Senior Associate - RWE Application Development Job at Amgen (Hyderabad)

Senior Associate - RWE Regulatory Statistical Programming

Amgen is seeking a dedicated Biostatistical Senior Programmer to join our Center...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
At least four (4) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
Proficiency in SQL programming and SAS or R programming is required
Ability to work effectively within a large, globally distributed team

Job Responsibility

Support a statistical programming team conducting analyses supporting Amgen's Regulatory submission studies and projects
Coordinate with functional leads to prioritize workflow
Provide technical solutions to programming problems within CfOR
Ensure the analysis and presentation of biomedical data is accurate and complete
Adhere to Amgen policies, SOPs and other controlled documents
Write, test, and validate programs in SAS, Databricks, or R to produce analysis datasets and presentation output, to be included in reports for submission to regulatory agencies, publications, and other internal and external communications
Complete programming activities, according to agreed resource and timeline plans
Review key study-related documents produced by other functions, e.g. SAPs, Data Management Plans, etc.
Write and/or review programming plans and analysis dataset specifications
Represent the programming function and participate in multidisciplinary project team meetings

Senior Associate - RWE Obesity Statistical Programming

Amgen is seeking a dedicated Senior Statistical Programmer to join our Center fo...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Computer Science, Statistics, Mathematics, Life Sciences, Economics or other relevant scientific subject
At least four (4) years of relevant statistical programming, systems engineering or application programming experience in a clinical development or life sciences setting
Experience in SQL, and statistical programming using SAS or R

Job Responsibility

Write, test and validate software programs in Unix and Databricks to produce analysis datasets and presentation output such as tables and figures, to be included in reports for submission to regulatory agencies, publications and other communications
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
Manage all programming activities, according to agreed resource and timeline plans
Ensure all programming activities on the project adhere to departmental standards
Write and/or review and approve all programming plans
Write and/or review and approve analysis dataset specifications
Review and approve key study-related documents produced by other functions, e.g. SAPs, CRF, Data Management Plan, etc.
Write, test, validate and execute department-, product- and protocol-level macros and utilities

Associate Director, US Real-World Evidence and Health Outcomes – Oncology Pipeline

This Associate Director role supports the US Pipeline Oncology Director in leadi...

Location

United States , Philadelphia; Durham; Collegeville

Salary:

Not provided

GSK

Expiration Date

Until further notice

Requirements

Master’s degree or PhD in health economics and outcomes research, epidemiology, public health, biostatistics, or a related discipline
At least 1-3 years of experience the pharmaceutical industry and/or managed care, hospital, academic, or healthcare consulting environment with exposure to HEOR/RWE strategy and application
Know-how regarding the US payer/reimbursement and access environment and familiarity with how payer evidence needs inform evidence planning and deliverables (e.g., value evidence strategy, AMCP-style dossier content, budget impact/cost-effectiveness, payer-focused materials), gained through academic, internship, or professional experience
Expertise in RWE and economic evaluation study designs/methods evidenced by publications and/or contributing to study concept sheets and protocols (including clear research questions, endpoints, data source selection, and bias/confounding mitigation), reviewing/authoring key sections of statistical analysis plans and study reports, and ensuring publication/disclosure readiness in accordance with internal SOPs and external requirements
Strong communication and presentation skills, demonstrated by developing and presenting clear, decision-oriented materials (e.g., evidence strategy slides, executive readouts) and summarizing outcomes/next steps for senior audiences
Proven ability to prioritize, pivot, and manage multiple projects simultaneously in a matrix environment

Job Responsibility

Evidence strategy and planning: Co-develop and maintain US RWE & HO plans for 1–2 priority pipeline assets/indications, aligned to US medical, payer, and access needs
translate strategy into actionable workplans, timelines, and resourcing proposals
Study leadership (RWE/HEOR): Own day-to-day leadership for assigned real-world evidence and health outcomes studies (e.g., real-world evidence studies, cost-effectiveness/budget impact analyses, burden of illness, treatment patterns, patient-focused outcomes) including design and execution in partnership with internal functions and external vendors
Cross-functional stakeholder management: Support the US Pipeline Oncology Director in running cross-functional evidence strategy forums and asset-specific meetings by developing agendas/materials, surfacing options, documenting decisions, and tracking actions to closure
Scientific communication and quality: Draft/review project specifications, protocols, statistical analysis plans, study reports, abstracts, posters, and manuscripts
ensure adherence to SOPs and high scientific/operational quality
Trial design input for US relevance: Provide feedback to Clinical Development and cross-functional teams on optimal trial design to ensure enrollment of US-relevant patient populations and collection of endpoints/outcomes that support US stakeholder needs (e.g., health-related quality of life, patient-reported outcomes, resource utilization, and other health outcomes measures)
Internal decision support: Provide RWE & HO input to internal decision-making during development and commercialization planning (e.g., trial design considerations, data gap assessments, value messages, evidence prioritization and sequencing)
Marketed product support : Contribute ~20% effort to US RWE & HO strategy and execution for a marketed product in endometrial and rectal cancer, including data generation planning, cross-functional alignment, and delivery of analyses/publications that support lifecycle evidence needs and value communication
External insight generation: Maintain strong alignment with Field Based Payer Medical Teams and other field stakeholders to obtain customer insights

What we offer

Competitive base salary
Annual bonus based on company performance
Flexible working options available for most roles
Learning and career development
Access to healthcare & wellbeing programmes
Employee recognition programmes

Fulltime

New

Litigation Paralegal

Location

United States , New York

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Prior experience (3+ yrs) working as a Paralegal in a litigation environment
Hands-on knowledge of discovery processes, including document organization and deadline tracking
Familiarity with trial preparation tasks and litigation support activities
Proficiency with case management software and digital file organization tools
Strong written communication skills and careful attention to detail in legal documentation
Ability to manage multiple priorities and maintain accuracy in a deadline-driven setting

Job Responsibility

Coordinate discovery activities by organizing documents, tracking deadlines, and preparing materials for attorney review
Support litigation matters from case intake through resolution by maintaining accurate files and monitoring progress
Maintain and update information in case management software to support efficient matter tracking and reporting
Assist with trial preparation by compiling exhibits, preparing binders, and ensuring required documentation is ready for proceedings
Draft, format, and proofread legal correspondence and case-related documents with a high level of accuracy
Communicate with attorneys, court personnel, and external parties to help move litigation tasks forward on schedule
Conduct file reviews and organize records to improve access to key case information during active matters

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Parttime

New

Janitorial Supervisor

Join Diversified Maintenance! We're committed to delivering exceptional cleaning...

Location

United States , Columbus

Salary:

16.00 USD / Hour

Allied Universal®

Expiration Date

Until further notice

Requirements

High school diploma or equivalent, or a minimum of three (3) years of verifiable work history
Minimum of two (2) years of supervisory experience in the janitorial industry
Attention to detail
Ability to follow instructions effectively

Job Responsibility

Assign tasks to workers, and inspect completed work for conformance to standards
Issues supplies and equipment
Resolve workers' problems or refers matters to the Manager
Perform the duties of workers supervised
Directly supervise the performance outcomes of 2 to 50 janitorial service employees
Assist in training employees
Plan, assign, and direct work
Provide feedback for managers to effectively appraise employee performance
Address customer complaints and resolves problems
Collaborate with employees and perform related duties as a Working Supervisor

What we offer

Weekly Pay

Fulltime

New

Pharmacy Technician

We’re building a world of health around every individual — shaping a more connec...

Location

United States , Philadelphia

Salary:

16.50 - 25.00 USD / Hour

CVS Health

Expiration Date

June 09, 2026

Requirements

Must comply with any state board of pharmacy requirements or laws governing the practice of pharmacy, which includes but is not limited to, age, education, and licensure/certification
If the state board of pharmacy does not address or mandate a minimum age requirement, must be at least 16 years of age
If the state board of pharmacy does not address or mandate a minimum educational requirement, must have a high school diploma or equivalent, or be actively enrolled in high school or high school equivalency program
State-level licensure and national certification requirements vary by state

Job Responsibility

Living our purpose by following all company SOPs at each workstation to help our Pharmacists manage and improve patient health
Following pharmacy workflow procedures at each pharmacy workstation (i.e., production, pick-up, drive-thru, and drop-off) for safe and accurate prescription fulfillment
Contributing to positive patient experiences by showing empathy and genuine care: creating heartfelt and personalized moments while serving patients at pick-up, drive-thru, and over the phone
keeping patients healthy by offering immunizations and other services at the register and over the phone
and demonstrating compassionate care by solving or escalating patient problems
Completing basic inventory activities, as permitted by law, and as directed by the pharmacy leadership team, such as accurately putting away medication deliveries and completing cycle counts, returns-to-stocks, waiting bin inventories, etc.
Contributing to a high-performing team, embracing a growth mindset, and being receptive to feedback
actively seeking opportunities to expand clinical and technical knowledge needed to better assist patients
Remaining flexible for both scheduling and business needs, while contributing to a safe, inclusive, and engaging team dynamic
voluntarily traveling to stores in the market to work shifts as needed by the business

What we offer

dental
vision
wellness resources
employee discounts
access to certain voluntary benefits
other programs

Parttime

New

Customer Service Representative

We want you to join our team as a Customer Service Representative. If you have t...

Location

United States of America , Excelsior

Salary:

14.00 - 15.00 USD / Hour

Circle K

Expiration Date

Until further notice

Requirements

Selling products to customers
Providing excellent customer care
Communication and friendly conversation
Performing at a quick pace while having fun
Working as part of a team to accomplish daily goals
Coming up with great ideas to solve problems
Thinking quickly and offering suggestions

Job Responsibility

You will greet customers, run the register, cashier, make purchase suggestions and sometimes work with our food program
There is never a dull moment as you will be working around the store (inside and out) in many different areas to help maintain our high standards for store appearance and provide fast and friendly service to our customers
Provide regular and predicable onsite attendance
You will interact with many customers daily, all while working with a fun, energetic team accomplishing daily tasks around the store!

What we offer

Medical, Vision, Dental, & Life Insurance/Short & Long Term Disability
Flexible Schedules
Weekly Pay
Weekly Bonus Potential
Large, Stable Employer
Fast Career Opportunities
Work With Fun, Motivated People
Task Variety
Paid Comprehensive Training
401K With a Competitive Company Match

Parttime

New

Data Privacy Attorney

Robert Half is seeking an experienced Privacy Attorney to provide part‑time, int...

Location

United States , New York

Salary:

100.00 - 125.00 USD / Hour

Robert Half

Expiration Date

Until further notice

Requirements

Licensed attorney in any US jurisdiction (Must be active and in good standing)
Senior-level attorney with substantial experience advising on data privacy matters
Demonstrated working knowledge of GDPR, CCPA, and global data protection regimes
Prior in-house experience strongly preferred, with a commercial and business-oriented mindset
Experience supporting institutional or corporate clients (vs. consumer retail environments)
Comfortable operating both hands-on (document drafting, updates) and strategically
Experience advising organizations with international operations
Ability to work independently in a fast-moving environment

Job Responsibility

Provide strategic guidance on global data privacy implications across U.S., UK, Europe, Australia, Canada, and Mexico operations
Update and revise vendor and commercial agreements to incorporate GDPR, CCPA, and other applicable privacy provisions
Review and update privacy notices, policies, and data protection documentation
Analyze business units and workflows to identify data privacy exposure and risk
Support privacy compliance efforts in connection with institutional / B2B customers
Train and advise internal legal teams on evolving data privacy requirements
Contribute to broader privacy and governance frameworks, including intersections with AI and emerging technologies
Assist with internal education and training efforts beyond legal stakeholders, as needed

What we offer

medical
vision
dental
life and disability insurance
401(k) plan

Parttime

Senior Associate - RWE Application Development

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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