1,107 Network Analysis jobs in the United Kingdom
Senior Consultant, HEOR (Evidence Evaluation & Network Meta-analysis)
London, London
Parexel
Posted 16 days ago
Job Viewed
Job Description
**Summary of This Role:-**
This Senior Consultant;
* leads and oversees complex evidence evaluation and network meta-analysis (NMA) projects, ensuring the use of robust methodologies and high-quality outputs.
* provides statistical capabilities and methodological leadership throughout all project stages, from planning to completion.
* leverages his/her expertise in evidence synthesis, systematic review methodologies, and advanced statistical techniques to design, develop, and deliver client solutions.
* applies proficiency in statistical theory, data analysis and interpretation, regression analysis, and various statistical software tools (such as WinBugs, R, Stata, Python, and SAS) to drive project success.
This role requires a Master's or Doctoral Degree in Health Economics, Health Policy, Statistics, Biostatistics, Mathematics, or other related quantitative fields.
**Knowledge and Experience** :
+ Training and extensive experience in health economics, including the conceptualization and development of systematic literature reviews and network meta-analyses (8+ years, ideally in a consultancy environment)
+ Strong basis in fundamental statistical concepts and methods and familiarity with techniques such as the development of predictive equations, survival analysis (including parametric methods), longitudinal data analysis, meta-analysis, mixed treatment comparison, and other hierarchical analysis techniques
+ Familiarity with machine learning techniques and Bayesian statistics is a plus
+ Strong communication (spoken and written) and problem-solving skills, and an ability to learn quickly
+ Ability to communicate effectively, in non-technical terms, with project team members and clients
+ Experience in managing projects and leading/coaching a project team
+ Keen interest in medical research, provision of healthcare, and the pharmaceutical industry
**Skills:**
+ Strong computing skills (MS Office), including MS Excel
+ High analytical ability
+ Excellent scientific, business writing, and presentation skills with close attention to detail
+ Ability to work under pressure to meet multiple and sometimes competing deadlines
+ Exceptional communication skills, both oral and in writing, especially in the relaying of technical information and what is essential and strategic to the client
+ Self-motivation, enthusiasm, ambition, and flexibility
+ Competent in written and spoken English
+ Software: SAS (Base, Stat, Graph, Macro), R, SPSS, STATA, and WinBUGS; Python is a plus
**Education**
+ Master's degree or equivalent in either life science or a quantitative discipline, such as health economics, economics, mathematics, or statistics
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
This Senior Consultant;
* leads and oversees complex evidence evaluation and network meta-analysis (NMA) projects, ensuring the use of robust methodologies and high-quality outputs.
* provides statistical capabilities and methodological leadership throughout all project stages, from planning to completion.
* leverages his/her expertise in evidence synthesis, systematic review methodologies, and advanced statistical techniques to design, develop, and deliver client solutions.
* applies proficiency in statistical theory, data analysis and interpretation, regression analysis, and various statistical software tools (such as WinBugs, R, Stata, Python, and SAS) to drive project success.
This role requires a Master's or Doctoral Degree in Health Economics, Health Policy, Statistics, Biostatistics, Mathematics, or other related quantitative fields.
**Knowledge and Experience** :
+ Training and extensive experience in health economics, including the conceptualization and development of systematic literature reviews and network meta-analyses (8+ years, ideally in a consultancy environment)
+ Strong basis in fundamental statistical concepts and methods and familiarity with techniques such as the development of predictive equations, survival analysis (including parametric methods), longitudinal data analysis, meta-analysis, mixed treatment comparison, and other hierarchical analysis techniques
+ Familiarity with machine learning techniques and Bayesian statistics is a plus
+ Strong communication (spoken and written) and problem-solving skills, and an ability to learn quickly
+ Ability to communicate effectively, in non-technical terms, with project team members and clients
+ Experience in managing projects and leading/coaching a project team
+ Keen interest in medical research, provision of healthcare, and the pharmaceutical industry
**Skills:**
+ Strong computing skills (MS Office), including MS Excel
+ High analytical ability
+ Excellent scientific, business writing, and presentation skills with close attention to detail
+ Ability to work under pressure to meet multiple and sometimes competing deadlines
+ Exceptional communication skills, both oral and in writing, especially in the relaying of technical information and what is essential and strategic to the client
+ Self-motivation, enthusiasm, ambition, and flexibility
+ Competent in written and spoken English
+ Software: SAS (Base, Stat, Graph, Macro), R, SPSS, STATA, and WinBUGS; Python is a plus
**Education**
+ Master's degree or equivalent in either life science or a quantitative discipline, such as health economics, economics, mathematics, or statistics
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
This advertiser has chosen not to accept applicants from your region.
0
Quantitative Literature Lead Investigator - Systematic Review/Network Meta Analysis
ThermoFisher Scientific
Posted 13 days ago
Job Viewed
Job Description
**Work Schedule**
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At PPD, the clinical research business of Thermo Fisher Scientific, we are revolutionizing the way real-world evidence (RWE) is generated and utilized. Our work is critical in ensuring successful market access and product uptake, backed by evidence of safety, effectiveness, and value.
As regulators, health technology assessment (HTA) bodies, payors, patients, and healthcare providers (HCPs) increasingly demand transparency into product benefits and risks, the importance of RWE continues to grow. We apply RWE research at every stage of the product life cycle, from early discovery through post-market, complementing clinical trial data to provide a broader patient representation and more accurate assessments of comparative effectiveness, safety outcomes, and long-term benefits.
Join us in aligning clinical and real-world needs to deliver the right solutions at the right time. Harness the power of real-world data (RWD) to unlock vital insights that inform decision making, enhance patient outcomes, and drive innovation. Be a part of a team that is at the forefront of transforming healthcare through RWE.
**Discover Impactful Work:**
The primary responsibilities of the Senior Research Scientist will be to act as advisor or principal investigator on indirect treatment comparison (ITC) analysis projects, including systematic literature reviews (SLRs). The role will direct, oversee, and have overall responsibility for all aspects of study design and execution. In addition, the position entails providing clients with strategic consultation and advice on how best to address research needs and in working closely with and guide project managers and other research associates in delivering the required studies. The role will independently direct key aspects of ITC, SLR, and other literature-based research projects and manage multiple projects with tasks varying to degree by project.
This role can be remote based across Europe
**A day in the Life:**
+ A Day in the Life:
+ Serve as principal investigator for SLR/NMA projects
+ Design and implement systematic and targeted literature reviews and further analysis.
+ Conceptualize study designs and develop projects protocols.
+ Delegate tasks and monitor progress of delegated project tasks
+ Serve as consultant to other principal investigators or staff on other systematic review projects. **Education, Professional Skills & Experience:**
+ PhD or Master's in health sciences, economics, biology, natural sciences or a related field with 8 or more years relevant systematic literature review (SLR) experience or Bachelor's with extensive relevant SLR experience
+ Proven experience in systematic literature review methods in health economics and/or health services research; experience in indirect treatment comparison analysis would be an advantage, but is not essential **Personal Skills & Competencies:**
+ Demonstrated experience in systematic review (SLR) methods in health economics and/or health services research.
+ Deep understanding of research principles, relevant methodology and practical research implementation.
+ Experience with HTA/regulatory submissions, including National Institute for Health and Care. Excellence, SMC, and other European HTA bodies and the European Medicines Agency
+ Excellent communication skills, including presentation skills.
+ Competent in written and spoken English.
+ Experience in using MS Word, PowerPoint, Excel
+ Review and finalize project deliverables and ensure study findings are valid and reliable.
+ Final responsibility for project budgets, deliverables and timelines; and identify scope expansion and need for amendments
+ Collaborating with colleagues and leveraging skills sets of others within the department
+ Direct other "non-billable" activities (e.g. design conceptual approaches for proposals, oversee or implement process improvements, supervise junior staff, identify and pursue business opportunities within Evidera and bring in new projects).
+ Participate in business development, including input into proposal review, kick-off meetings and bid defense meetings by reviewing key challenges and suggesting solutions.
+ Interact with clients to win new business and identify business leads
+ Support sales (meeting annual target) through methodological excellence (systematic reviews and/or ITCs)
+ Lead interactions with clients in the pharmaceutical and medical device industries.
+ Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to multitask.
+ Provide formal or informal leadership, oversight, mentoring, and guidance to junior staff
+ Act as a guide and mentor to the staff across Evidera locations.
+ Participate in staff recruitment efforts (phone screening, interviewing, attending presentations, etc.)
+ Conform to SOPs and other Evidera requirements
+ Travel (internationally) occasionally, as needed.
**Benefits**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
Standard (Mon-Fri)
**Environmental Conditions**
Office
**Job Description**
At PPD, the clinical research business of Thermo Fisher Scientific, we are revolutionizing the way real-world evidence (RWE) is generated and utilized. Our work is critical in ensuring successful market access and product uptake, backed by evidence of safety, effectiveness, and value.
As regulators, health technology assessment (HTA) bodies, payors, patients, and healthcare providers (HCPs) increasingly demand transparency into product benefits and risks, the importance of RWE continues to grow. We apply RWE research at every stage of the product life cycle, from early discovery through post-market, complementing clinical trial data to provide a broader patient representation and more accurate assessments of comparative effectiveness, safety outcomes, and long-term benefits.
Join us in aligning clinical and real-world needs to deliver the right solutions at the right time. Harness the power of real-world data (RWD) to unlock vital insights that inform decision making, enhance patient outcomes, and drive innovation. Be a part of a team that is at the forefront of transforming healthcare through RWE.
**Discover Impactful Work:**
The primary responsibilities of the Senior Research Scientist will be to act as advisor or principal investigator on indirect treatment comparison (ITC) analysis projects, including systematic literature reviews (SLRs). The role will direct, oversee, and have overall responsibility for all aspects of study design and execution. In addition, the position entails providing clients with strategic consultation and advice on how best to address research needs and in working closely with and guide project managers and other research associates in delivering the required studies. The role will independently direct key aspects of ITC, SLR, and other literature-based research projects and manage multiple projects with tasks varying to degree by project.
This role can be remote based across Europe
**A day in the Life:**
+ A Day in the Life:
+ Serve as principal investigator for SLR/NMA projects
+ Design and implement systematic and targeted literature reviews and further analysis.
+ Conceptualize study designs and develop projects protocols.
+ Delegate tasks and monitor progress of delegated project tasks
+ Serve as consultant to other principal investigators or staff on other systematic review projects. **Education, Professional Skills & Experience:**
+ PhD or Master's in health sciences, economics, biology, natural sciences or a related field with 8 or more years relevant systematic literature review (SLR) experience or Bachelor's with extensive relevant SLR experience
+ Proven experience in systematic literature review methods in health economics and/or health services research; experience in indirect treatment comparison analysis would be an advantage, but is not essential **Personal Skills & Competencies:**
+ Demonstrated experience in systematic review (SLR) methods in health economics and/or health services research.
+ Deep understanding of research principles, relevant methodology and practical research implementation.
+ Experience with HTA/regulatory submissions, including National Institute for Health and Care. Excellence, SMC, and other European HTA bodies and the European Medicines Agency
+ Excellent communication skills, including presentation skills.
+ Competent in written and spoken English.
+ Experience in using MS Word, PowerPoint, Excel
+ Review and finalize project deliverables and ensure study findings are valid and reliable.
+ Final responsibility for project budgets, deliverables and timelines; and identify scope expansion and need for amendments
+ Collaborating with colleagues and leveraging skills sets of others within the department
+ Direct other "non-billable" activities (e.g. design conceptual approaches for proposals, oversee or implement process improvements, supervise junior staff, identify and pursue business opportunities within Evidera and bring in new projects).
+ Participate in business development, including input into proposal review, kick-off meetings and bid defense meetings by reviewing key challenges and suggesting solutions.
+ Interact with clients to win new business and identify business leads
+ Support sales (meeting annual target) through methodological excellence (systematic reviews and/or ITCs)
+ Lead interactions with clients in the pharmaceutical and medical device industries.
+ Performs a wide range of variable tasks as dictated by variable demands and changing conditions with little predictability as to the occurrence. Ability to multitask.
+ Provide formal or informal leadership, oversight, mentoring, and guidance to junior staff
+ Act as a guide and mentor to the staff across Evidera locations.
+ Participate in staff recruitment efforts (phone screening, interviewing, attending presentations, etc.)
+ Conform to SOPs and other Evidera requirements
+ Travel (internationally) occasionally, as needed.
**Benefits**
We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
This advertiser has chosen not to accept applicants from your region.
1
Data Analysis and Validation Associate
Pirbright, South East
CK Group- Science, Clinical and Technical
Posted 14 days ago
Job Viewed
Job Description
CK Group are recruiting for a Data Analysis and Validation Associate to join a global animal health company on a contract basis for 12 months.
Salary:
147.90 per day PAYE
Data Analysis and Validation Associate role:
Your Background :
Company:
Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK.
Location:
This role is based at our clients site near Pirbright.
Apply:
For more information, or to apply for this Data Analysis and Validation Associate role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
Salary:
147.90 per day PAYE
Data Analysis and Validation Associate role:
- Responsible for data analysis, entry and Validation related activities across the Pirbright manufacturing facility, to enable the large scale production of FMD and BTV antigen and finished product in a timely and cost effective manner.
- Analyse production data to identify trends, deviations, and performance metrics.
- Assist in the execution of cleaning validation protocols in line with GMP requirements.
- Bring in SQL / Power BI approaches to improve the site approach to data.
- Support sampling, documentation, and coordination of validation activities.
Your Background :
- GMP experience is essential
- Have a scientific or engineering discipline degree (e.g., Biochemistry, Biotechnology, Chemical Engineering, Pharmaceutical Sciences).
- Understanding of cleaning validation principles and documentation practices.
- Experience with data handling and analytics
- Knowledge of HSE, bio-safety standards, GMP regulations as well as main tools and principles of operational excellence
Company:
Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK.
Location:
This role is based at our clients site near Pirbright.
Apply:
For more information, or to apply for this Data Analysis and Validation Associate role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
This advertiser has chosen not to accept applicants from your region.
2
Data Analysis and Validation Associate
Pirbright, South East
CK Group- Science, Clinical and Technical
Posted 14 days ago
Job Viewed
Job Description
CK Group are recruiting for a Data Analysis and Validation Associate to join a global animal health company on a contract basis for 12 months.
Salary:
147.90 per day PAYE
Data Analysis and Validation Associate role:
Your Background :
Company:
Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK.
Location:
This role is based at our clients site near Pirbright.
Apply:
For more information, or to apply for this Data Analysis and Validation Associate role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
Salary:
147.90 per day PAYE
Data Analysis and Validation Associate role:
- Responsible for data analysis, entry and Validation related activities across the Pirbright manufacturing facility, to enable the large scale production of FMD and BTV antigen and finished product in a timely and cost effective manner.
- Analyse production data to identify trends, deviations, and performance metrics.
- Assist in the execution of cleaning validation protocols in line with GMP requirements.
- Bring in SQL / Power BI approaches to improve the site approach to data.
- Support sampling, documentation, and coordination of validation activities.
Your Background :
- GMP experience is essential
- Have a scientific or engineering discipline degree (e.g., Biochemistry, Biotechnology, Chemical Engineering, Pharmaceutical Sciences).
- Understanding of cleaning validation principles and documentation practices.
- Experience with data handling and analytics
- Knowledge of HSE, bio-safety standards, GMP regulations as well as main tools and principles of operational excellence
Company:
Our client is a leading manufacturer of vaccines, parasiticides and pharmaceuticals to protect animals. They are also one of the fastest growing animal health companies in the UK.
Location:
This role is based at our clients site near Pirbright.
Apply:
For more information, or to apply for this Data Analysis and Validation Associate role, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).
It is essential that applicants hold entitlement to work in the UK
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
INDKA
This advertiser has chosen not to accept applicants from your region.
3
Data Analysis Bootcamp (Hiring Immediately)
N1 2UD Islington, London
ITonlinelearning Recruitment
Posted today
Job Viewed
Job Description
Data Analyst Course Programme Job Guarantee Included Complete online training designed to take you from zero experience to your first data analyst role. Study part-time, build fundamental skills, and get dedicated job placement support until you're hired. Flexible financing options available, with payment plans starting from as low as 142 per month. The Programme Complete this 10-week online training with just 10-15 hours per week of study time. You'll learn industry-standard tools, including Excel, SQL, Python, and Power BI, while building a professional portfolio with workplace projects. The programme includes earning BCS and CompTIA certifications recognised by UK employers, expert tutor support throughout your studies, and dedicated job placement support with CV help, interview preparation, and direct employer introductions. The Outcome 93% of graduates secure data analyst roles within 3 months. Starting salaries: 28,000 38,000 Who This Is For The programme is completely beginner friendly, so no experience needed. Career changers are welcome, and you can study at your own pace. *This programme is available to UK-based learners only. Ready to start earning in data? Limited spaces available. Apply now for the next available cohort.
This advertiser has chosen not to accept applicants from your region.
4
Remote Graduate Trainee - Data Analysis
L1 1AA Liverpool, North West
£25000 annum (pro
WhatJobs
Posted today
Job Viewed
Job Description
Our client is offering an exceptional opportunity for motivated graduates to join their organisation as Remote Graduate Trainees in Data Analysis. This is a fully remote, structured training program designed to equip enthusiastic individuals with the essential skills and knowledge required to excel in the field of data analysis. You will gain hands-on experience working with real-world datasets, learning to extract meaningful insights, and contributing to data-driven decision-making across various business functions.
This program is ideal for recent graduates with a strong quantitative background and a keen interest in data. You will receive comprehensive training in data manipulation, statistical analysis, data visualisation, and relevant software tools such as SQL, Python, and R. Mentorship from experienced data professionals will guide your development, providing practical support and career advice. The role demands a high level of analytical thinking, problem-solving skills, and a meticulous attention to detail. As a remote trainee, you will need to demonstrate strong self-discipline, excellent time management, and effective communication skills to collaborate with your cohort and supervisors. This internship offers a fantastic foundation for a career in data science, business intelligence, or related analytical fields, providing valuable industry experience from the outset.
Key Responsibilities:
This program is ideal for recent graduates with a strong quantitative background and a keen interest in data. You will receive comprehensive training in data manipulation, statistical analysis, data visualisation, and relevant software tools such as SQL, Python, and R. Mentorship from experienced data professionals will guide your development, providing practical support and career advice. The role demands a high level of analytical thinking, problem-solving skills, and a meticulous attention to detail. As a remote trainee, you will need to demonstrate strong self-discipline, excellent time management, and effective communication skills to collaborate with your cohort and supervisors. This internship offers a fantastic foundation for a career in data science, business intelligence, or related analytical fields, providing valuable industry experience from the outset.
Key Responsibilities:
- Assist in collecting, cleaning, and processing large datasets.
- Perform data analysis to identify trends, patterns, and insights.
- Develop data visualisations and reports to communicate findings.
- Support senior analysts in various data-related projects.
- Learn and apply statistical methods and analytical techniques.
- Gain proficiency in data analysis tools and software (SQL, Python, R).
- Collaborate with team members in a remote setting.
- Contribute to documentation and knowledge sharing.
- Participate actively in training sessions and workshops.
- Help to ensure data accuracy and integrity.
- Recent graduate with a degree in a quantitative field (e.g., Mathematics, Statistics, Computer Science, Economics, Engineering).
- Strong analytical and problem-solving abilities.
- Aptitude for working with numbers and data.
- Basic understanding of statistical concepts is beneficial.
- Familiarity with programming languages like Python or R is a plus.
- Excellent written and verbal communication skills.
- Ability to work independently and manage time effectively.
- Strong attention to detail.
- Enthusiasm for learning and developing data analysis skills.
- Access to a reliable internet connection for remote work.
This advertiser has chosen not to accept applicants from your region.
5
Lead Forensic Accountant - Data Analysis
EH1 1 Edinburgh, Scotland
£70000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a prominent forensic accounting and litigation support firm, is seeking an experienced Lead Forensic Accountant with a strong focus on data analysis to join their fully remote team. This exciting role allows you to leverage advanced analytical techniques and technology to investigate financial fraud, disputes, and irregularities from anywhere in the UK. You will be a key player in unearthing critical financial evidence and providing expert insights to legal teams and corporate clients, all while enjoying the flexibility of remote work.
The Lead Forensic Accountant will be responsible for designing and executing complex data analysis projects to identify patterns, anomalies, and evidence of financial misconduct. This includes data extraction, cleansing, analysis, and visualization using specialized forensic accounting software and tools. You will prepare detailed reports, conduct expert witness testimony, and advise clients on risk mitigation strategies. A deep understanding of accounting principles, fraud schemes, and data analytics methodologies is crucial. Exceptional communication and presentation skills are required to effectively convey complex findings to diverse audiences, including non-technical stakeholders.
Key responsibilities include:
The ideal candidate will hold a professional accounting qualification (e.g., ACA, ACCA, CPA) and possess a minimum of 7 years of experience in forensic accounting, with a significant emphasis on data analysis and digital forensics. Proficiency in data analytics tools and databases is essential. Strong analytical, critical thinking, and problem-solving skills are paramount. Excellent written and verbal communication skills, including experience with expert witness testimony, are required. As this is a fully remote position, candidates must demonstrate strong self-management, organization, and communication skills. The role is technically affiliated with our office in Edinburgh, Scotland, UK , but performed entirely remotely.
The Lead Forensic Accountant will be responsible for designing and executing complex data analysis projects to identify patterns, anomalies, and evidence of financial misconduct. This includes data extraction, cleansing, analysis, and visualization using specialized forensic accounting software and tools. You will prepare detailed reports, conduct expert witness testimony, and advise clients on risk mitigation strategies. A deep understanding of accounting principles, fraud schemes, and data analytics methodologies is crucial. Exceptional communication and presentation skills are required to effectively convey complex findings to diverse audiences, including non-technical stakeholders.
Key responsibilities include:
- Leading forensic accounting investigations involving large and complex datasets.
- Developing and applying data analytics techniques to detect fraud, money laundering, and other financial irregularities.
- Utilizing forensic accounting software and data visualization tools (e.g., ACL, IDEA, Tableau) for analysis and reporting.
- Performing detailed financial analysis to quantify economic damages and support litigation.
- Extracting, transforming, and analyzing data from various sources, including accounting systems and databases.
- Preparing comprehensive forensic reports and executive summaries.
- Serving as an expert witness in legal proceedings, presenting findings clearly and effectively.
- Collaborating with legal counsel and clients to understand investigative objectives and requirements.
- Mentoring and guiding junior forensic accountants and analysts.
- Staying current with emerging trends in data analytics, cybersecurity, and forensic accounting.
The ideal candidate will hold a professional accounting qualification (e.g., ACA, ACCA, CPA) and possess a minimum of 7 years of experience in forensic accounting, with a significant emphasis on data analysis and digital forensics. Proficiency in data analytics tools and databases is essential. Strong analytical, critical thinking, and problem-solving skills are paramount. Excellent written and verbal communication skills, including experience with expert witness testimony, are required. As this is a fully remote position, candidates must demonstrate strong self-management, organization, and communication skills. The role is technically affiliated with our office in Edinburgh, Scotland, UK , but performed entirely remotely.
This advertiser has chosen not to accept applicants from your region.
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6
Lead Bioinformatician - Genomics Data Analysis
BD7 1AF Bradford, Yorkshire and the Humber
£70000 Annually
WhatJobs
Posted 6 days ago
Job Viewed
Job Description
We are looking for an experienced Lead Bioinformatician to join our cutting-edge research and development team. This is a fully remote position, offering a unique opportunity to contribute to significant scientific advancements from anywhere in the UK. You will be instrumental in designing, developing, and implementing robust bioinformatics pipelines for the analysis of large-scale genomic datasets. Your expertise will drive insights in areas such as disease research, drug discovery, and personalised medicine. Our client is committed to pushing the boundaries of scientific knowledge and seeks individuals who share this passion.
Responsibilities:
Responsibilities:
- Lead the design, development, implementation, and maintenance of scalable bioinformatics pipelines for next-generation sequencing (NGS) data analysis (e.g., WGS, WES, RNA-Seq).
- Analyse and interpret complex genomic and transcriptomic datasets to identify genetic variants, gene expression patterns, and other biologically relevant insights.
- Collaborate closely with biologists, geneticists, clinicians, and computational scientists to define project goals and analytical strategies.
- Develop and apply statistical and machine learning methods for genomic data analysis.
- Ensure the quality, reproducibility, and documentation of all bioinformatics analyses and workflows.
- Stay abreast of the latest advancements in bioinformatics, genomics, and related computational fields.
- Mentor and guide junior bioinformaticians and data analysts.
- Contribute to research proposals, grant applications, and publications.
- Manage data storage, processing, and computational resources effectively.
- Present findings to scientific teams and external collaborators.
- PhD in Bioinformatics, Computational Biology, Genetics, Computer Science, or a related quantitative field.
- Minimum of 6 years of post-doctoral or industry experience in bioinformatics, with a strong focus on genomics data analysis.
- Extensive experience with NGS data processing and analysis pipelines (e.g., BWA, GATK, STAR, Salmon).
- Proficiency in programming languages such as Python, R, and shell scripting.
- Strong knowledge of statistical methods and machine learning techniques applicable to genomics.
- Experience with cloud computing platforms (e.g., AWS, GCP, Azure) and containerization (e.g., Docker, Singularity) is highly desirable.
- Proven ability to manage complex projects and lead a small team.
- Excellent problem-solving, analytical, and critical thinking skills.
- Strong communication and presentation skills, with a track record of publications.
- Ability to work independently and collaboratively in a remote research environment.
This advertiser has chosen not to accept applicants from your region.
7
Data Analysis Engineer - SOX Algorithm
Warwick, West Midlands
Tata Technologies Europe Ltd
Posted 1 day ago
Job Viewed
Job Description
At Tata Technologies we make product development dreams a reality by designing, engineering and validating the products of tomorrow for the worlds leading manufacturers. Due to our continued growth we are now recruiting for a Data Analysis Engineer SOX Algorithm to be based at our customers site in Gaydon .
Our Embedded Systems Solutions department (ESS) encompasses all activities outlined under th.
WHJS1_UKTJ
This advertiser has chosen not to accept applicants from your region.
8
Comprehensive Data Analysis Course (Hiring Immediately)
BB11 9SA Burnley, North West
ITonlinelearning Recruitment
Posted today
Job Viewed
Job Description
Data Analyst Course Programme Job Guarantee Included Complete online training designed to take you from zero experience to your first data analyst role. Study part-time, build fundamental skills, and get dedicated job placement support until you're hired. Flexible financing options available, with payment plans starting from as low as 142 per month. The Programme Complete this 10-week online training with just 10-15 hours per week of study time. You'll learn industry-standard tools, including Excel, SQL, Python, and Power BI, while building a professional portfolio with workplace projects. The programme includes earning BCS and CompTIA certifications recognised by UK employers, expert tutor support throughout your studies, and dedicated job placement support with CV help, interview preparation, and direct employer introductions. The Outcome 93% of graduates secure data analyst roles within 3 months. Starting salaries: 28,000 38,000 Who This Is For The programme is completely beginner friendly, so no experience needed. Career changers are welcome, and you can study at your own pace. *This programme is available to UK-based learners only. Ready to start earning in data? Limited spaces available. Apply now for the next available cohort.
This advertiser has chosen not to accept applicants from your region.
9