Epidemiologist Job at SRG (London)

New

Senior Research Epidemiologist

We are seeking an experienced Senior Research Epidemiologist to lead and execute...

Location

United States , Seattle

Salary:

142000.00 - 180000.00 USD / Year

Truveta

Expiration Date

Until further notice

Requirements

Master’s or PhD in Epidemiology, Public Health, Biostatistics, Health Policy, or a related field
5+ years of experience in epidemiological, pharmacoepidemiology, or health services research, including leadership or project management responsibilities
Demonstrated experience designing and executing observational studies using real-world data
Strong hands-on experience with statistical programming (R and/or Python)
Experience working with electronic health records (EHRs), claims data, or other real-world healthcare data sources
Proven ability to manage complex, client-facing projects and deliver high-quality outputs under tight timelines
Excellent written and verbal communication skills, including presenting technical concepts to diverse audiences

Job Responsibility

Lead and execute end-to-end epidemiological and real-world evidence studies, ensuring scientific rigor, transparency, and regulatory relevance
Design and oversee study protocols, statistical analysis plans (SAPs), study reports, and manuscripts, including post-authorization safety studies (PASS)
Support or lead studies focused on drug safety in special populations, including pregnant people and neonatal outcomes, where applicable
Ensure research outputs are suitable for regulatory submissions, responses, and post-marketing commitments
Uphold best practices in study conduct, reporting, and Good Pharmacoepidemiology Practices (GPP)
Apply advanced epidemiologic methods across study types
Collaborate closely with analytics and data science teams to review results, assess robustness, and interpret findings
Leverage or interpret outputs from surveillance and signal detection tools, including TreeScan, where applicable
Stay current with evolving regulatory guidance, observational research methods, and industry standards, including expectations for pregnancy safety evaluation
Serve as a primary research point of contact for customers, including life sciences partners and regulatory-focused stakeholders

What we offer

Comprehensive benefits with strong medical, dental and vision insurance plans
401K plan
Professional development & training opportunities for continuous learning
Work/life autonomy via flexible work hours and flexible paid time off
Generous parental leave
Regular team activities (virtual and in-person as soon as we are able)
Additional compensation such as incentive pay and stock options

Fulltime

New

QlikSense Software Developer

The QlikSense Software Developer develops solutions and provides identification/...

Location

United States , Rockville

Salary:

105000.00 - 150000.00 USD / Year

Chickasaw Nation Industries, Inc (CNI)

Expiration Date

Until further notice

Requirements

Must be able to obtain a Public Trust Clearance
A minimum of two (2) years of Qlik Sense experience with of preference for five (5) years of experience building BI applications
Exposure and experience in working on EPLC projects is preferred
Experience FDA technical environments is highly preferred
Bachelor Degree (B.S.) in Information Systems, Computer Science or equivalent and a minimum of nine (9) years of Software development experience

Job Responsibility

Design, develop, and maintain interactive Qlik Sense dashboards and scheduled reports that power safety surveillance across FDA centers
Transform complex adverse event data into actionable business intelligence solutions
Work with Oracle, PostgreSQL, and other database systems to create performant analytics solutions
Perform Qlik Sense based development for generating dashboards, reports, and analytics
Supports software upgrades for QlikSense through dashboard updates and custom development
Implements dashboard refresh mechanisms from multiple sources
Designs, develops, tests, and evaluates software and systems
Oversees projects from analysis through implementation
Coordinates projects between Client Services and IT
Provides weekly or daily technical system set-up status reports

What we offer

Medical
Dental
Vision
401(k)
Family Planning/Fertility Assistance
STD/LTD/Basic Life/AD&D
Legal-Aid Program
Employee Assistance Program (EAP)
Paid Time Off (PTO) – (11) Federal Holidays
Training and Development Opportunities

Fulltime

New

QlikSense Software Developer

The QlikSense Software Developer develops solutions and provides identification/...

Location

United States , Rockville

Salary:

105000.00 - 150000.00 USD / Year

Chickasaw Nation Industries, Inc (CNI)

Expiration Date

Until further notice

Requirements

Must be able to obtain a Public Trust Clearance
A minimum of two (2) years of Qlik Sense experience with of preference for five (5) years of experience building BI applications
Exposure and experience in working on EPLC projects is preferred
Experience FDA technical environments is highly preferred
Bachelor Degree (B.S.) in Information Systems, Computer Science or equivalent and a minimum of nine (9) years of Software development experience

Job Responsibility

Design, develop, and maintain interactive Qlik Sense dashboards and scheduled reports that power safety surveillance across FDA centers
Transform complex adverse event data into actionable business intelligence solutions that support regulatory oversight and public health protection initiatives
Work with Oracle, PostgreSQL, and other database systems to create performant analytics solutions for internal and external stakeholders
Perform Qlik Sense based development for generating dashboards, reports, and analytics
Supports software upgrades for QlikSense through dashboard updates and custom development
Implements dashboard refresh mechanisms from multiple sources through use of manual QVD file refreshes or through database refreshes
Designs, develops, tests, and evaluates software and systems that enable computers to perform their applications, applying principles and techniques of computer science, engineering, and mathematical analysis
Oversees projects from analysis through implementation
Coordinates projects between Client Services and IT as the department and client representative
Provides weekly or daily technical system set-up status reports to team and client, as needed

What we offer

Medical
Dental
Vision
401(k)
Family Planning/Fertility Assistance
STD/LTD/Basic Life/AD&D
Legal-Aid Program
Employee Assistance Program (EAP)
Paid Time Off (PTO) – (11) Federal Holidays
Training and Development Opportunities

Fulltime

Observational Research Manager

Amgen’s Center for Observational Research (CfOR) is seeking a dynamic scientist ...

Location

South Korea , Seoul

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

PhD in pharmacoepidemiology or a related field
Record of publications in observational research
Strong communication and interpersonal skills
Self-motivated with the ability to work independently and collaboratively

Job Responsibility

Leading research based upon secondary data sources of health information (e.g., medical claims, electronic health records, registries)
Design and conduct studies to enhance understanding of disease natural history
Design and conduct studies to evaluate the safety and effectiveness of medicines
Demonstrate technical expertise and creative problem-solving for methodological challenges
Conduct research to highest standards of the profession
Advancing Amgen’s observational research capabilities
Collaborate with Amgen’s global network of epidemiologists and the academic community
Leverage data resources and enhance our analytical capabilities
Engaging with key stakeholders
Coach and promote awareness of the appropriate use of observational research

What we offer

Vast opportunities to learn and move up and across our global organization
Diverse and inclusive community of belonging, where teammates are empowered to bring ideas to the table and act
Generous Total Rewards Plan comprising health, finance and wealth, work/life balance, and career benefits

Principal Rwd Strategy Lead

We are currently looking to recruit an experienced Principal RWD Strategy Lead t...

Location

Multiple , Remote

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

8+ years of industry experience (CRO/Pharma/Data Vendor)
Strong data science/data analytics experience
Strong understanding of the clinical research process and business, medicines and medical device development, healthcare market, and related sectors
Fluent English with a fluency in Chinese an advantage also
Demonstrated ability to apply scientific or real-world data solutions to address clinical or commercial questions and needs
Experienced in budgets and cost evaluation of RWD based solutions
Strong understanding of project management principles
Advanced degree in biomedical informatics, public health, data science, life sciences, or related field required
Excellent oral and written communication skills
Strong customer focus

Job Responsibility

Lead the development and deployment of a RWD strategy for client opportunities and proposals as well as awarded work
Serve as relationship manager and primary point of contact for data providers
Participate in establishment of governance structure for data relationship building
Identify ways in which the partnership can be strengthened
Ensure data partners' needs/expectations are being met
Work with Procurement/LRM to establish/manage MSAs
Handle complex issues related to data applications and/or analysis requirements and how to remedy them
Serve as a SME to the business on the use of the data in clinical research
Identify, assess, and recommend appropriate options to expand access to RWD
Develop working knowledge of RW data sets assigned to strategy leader, keep specifications up-to-date in the data catalog

Power BI - SSRS Developer

The primary objectives of this engagement are to provide business analysis, data...

Location

United States , Exton

Salary:

Not provided

Ocean Blue Solutions

Expiration Date

Until further notice

Requirements

Minimum of 3 years analyzing business needs and processes and formalizing system requirements
Minimum of 3 years analyzing data and utilizing reporting tools such as Microsoft SQL Reporting Services and Power BI
Healthcare industry (focus on health information technology)
Familiarity with laboratory practices (clinical and/or public health laboratory)
Familiarity with standardized nomenclatures (LOINC, SNOMED, etc.) used in communicating test orders and results electronically
Experience in troubleshooting issues in a rapidly changing environment
Proficiency with Microsoft reporting tools such as SQL Server Reporting Services and Power BI
Proficiency with Microsoft Office Suite, SharePoint, and Visio
Ability to analyze business needs and formalize as system requirements
Ability to work as team member and leader

Job Responsibility

Provide analysis and support for LIMS and general BOL data exchange initiatives and existing processes between BOL and internal and external partners
Provide analysis and support for laboratory specific reporting between various health systems and public and private health organizations
Create and maintain business and technical requirements, process, and workflow documentation related to data exchange, reporting, and other laboratory software development projects and initiatives as assigned
Communicate laboratory system or business process needs with multiple business partners to include, IT staff, Epidemiologists, Health program staff, NEDSS technical staff, etc.
Provide onboarding/offboarding support for various laboratory systems
Provide miscellaneous onsite technical assistance to all Divisions within BOL
Assist bioinformatician with IT infrastructure needs
Assist HHSDC technical staff with internal software development and infrastructure projects as needed
Act as liaison between BOL, HHSDC, and external IT vendors
Ensure deliverable compliance with all Commonwealth, DOH, BOL, and HHSDC, standards and procedures

New

Instrument Test Technician

Conducts production testing of assembled flow cytometers and related medical dev...

Location

United States , San Jose

Salary:

27.00 - 30.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Min educational requirement should be AS in electronics
Some experience in Testing mechanicals (i.e. electronics, lasers)
Some experience in manufacturing work setting
Requires an Associate's degree (A.S.) or equivalent from two-year college or technical school
3+ years related experience in a high tech, manufacturing environment
Ability to effectively communicate information and respond to questions both verbally and in writing
Ability to work with mathematical concepts such as probability and statistical inference, and fundamentals of plane and solid geometry
Ability to apply concepts such as fractions, percentages, ratios, and proportions to practical situations
Good mechanical aptitude, dexterity and hand/eye coordination. Must be able to reach, bend and lift 35 lbs on a daily basis
Experienced in the use of: DVM’s, Oscilloscope and general test equipment

Job Responsibility

Conducts production testing of assembled flow cytometers and related medical device products
May integrate systems and conduct a variety of electronic, mechanical, optical, fluidic and electromechanical activities on systems, subassemblies, and parts to ensure unit functions according to specifications
Will be expected to perform system level and subassembly level troubleshooting to determine root cause, and implement correction of assembly or material defects
Responsible for producing quality products on schedule
Performs instrument optimization functions after final assembly: laser alignment, pressure adjustments, electrical adjustments, etc.
Performs final production testing and inspection to ensure products meet performance specifications and standards
Analyzes test results on defective units to determine root cause of failure
Replaces or repairs defective components or assemblies, processes appropriate paperwork, may return unit to assembly for repair
Compares test results with specifications and records test data and plots test results
Generates required documentation to complete the Device History Record (DHR)

Fulltime

New

Quality Control Inspector

The QM Associate Scientist is required to perform testing of various Microorgani...

Location

United States , Sparks

Salary:

15.00 - 19.00 USD / Hour

MillenniumSoft Inc

Expiration Date

Until further notice

Requirements

Experience in handling biological or chemical samples and knowledge of GLP
Basic knowledge in a broad range of laboratory techniques
History of self motivation with a background in biological lab science
Demonstrated verbal and written communication skills in a team environment as well as a desire to work within a team
Capable of readily identifying and analyzing problems
Have basic analytical skills and be familiar with database and statistical software
BS or BA in related field required. Typical degree in Biological Sciences, Chemistry, Molecular, or related field

Job Responsibility

Responsible for Microbiology testing in peptone manufacturing, raw material products, and Final DCM testing as required
Perform testing of various Microorganisms in a Biosafety Level II / III Laboratory with strict adherence to safety policies
Ability to work in a clean room environment and meet validation requirements associated with donning and doffing clean room garments
Responsible for Microbiology testing of prepared media as well as preparing various medias from scratch

Fulltime

Epidemiologist

SRG

Location:
United Kingdom , London

Category:
-

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
January 04, 2026

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Epidemiologist

SRG

Location:United Kingdom , London

Category:-

Contract Type:Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:January 04, 2026

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Location:
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Job Posted:
January 04, 2026