as a robust program dedicated to mental and behavioral health. Gardner Health Services and its staff are deeply engrained in the community in which they serve and continually strive to go above and beyond to take care of the community and its members.
Gardner Health Services is an equal opportunity employer</div></div>

Clinical Quality Data Analyst

Accenture

Skill required: Clinical Data Services - Clinical eTMF Management 
Designation: Clinical Data Svs Analyst 
Qualifications:Bachelor of Pharmacy
 
Years of Experience:3 to 5 years
 
About Accenture 
Accenture is a global professional services company with leading capabilities in digital, cloud and security.Combining unmatched experience and specialized skills across more than 40 industries, we offer Strategy and Consulting, Technology and Operations services, and Accenture Song&mdash; all powered by the world&rsquo;s largest network of Advanced Technology and Intelligent Operations centers. Our 699,000 people deliver on the promise of technology and human ingenuity every day, serving clients in more than 120 countries. We embrace the power of change to create value and shared success for our clients, people, shareholders, partners and communities.Visit us at www.accenture.com
 
What would you do? You will be aligned with our Life Sciences R&amp;D vertical. Our services span across the entire life sciences enterprise, from research laboratories, clinical trials support, and regulatory services, to pharmacovigilance and patient services solutions. Employees under this span will be a part of one of the sub-offerings - Clinical, Pharmacovigilance &amp; Regulatory, helping the world&acirc;&euro;&trade;s leading biopharma companies bring their vision to life &acirc;&euro;&ldquo; enabling them to improve outcomes by converging around the patient, connecting scientific expertise with unique insights into the patient experience. The Clinical Data Management team focuses on the collection, integration, and availability of data at appropriate quality and cost. The team is responsible for performing data management activities including discrepancy review, query generation, and resolution. The team is also responsible for creating CRF Completion Guidelines (CCG) and SAE reconciliation guidelines. They help identify and raise protocol deviations in the database, perform edit check validation by creating test cases, write test scripts, and carry out database validation (UAT) against the specified CRF/ECRF. The team also managing clinical data management projects. Strategies, methods and tools used throughout the lifecycle of the clinical trial regulated content. Includes data review and accuracy checks of trial master file table of contents, head quarters, initial full protocol package and amended FPP checklists, end of trial checklists, essential document reconciliation, and clinical study report appendices. 
What are we looking for? &bull;Adaptable and flexible &bull;Ability to perform under pressure &bull;Problem-solving skills &bull;Detail orientation &bull;Ability to establish strong client relationship
 
Roles and Responsibilities: Document Administrators are responsible for carrying out format check of documents requiring eCTD compliance for New Drug Application/Marketing Authorization Submission. The format check ensures that the technical quality of submission documents in eCTD compliant and meets the document format standards (e.g., PDF property checks, good documentation practice and bookmark/hyperlink checks).
 
Bachelor of Pharmacy

Clinical Data Svs Analyst

Boston University

<div>The Epidemiology, Clinical, Health Services, and Outcomes (ECHO) research group in the Pulmonary Center at Boston University is seeking a highly motivated Clinical Research Analyst to join our research team. The analyst will play a central role in in data management, statistical analysis, and dissemination of findings through abstracts, manuscripts, and reports. This individual will collaborate with investigators, biostatisticians, and project staff (both internal and external to Boston University) to ensure high-quality data collection, analysis, and reporting. This position is ideal for a candidate who is detail-oriented, thrives in a team-based academic environment, and is interested in pursuing a long-term career in research, medicine, public health, or data science. The candidate must have a strong track record of having worked on prior clinical research wrangling/cleaning large clinical datasets, and have references that can attest that the candidate can:

(1) complete tasks in an efficient, timely manner, (2) communicate both progress and obstacles to the primary investigator, and (3) independently identify and troubleshoot errors in programming. 
 
 
Required Skills 
A letter of recommendation and a sample of analytic code (ideally reflecting medical research experience) is required for consideration

Masters degree in Biostatistics or Data Science. 1-3 years of experience in clinical/health services research; prior experience with healthcare datasets is required, as well as a demonstrated ability to apply new analytic methods. Demonstrated proficiency in statistical software (R or Python; SAS familiarity a plus). Demonstrated ability to manage and analyze large relational data sets in a cloud-based environment, with attention to detail. Excellent written and verbal communication skills, with prior experience contributing to manuscripts or reports preferred. Ability to work independently as well as collaboratively in a team environment to meet deadlines. Familiarity with IRB processes, HIPAA regulations, and NIH-funded research. 


We are an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, natural or protective hairstyle, religion, sex, age, national origin, physical or mental disability, sexual orientation, gender identity, genetic information, military service, pregnancy or pregnancy-related condition, or because of marital, parental, or veteran status. We are a VEVRAA Federal Contractor.</div>

CLINICAL RESEARCH ANALYST, School of Medicine, Pulmonary Center

Novotech

<div>About The Role:
The Clinical Lead Analyst (CLA) works collaboratively with Clinical Lead in managing clinical delivery of the project, by closely monitoring the clinical deliverables, project performance &amp; schedule, compliance, risks, quality of the project.
 Minimum Qualifications &amp; Experience:
<ul><li>Requires minimum of 3 years of work experience, with minimum 1.5 years of relevant experience in a clinical research organization or equivalent role.
</li><li>Basic knowledge of applicable research and regulatory requirements, i.e. International Conference on Harmonization - Good Clinical Practice and relevant local laws, regulations, and guidelines.
</li><li>Knowledge of Microsoft Applications including but not limited to Microsoft Excel, Word and PowerPoint.
</li><li>Exposure to basic data analysis required for projects during start-up, maintenance and close outs.
</li>Certification course in Clinical Research will be an added advantage. 
<li>
</li></ul>Responsibilities:
<ul><li>CLA provides analytics, reports, status update, risk alerts and required mitigation recommendations to the Clinical Lead and rest of the clinical team throughout the lifecycle of the project.
</li><li>CLA supports the Clinical Lead with tools to ensure efficient oversight of clinical deliverables of a project and to ensure adherence to project scope (clinical), protocol, SOPs, applicable regulations, and study plans (CMAP, PD management plan, recruitment plan, IQRMP, IP management, etc.) focusing on applications, analytics, therapeutics, regional requirements, blinding processes, project milestones, and quality perspectives.
</li><li>Conducts periodic review of project KPIs, shares status/analysis, follows up for open action items in accordance to clinical lead&rsquo;s directions.
</li><li>Monitors site-performance parameters at study level and makes recommendations for timely corrective actions under the guidance of Clinical Lead.
</li><li>Evaluates the quality of study processes (clinical) and supports the Clinical in monitoring quality of conduct of the protocol and adherence to applicable regulations.
</li><li>Establishes and maintains effective project/site-level communications with relevant stakeholders (for clinical) as delegated by Clinical Lead.
</li><li>Ensures compliance on study databases (Clinical Trial Management System (CTMS), Interactive Web Response System (IWRS), Electronic Data Capture (EDC) etc.)
</li><li>Supports Clinical Lead in protocol deviation management.
</li>Performs assigned administrative tasks to support Clinical Lead with project execution. 
<li>
</li></ul>Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
 
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
 
We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.</div>

Clinical Lead Analyst

Global Mission Support Services LLC

We Are Hiring: Healthcare Data AnalystLocation: Nauru Medical Centre, Republic of NauruNauru Medical Centre is seeking a highly skilled and experienced Healthcare Data Analyst to join our healthcare team. The Healthcare Data Analyst will be responsible for creating, maintaining, and analyzing medical databases to support clinical, administrative, and operational needs. This role involves working closely with healthcare providers, IT teams, and hospital administration to ensure data integrity, compliance with healthcare regulations, and the effective use of data for decision-making, research, and patient care improvement. The analyst will also be expected to explore data, identify trends, and provide actionable insights to guide hospital strategy and improve healthcare outcomes.Key Responsibilities<ul><li>Design, develop, and maintain medical/clinical databases and data pipelines.</li><li>Collect, clean, and standardize healthcare data from multiple sources (government and hospital databases, lab results, patient records, billing, etc.).</li><li>Ensure data accuracy, consistency, and compliance with healthcare standards.</li><li>Collaborate with clinicians and administrators to define reporting, research, and analytics needs.</li><li>Explore healthcare data to identify trends, anomalies, and opportunities for improvement.</li><li>Generate dashboards, reports, and visualizations for clinical, operational, and strategic insights.</li><li>Support hospital research projects with data extraction, structuring, statistical analysis, and reporting.</li><li>Conduct data-driven investigations to answer key business and clinical questions.</li><li>Identify opportunities to improve data collection processes and workflows.</li></ul>Qualifications<ul><li>Bachelor&rsquo;s or Master&rsquo;s degree in Health Informatics, Data Science, Statistics, Computer Science, or related field.</li><li>Experience with healthcare data management, EMR/EHR systems, or medical coding (ICD, CPT, SNOMED).</li><li>Proficiency in SQL and database management.</li><li>Strong skills in data analysis and statistical tools (Excel, Python, R, or similar).</li><li>Experience with BI tools (Power BI, Tableau, etc.) is a plus.</li><li>Knowledge of healthcare data standards and compliance requirements.</li><li>Strong problem-solving and research skills, with the ability to uncover insights from complex datasets.</li><li>Excellent communication skills to work effectively with both technical and non-technical stakeholders.</li></ul>What We Offer:<ul><li>Competitive tax-free salary</li><li>Free accommodation and meals</li><li>12-month contract with possibility of extension</li><li>30 days paid annual leave</li><li>Round-trip airfare</li><li>A unique professional and personal experience in an island healthcare system</li></ul>Apply Now:Submit your CV and supporting documents to talent@gmss.ltdJob Types: Full-time, Contract Contract length: 12 months

Health Care Data Analyst

<div>About The Role:
The Senior Clinical Lead Analyst (CLA) works collaboratively with Clinical Lead in managing clinical delivery of the project, by closely monitoring the clinical deliverables, project performance &amp; schedule, compliance, risks, quality of the project.
Minimum Qualifications &amp; Experience:
<ul><li>Requires minimum of 5 years of work experience, with minimum 3 years of relevant experience in a clinical research organization or equivalent role.
</li><li>Basic knowledge of applicable research and regulatory requirements, i.e. International Conference on Harmonization - Good Clinical Practice and relevant local laws, regulations, and guidelines.
</li><li>Knowledge of Microsoft Applications including but not limited to Microsoft Excel, Word and PowerPoint.
</li><li>Exposure to basic data analysis required for projects during start-up, maintenance and close outs.
</li><li>Certification course in Clinical Research will be an added advantage.
 </li></ul>Responsibilities:
<ul><li>SCLA provides analytics, reports, status update, risk alerts and required mitigation recommendations to the Clinical Lead and rest of the clinical team throughout the lifecycle of the project.
</li><li>SCLA supports the Clinical Lead with tools to ensure efficient oversight of clinical deliverables of a project and to ensure adherence to project scope (clinical), protocol, SOPs, applicable regulations, and study plans (CMAP, PD management plan, recruitment plan, IQRMP, IP management, etc.) focusing on applications, analytics, therapeutics, regional requirements, blinding processes, project milestones, and quality perspectives.
</li><li>Conducts periodic review of project KPIs, shares status/analysis, follows up for open action items in accordance to clinical lead&rsquo;s directions.
</li><li>Monitors site-performance parameters at study level and makes recommendations for timely corrective actions under the guidance of Clinical Lead.
</li><li>Evaluates the quality of study processes (clinical) and supports the Clinical in monitoring quality of conduct of the protocol and adherence to applicable regulations.
</li><li>Establishes and maintains effective project/site-level communications with relevant stakeholders (for clinical) as delegated by Clinical Lead.
</li><li>Ensures compliance on study databases (Clinical Trial Management System (CTMS), Interactive Web Response System (IWRS), Electronic Data Capture (EDC) etc.)
</li><li>Supports Clinical Lead in protocol deviation management.
</li>Performs assigned administrative tasks to support Clinical Lead with project execution. 
<li>
</li></ul>Novotech is proud to offer a great workplace. We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect. Our team members are passionate about what we do, but we understand work is only of the things that is important to them. We support our team members with flexible working options, paid parental leave for both parents, flexible leave entitlements, wellness programs and ongoing development programs.
 
We are looking for people who are passionate about working clinical research and biotech, including people who identify as LGBTIQ+, have a disability or have caring responsibilities.
 
We are a Circle Back Initiative Employer and commit to respond to every application. We look forward to contacting you regarding your application.</div>

Senior Clinical Lead Analyst

GluCare

Job Summary: We are seeking a Junior Data Analyst - UAE National - to support our clinical and operational teams by analyzing healthcare-related datasets, creating dashboards, and generating actionable insights. This role is ideal for someone early in their data career with strong technical skills, attention to detail, and a passion for healthcare innovation. Prior marketing experience is not required. Key Responsibilities: <ul> <li>Work with healthcare, operational, and research teams to collect, clean, and analyze datasets from EMR systems, wearable devices, CRM platforms, and internal databases.</li> <li>Build and maintain interactive dashboards and reports using tools such as Power BI, Tableau, or Looker Studio to support clinical decision-making and operational planning.</li> <li>Assist in defining and tracking key performance indicators (KPIs) for departments including Clinical Operations, Patient Affairs, and Research.</li> <li>Perform exploratory data analysis (EDA) to identify trends, anomalies, and opportunities for process improvement.</li> <li>Support senior analysts and data scientists in preparing datasets for research publications and strategic projects.</li> <li>Document data processes and ensure data accuracy, privacy, and integrity across systems.</li> <li>Collaborate cross-functionally to understand data needs and translate them into technical deliverables.</li> <li>Generate routine and ad hoc reports for stakeholders as needed.</li> </ul>

Junior Data Analyst - UAE National (Emirati) only

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