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

Vendeur comptoir

En qualité de Vendeur comptoir F/H, vous serez rattaché(e) au responsable du sit...

Location

France , St Jean de Laur

Salary:

1860.00 EUR / Month ▼

Randstad

Expiration Date

July 31, 2026

Requirements

First experience in the building sector and/or in commercial functions
Looking for a versatile position in a human-sized team

Job Responsibility

Greet customers at the counter and on the phone to take orders and provide technical advice in their choice
Identify customer needs and propose suitable products
Receive merchandise to put on the shelves
Prepare and serve customer orders
Work in a team with other storekeepers and salespeople

Fulltime

New

Technical Transition Coordinator

Technical Transition Coordinator - 12-months contract - Brussels 📍 Brussels Ar...

Location

Belgium , Brussels

Salary:

799.00 - 900.00 EUR / Day

Myn

Expiration Date

Until further notice

Requirements

Minimum 15 years of professional IT experience
5+ years' experience within IT infrastructure environments Servers, Networks and Cloud platforms
5+ years working with outsourcing partners
Proven experience managing transitions between service providers
Strong experience coordinating Technical documentation, Runbooks & SOPs and Asset & configuration management
Experience managing complex workstreams using structured plans and tracking tools
Fluent in Dutch or French, plus English (minimum B2)
Available to start no later than 29/06/2026

Job Responsibility

Coordinate end-to-end transition activities and technical handovers
Manage communication between internal teams, vendors, and stakeholders
Oversee knowledge transfer, documentation, and operational readiness
Track risks, issues, and service continuity throughout the transition
Support cutover, testing, go-live, and early-life support activities

Fulltime

New

Account Manager

As an Account Manager at Brkthru, you'll own the day-to-day client relationship ...

Location

United States

Salary:

Not provided

Brkthru

Expiration Date

Until further notice

Requirements

4-6 years in client services, account management, or a client-facing role within digital advertising, media, or a related field
3+ years of experience in digital media, including exposure to paid media and/or programmatic campaigns
Experience managing multiple accounts or campaigns simultaneously in a fast-paced, deadline-driven environment
Experience working with established brands and collaborating across multiple client stakeholders
Own day-to-day client communication with clarity, accountability, and strong follow-through
Connect campaign execution to client goals, KPIs, and measurement approaches
Identify risks, surface opportunities, and communicate recommendations clearly and proactively
Collaborate effectively across Media and internal teams to keep work moving through competing priorities and changing campaign conditions
Maintain strong attention to detail across pacing, delivery, and campaign execution
Translate campaign performance into clear, client-ready insights and next steps

Job Responsibility

Own a book of business, being fully accountable for day-to-day client relationships, ensuring communication is clear, timely, and aligned to business goals
Lead client cadence (weekly calls, agendas, recaps, next steps) and keep both client and internal teams aligned and moving forward
Stay ahead of client needs, risks, and performance challenges, solving issues early, before they impact results or trust
Travel as needed and on-demand based on business necessity to support client relationships, key meetings, and critical moments that benefit from in-person collaboration
Align campaign strategy to client goals, KPIs, and measurement frameworks so performance is evaluated against the right outcomes
Continuously assess pacing and performance, identifying risks, tradeoffs, and optimization opportunities with clarity and urgency
Turn performance data into clear, actionable narratives that help clients understand what's working, what's not, and what to do next
Identify and drive growth opportunities that improve client results and expand the partnership
Partner with Media and cross-functional teams to ensure campaigns launch accurately, execute cleanly, and stay aligned to client expectations
Own campaign setup and QA across insertion orders, assets, tracking, and dashboards, working to avoid gaps and surprises

What we offer

We are a remote and flexible workplace (yay no commuting)
Medical/ Dental/ Vision/ HSA and FSA/ Long Term Disability/ Life and AD&D/ and more…
Company paid Short Term Disability
401k Retirement plan with company match
Pizza Fridays/ Hub Hangouts
Reimbursement of Home Office Expenses
A generous number of Holidays, PTO, and summer Fridays

Fulltime

New

Project Lead Engineer

One of our important clients is currently looking for a Project Lead Engineer, H...

Location

Belgium , Brussels

Salary:

699.00 - 1000.00 EUR / Day

Myn

Expiration Date

Until further notice

Requirements

Master’s degree in Electrical or Electromechanical Engineering (or equivalent experience)
Interest in energy infrastructure and high-voltage projects
Experience in project management and/or site supervision is advantageous
Fluent Dutch is essential
French is a strong plus
Strong organisational and communication skills
Team-oriented with a proactive and solution-focused mindset

Job Responsibility

Lead and coordinate high-voltage cable infrastructure projects
Support technical studies, engineering design, budgeting, and planning
Prepare tender documentation and support procurement activities
Coordinate site execution with contractors, suppliers, and internal stakeholders
Monitor project progress, reporting, and delivery milestones

Select Country

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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