Associate - RWE Innovation Programming Job at Amgen (Hyderabad)

Senior Associate - RWE Innovation Programming

As a Senior Programmer on the Programming Innovations Team, you will play a key ...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, or related field
At least four (4) years of relevant experience in statistical programming, data engineering, or software development in a life sciences or research setting
Proficiency in SAS and/or R, with additional experience in SQL and Python

Job Responsibility

Design, build, and maintain programming solutions and tools that improve efficiency and quality across CfOR’s programming ecosystem
Contribute to the full solution development lifecycle—from requirements gathering and design through testing, deployment, and maintenance
Collaborate with programming teams across CfOR to identify process gaps and prototype scalable solutions using modern programming practices
Support federated innovation—integrating ideas and code contributions from other programming teams into unified, CfOR-wide solutions
Automate repeatable programming tasks and establish standards for modular, reusable code
Leverage AI and machine learning capabilities, including developing and deploying AI agents or copilots, to optimize programming workflows and knowledge sharing
Create and maintain clear, version-controlled documentation, training materials, and user guides to enable sustainable adoption of new tools
Participate in ongoing evaluation and enhancement of tools, ensuring continued performance, security, and relevance
Collaborate with cross-functional partners to align innovations with business needs and technical standards

What we offer

Competitive base salary
Comprehensive Total Rewards plans aligned with industry standards

Senior Associate - RWE Application Development

This crucial role involves generating Real-World Evidence (RWE) to support Amgen...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor's degree with 3-5 Years in Computer Science, Information Technology, or a related field
Proficient in R and R Shiny (Basic)
HTML (Intermediate)
CSS (Intermediate)
JavaScript (Intermediate)
At least four years of relevant career experience in full stack development
Strong working knowledge of HTML, CSS, and JavaScript programming
Scientific and technical excellence
Exceptional oral and written communication skills
Problem-solving abilities

Job Responsibility

Enhance and support existing R Shiny applications with a focus on front-end improvements
Provide support for the Atlas web-based application from the OHDSI community
Develop and implement web solutions using HTML, CSS, and JavaScript
Collaborate with stakeholders to understand their requirements and translate them into technical solutions
Participate in continuous integration and continuous deployment (CI/CD) processes
Manage and optimize data workflows to support efficient data processing and analysis
Maintain clear and effective communication with team members and stakeholders
Provide technical solutions to programming problems within CfOR
Lead and develop technical programming and process improvement initiatives within CfOR
Represent the programming function and participate in multidisciplinary project team meetings

What we offer

Competitive and comprehensive Total Rewards Plans that are aligned with local industry standards

Principal Medical Science Liaison

The Principal Medical Science Liaison (MSL) is a senior, field-based Medical Aff...

Location

United States , Deerfield

Salary:

128000.00 - 176000.00 USD / Year

Baxter

Expiration Date

Until further notice

Requirements

Physician Associate (PA) or Physician (MD/DO) required with a minimum of 3 years of surgical experience in an operating room environment
Ability to travel 70% within the Central U.S.

Job Responsibility

Serve as the senior medical expert for Advanced Surgery technologies, including hemostats, sealants, tissue repair, and emerging surgical innovations
Lead peer-to-peer scientific exchange with surgeons and interdisciplinary healthcare professionals in Cardiac, Spine, Gynecologic, and General Surgery
Translate complex clinical, surgical, and health economic data into actionable medical insights to optimize patient outcomes
Develop and sustain trusted relationships with national, regional, and emerging Surgeon KOLs
Identify, cultivate, and support investigators for Investigator-Initiated Research (IIR) and Baxter-sponsored studies
Capture and communicate voice-of-customer insights to influence clinical evidence strategy and innovation pipelines
Contribute to and help execute regional Medical Affairs strategies, including real-world evidence (RWE) generation and publication planning
Support advisory boards, investigator meetings, and scientific panels
Partner with global and regional teams to support clinical trial feasibility, site identification, and execution
Design and deliver high-impact medical education, including: Medical congress presentations Company-sponsored symposia, Surgical training labs, and mobile lab programs Resident, fellow, and nurse education initiatives

What we offer

Medical and dental coverage that start on day one
Insurance coverage for basic life, accident, short-term and long-term disability, and business travel accident insurance
Employee Stock Purchase Plan (ESPP), with the ability to purchase company stock at a discount
401(k) Retirement Savings Plan (RSP), with options for employee contributions and company matching
Flexible Spending Accounts
Educational assistance programs
Paid holidays
Paid time off ranging from 20 to 35 days based on length of service
Family and medical leaves of absence
Paid parental leave

Fulltime

Senior Manager, Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...

Location

Belgium , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field, with at least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
Ability to work successfully in a matrix and quick paced environment
Ability to multitask priorities to align with program objectives

Job Responsibility

Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives

What we offer

We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development

Medical Director, Global Evidence Generation Lead

The medical Director, evidence generation is responsible for supporting strategi...

Location

Belgium , Mechelen

Salary:

Not provided

Alfasigma

Expiration Date

Until further notice

Requirements

Minimum of 7+ years of experience in evidence generation, clinical development, HEOR, or a related field
At least 5 years of experience in Epidemiology, Health Economics Outcomes Research (HEOR), or/and Health Systems Research
Proven track record of developing and implementing integrated evidence generation plans in the pharmaceutical or biotechnology industry
Experience in design, conduct and oversight of real-world evidence studies ranging from protocol writing to project management oversight and data interpretation and communication
Solid understanding of the cross functional drug development lifecycle and processes (Business Development, clinical trial design, conduct, & endpoint selection, Clinical Operations, Data Management, Biostatistics, and Regulatory)
Demonstrated expertise and experience working with methods for evidence generation using primary and secondary data sources, knowledge of common issues and challenges of implementation, and track-record of successful publications
Demonstrated depth of understanding of observational research methods, regulatory standards, and ability to leverage epidemiologic and data science expertise to meet evolving business needs
Evidence of technical expertise of applying pharmacoepidemiology evidence and insights at the therapy/product level
Ability to explain strengths and limitations of clinical practice datasets — such as electronic health records, claims, clinical data registries, patient generated health data, and other health data sources — in context of designing pharmacoepidemiology study designs
Ability to work successfully in a matrix and quick paced environment

Job Responsibility

Collaborate with cross-functional colleagues to Lead the development and execution of Medical evidence generation strategy and tactics supporting products in development as well as those commercially available, with appropriate prioritization and use of resources ensuring alignment with corporate goals, regional needs, and therapeutic priorities
Oversee the Design and implementation of Integrated Evidence Generation Plans (IEGPs) that incorporate clinical, real-world, and economic data to support product positioning and value demonstration
Scope RWE studies (Regional/National/Academic/Patient/Vendor), selection of new or existing academic (can include: ISR/lIS/NIS)/non-governmental registries (retrospective/prospective), management across various phases from start up, maintenance to final deliverables
Translate (early) trial efficacy to real-world comparative effectiveness as part of early and late phase study planning, identification of subpopulations, and for potential risk-sharing purposes
Design and implement multiple database and/or de novo (e.g. registries) pharmacoepidemiologic studies, as well as literature reviews, intended to provide insight into background epidemiology, disease state regular care, and/or quantify benefits and/or risks potentially associated with Alfasigma products
Project management oversight – ensuring effective design, initiation and implementation of real world evidence studies, while ensuring effective study protocols and plans, managing budget and milestone tracking, and where appropriate contracting with partner organizations
keep abreast on new data and developments in the field, key publications of interest, research methodologies and regulatory standards across the EU and New Markets regions and proactively address HOR strategy changes in collaboration with global and regional teams in anticipation of any trends
Review and provide relevant RWE/HOR inputs to statistical analysis plans and analysis outputs
Understand the legal and compliance environment and drive collaboration with the Legal and Compliance team
Establish metrics to evaluate the effectiveness and impact of evidence generation activities on corporate and product-specific objectives

What we offer

We offer a competitive salary, comprehensive benefits, and extensive opportunities for professional growth and development

New

Multi-Skilled Maintenance Engineer

A global established manufacturing organisation is seeking a Multi-Skilled Maint...

Location

United Kingdom , Coleford

Salary:

38000.00 - 48000.00 GBP / Year

Hunter Selection | B Corp™

Expiration Date

Until further notice

Requirements

Minimum 5 years’ experience in a manufacturing or production environment
Strong experience in fault finding, maintenance systems, and technical drawings
Experience maintaining industrial equipment or automated systems
Experience with Lean, Kaizen, or 5S methodologies
Knowledge of automation/PLC systems
Additional certifications (e.g., IOSH, 18th Edition, FLT, MEWP, PAT)

Job Responsibility

Deliver planned and reactive maintenance across mechanical, electrical, and pneumatic systems
Diagnose faults using structured troubleshooting techniques and technical drawings
Support site facilities maintenance and infrastructure upkeep
Manage spares, tools, and maintenance resources to ensure operational efficiency
Identify and implement continuous improvement initiatives

What we offer

Competitive salary (£38,000 – £48,000)
Company benefits package (pension, holiday, etc.)
Opportunities for training, development, and career progression
Exposure to modern engineering systems and continuous improvement initiatives

Fulltime

New

Learning Support Assistant

Are you ready to be the difference? Role: Learning Support Assistant (LSA). Loca...

Location

United Kingdom , Crawley

Salary:

23000.00 - 25000.00 GBP / Year

Randstad

Expiration Date

July 08, 2026

Requirements

Resilient: thick skin and a warm heart
Intuitive: can read a room and know when a student needs a quiet word of encouragement
Adaptable: comfortable thinking on your feet when a lesson takes an unexpected turn
Reliable: students thrive on consistency
they need someone they can count on every day

Job Responsibility

Empowering Individuals: Working 1:1 or with small groups to break down barriers to learning
Problem Solving: Tailoring classroom materials to help students with SEND click with the curriculum
Mentoring: Helping students manage their emotions and build the social confidence they need to thrive
Collaborating: Working as a key part of a dedicated team to ensure no child is left behind

What we offer

Training and education
Referral Bonus

New

Project Facilitator

A leading manufacturing business in Cheshire is expanding and looking for a Proj...

Location

United Kingdom , Knutsford

Salary:

Not provided

Hunter Selection | B Corp™

Expiration Date

Until further notice

Requirements

3+ years in industry, ideally within an SME or manufacturing environment
Background in food, chemical or bulk-handling sectors is a strong advantage
HNC/HND/Degree in electrical or mechanical engineering is desired

Job Responsibility

Deliver assigned projects on time, to spec and within budget
Act as the key contact for the client
Coordinate internal teams and external suppliers for smooth project delivery
Manage scope, schedule and cost changes with clear documentation
Track progress against plans, budgets and milestones
Escalate risks and issues where needed
Maintain all project documentation

What we offer

Pension
Holidays
Life Assurance
Healthcare
25 Days Holiday
BH

Fulltime

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Associate - RWE Innovation Programming

Job Description

Job Responsibility

Requirements

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