clinical research 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

<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

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>Company Description 
Axolabs is a business unit of LGC, and a leading provider of CRO / CDMO capability to the therapeutic oligonucleotide discovery and development industry. Centred out of LGC&rsquo;s site in Kulmbach, Germany, Axolabs works closely with its customers to assist the identification and development of lead candidates with a broad suite of bioinformatics, biology, chemistry, manufacturing and analytical services that support discovery, pre-clinical and clinical trials and scale-up manufacture. With a track record in Nucleic Acid Therapeutics that traces back more than 20 years, Axolabs provides deep knowledge and expertise in the services it provides, working collaboratively and responsively with its clients to assist them in achieving their objectives.
Axolabs facility in Petaluma is focused on manufacturing scale-up and production to cGMP of multigram to kilograms of API for pre-clinical and clinical development. Our site in California has been involved in oligonucleotide synthesis for three decades and established the therapeutics activity in 2019. With around 70 staff and two manufacturing trains, Axolabs offers a flexible manufacturing service out of Petaluma that draws where necessary on our industry and chemical and analytical expertise in Kulmbach. 
Job Description 
This is an Swing Shift: Monday-Thursday (4 x 10 hours, 1pm - 11:30pm).
The QC Associate Scientist brings scientific experience to LGC and is open to both learning more and sharing knowledge with others. You will be part of an ambitious and collaborative team that strives for flawless execution in all tasks.<ul><li>
Setting up instrument sequences, while monitoring analysis and data</li><li>
Performing instrument troubleshooting, maintenance, and reporting of results for timely delivery to internal and external collaborators</li><li>
Coordinating routine and stability analysis, while driving continuous improvement via analytical methodologies</li><li>
Maintaining appropriate quality control processes and procedures to determine accuracy and precision of analysis</li><li>
Demonstrating a familiarity with GMP guidelines 21 CFR Part 210/211 and ICHQ7</li></ul> 

Qualifications 
Minimum Qualifications:<ul><li>
Science degree in Chemistry, Biology or similar with 2 years lab experience in manufacturing</li><li>
Must have strong organic chemistry and/or analytical chemistry knowledge, and proficiency in associated analytical techniques; HPLC, LC-MSMS or GC-MS</li><li>
Proficient in cGMP</li><li>
Solid understanding of analytical manufacturing support</li></ul>
Preferred Qualifications:<ul><li>
Experience in size exclusion, ion exchange, and reverse phase chromatography, KF, FT-IR and NMR techniques preferred</li></ul> 

Additional Information 
What we offer (US based-employees):<ul><li>
Competitive compensation with strong bonus program</li><li>
Comprehensive medical, dental, and vision benefits for employees and dependents</li><li>
FSA/HSA Pre-tax savings plans for health care, childcare, and elder care</li><li>
Deductible Buffer Insurance and Critical Illness Insurance</li><li>
401(k) retirement plan with matching employer contribution</li><li>
Company-paid short- and long- term disability, life insurance, and employee assistance program</li><li>
Pet Insurance for our furry friends</li><li>
Enhanced Parental leave of 8 additional weeks</li><li>
PTO that begins immediately</li><li>
Town Hall monthly meeting onsite/virtual, Cheer program where employees are recognized for outstanding work, Company wide social events and much more!</li></ul>
The typical pay range for this role is:
Minimum: $ 28.12 /Hourly
Maximum: $ 43.19 /Hourly
This range represents the low and high end of the anticipated salary range for the California -based position. The actual base salary will depend on several factors such as: experience, skills, and location.
ABOUT LGC:
LGC is a leading, global life science tools company, providing mission-critical components and solutions into high-growth application areas across the human healthcare and applied market segments. Its high-quality product portfolio is comprised of mission-critical tools for genomic analysis and for quality assurance applications, which are typically embedded and recurring within our customers&rsquo; products and workflows and are valued for their performance, quality, and range.
OUR VALUES<ul><li>
PASSION</li><li>
CURIOSITY</li><li>
INTEGRITY</li><li>
BRILLIANCE</li><li>
RESPECT</li></ul>
EQUAL OPPORTUNITIES
LGC strongly believes that every job applicant and employee should be valued for their individual talents regardless of age, disability, race, color, ethnic or national origin, sex, sexual orientation, gender reassignment, marital or civil partnership, pregnancy or maternity, religion, or belief. Short listing, interviewing and selection will always be carried out without regard to gender, sexual orientation, marital status, color, race, nationality, ethnic or national origins, religion or belief, age, or trade union membership.
For more information about LGC, please visit our website www.lgcgroup.com
#scienceforasaferworld</div>

QC Associate Scientist - CMC Analytical - Swing Shift

Baptist Memorial Health Care

<div>Overview
Job Summary
Analyze, plan, design, maintain, and provide ongoing optimization and support of Baptist OneCare (Epic). Perform workflow assessments, capture business needs and analyze internal business system to determine functional requirements for optimal utilization. Possess clinical, financial, technical or application knowledge and experience. Perform system builds, upgrades, and system enhancements as needed. Support application through all phases of implementation, optimization, and maintenance. Work with cross-functional team and end users to achieve application integration to meet clinical and/or business needs. Exercise discretion and judgment in the performance of original, creative, intellectual work. Incumbent is subject to callback, and on-call as required. Perform other duties as assigned.
Responsibilities<ul>
<li>Facilitates implementation of Baptist OneCare and associated projects to meet organizational objectives and strategies.</li>
<li>Analyzes problems, recommends improvement and develops appropriate action plans utilizing Baptist Management System Tools to promote transformation and ensure successful implementation.</li>
<li>Completes testing of software applications using established standards and protocols.</li>
<li>Provides ongoing support of Epic and other applications under area of responsibility.</li>
<li>Completes assigned goals.</li></ul>
Specifications
Experience
Minimum Required<ul>
<li>Proven combination of experience that demonstrates knowledge of healthcare issues, systems issues, software design and integration. Minimum of five years of relevant experience or combination of experience and education.</li></ul>
Preferred/Desired<ul>
<li>Experience in project management and/or system implementations.</li></ul>
Education
Minimum Required<ul>
<li>Education from an accredited institution or experience as listed. Education of certificate program or two year college degree; Completion of Epic certification within 90 days of completing training.</li></ul>
Preferred/Desired<ul>
<li>Bachelor's degree.</li></ul>
Training
Minimum Required
Preferred/Desired<ul>
<li>Project management or Information Technology training.</li></ul>
Special Skills
Minimum Required<ul>
<li>Proficiency in communicating and performing the techniques of information systems assessment and implementation. Proficiency in communicating and performing Information Technology assessments.</li></ul>
Preferred/Desired
Licensure
Minimum Required
Preferred/Desired</div>

Intermediate Clinical Applications Analyst (Clinical Laboratory, Beaker)

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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