Senior Associate - RWE Innovation Programming Job at Amgen (Hyderabad)

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

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

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

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.
MD/DO with board certification in Cardiac, Spine, Gynecologic, or General Surgery
5+ years of experience in Medical Affairs, medical device, or pharmaceutical industry
Prior experience operating at a principal MSL level, including regional strategy influence
Demonstrated ability to build credibility rapidly with surgeons and OR teams
Deep understanding of Medical Affairs Code of Practice and industry compliance standards
Working knowledge of regulatory and clinical research requirements, including IIR processes
Exceptional communication and presentation skills
High ethical standards, professionalism, and scientific rigor

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
Time-off benefits such as paid holidays, paid time off ranging from 20 to 35 days based on length of service, family and medical leaves of absence, and paid parental leave
Commuting benefits
Employee Discount Program
Employee Assistance Program (EAP)

Fulltime

New

Dishwasher

Our Utility Cleaners play an important role in support of a number of vital hote...

Location

United States

Salary:

19.00 USD / Hour

Marriott Bonvoy

Expiration Date

Until further notice

Requirements

No high school diploma or G.E.D. equivalent.
No related work experience.
No supervisory experience.
None

Job Responsibility

Create a safe workplace
Follow company policies and procedures
Uphold quality standards
Ensure uniform, personal appearance, and communications are professional
Ensure adherence to quality expectations and standards
Develop and maintain positive working relationships with other employees and departments
Support team to reach common goals
Listen and respond appropriately to the concerns of other employees
Report accidents, injuries, and unsafe work conditions to manager
Move, lift, carry, push, pull, and place objects weighing less than or equal to 50 pounds without assistance

Parttime

New

Sr. Embedded Software Engineer

The Senior Embedded Engineer contributes significantly to the development of Myo...

Location

United States , Burlington

Salary:

130000.00 - 140000.00 USD / Year

Myomo

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Computer Science, Engineering or related field
6+ years' demonstrated expertise in embedded firmware for electromechanical devices and software delivery in regulated environments
Strong proficiency in at least one embedded-level programming language (e.g., C/C++), and one application-layer language (e.g., Python, Dart, JavaScript/TypeScript)
Proficiency with Linux, FreeRTOS and real-time or resource-constrained environments
Experience with communication libraries and interface design for BLE, UART, I2C, SPI, and CAN
Familiarity in Agile methodologies and modern DevOps tools (e.g., Git, CI/CD pipelines, Docker, automated testing frameworks)
Strong communication and interpersonal skills

Job Responsibility

Define and maintain software architectures in collaboration with Engineering, IT, and Product Management, prioritizing safety, cybersecurity, reliability, scalability, and maintainability
Design, implement, test and document robust embedded firmware and Linux based software solutions
Review code and technical designs with a focus on quality and long-term maintainability
Translate user needs into robust deliverable solutions in close conjunction with Engineering, Product, Quality, and Clinical
Improve software quality through test-driven development, code standards, and continuous integration practices
Foster an environment of continuous learning, improvement, and technical growth

Fulltime

New

Foreign Trade Zone Manager

Location

United States , Wilton

Salary:

Not provided

ASML

Expiration Date

Until further notice

Requirements

Bachelor degree in business administration, finance, tax / customs or related field is required OR 11+ years of foreign trade zone and customs experience in a manufacturing environment
7+ years of logistics or materials management experience in a manufacturing FTZ environment
Customs Brokers License (CBL) required
Strong knowledge of customs regulations and compliance requirements
Proficiency with the Microsoft office suite, Excel, Word, Powerpoint
Experience with SAP, a requirement
Experience with Thomson Reuters Onesource software a plus
Excellent organizational and record-keeping skills
Strong interpersonal skills and the ability to work with people at all levels within the organization
Ability to work under pressure and meet deadlines

Job Responsibility

Manage the logistical, administrative and compliance activities of the FTZ program together with a team of FTZ coordinators and inventory controller
Ensure timely and accurate submission of entries to Customs and Border Protection (CBP)
Ensure timely and accurate submission of entries to FDA and other governmental agencies as required
Coordinate with cross-sector departments (P&D, manufacturing, engineering & sourcing and Tax & Customs) to optimize & support FTZ operations
Prepare and perform audits and inventory control reports
Troubleshoot and resolve complex logistics issues
Maintain detailed records and ensure compliance with FTZ regulations
Work effectively under pressure to meet daily deadlines
Lead, develop & grow team of employees

Fulltime

New

Technical Support Engineer - HMI

The Customer Support Organization is responsible for the installation, qualifica...

Location

United States , San Jose

Salary:

103125.00 - 154688.00 USD / Year

ASML

Expiration Date

Until further notice

Requirements

Bachelors degree in a technical field
Minimum 5 years' relevant work experience
Minimum 3 years experience diagnosing and troubleshooting HMI or similar capital equipment
Minimum 2 years' experience with stakeholder management and partnering with cross functional teams

Job Responsibility

Research, diagnose, troubleshoot and solve Hardware and Software issues
Follow standard procedures to escalate unresolved Hardware and Software issues to designated internal stakeholders
Prepare accurate and timely reports and ensure proper recording and closure of all issues
Document tool issues, and develop the best-known-method(BKM) for troubleshooting cases
Share experiences to the team and contribute to the BKM system
Support Research & Development projects to improve system performance
Equipment installation based on manufacturing specification
Transfer new product knowledge to Field Service Engineers (1L and 2L)
Supporting on-site introduction of new model machines and/or new platforms to our local customer service team and customer engineers
Manage and support new upgrades or commercial options for new and existing HMI systems

What we offer

Medical
dental
vision
basic life insurance
401k plan
eight (8) hours of vacation leave every month
(13) paid holidays throughout the calendar year

Fulltime

Senior Associate - RWE Innovation Programming

Amgen

Location:
India , Hyderabad

Category:
IT - Software Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 05, 2026

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