Observational Research Manager Job at Amgen (Seoul)

Epidemiology Analyst

Do you want an exciting position working with multiple teams to generate real wo...

Location

India , Hyderabad

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Master's degree with 8 to 13 years of experience
Strong knowledge of observational research methodology
Excellent communication skills
Attention to detail
Ability to work across various therapeutic areas and regions
Experience in the design, execution, and analysis of observational research studies within Pharmaceutical or Public Health setting
Advanced expertise in medical codelist construction, maintenance, and quality assurance across standard clinical coding systems (e.g., ICD, MedDRA, SNOMED)
Experience in research to support drug development
Experience working with secondary data systems, including administrative claims, EMR, registries
Experience in observational research project planning and management

Job Responsibility

Contribute to global observational research activities for CfOR in support of drug development, registration, and commercialization across Amgen’s portfolio of products
Contribute to the implementation and conduct of observational studies to support the product lifecycle using real world databases and analytics platforms (e.g., Atlas, Aetion, and other internal/external RWD tools)
Develop, review, and maintain high-quality medical codelists for exposures, outcomes, covariates, and safety endpoints using standard coding systems (e.g., ICD, MedDRA, SNOMED, RxNorm), ensuring clinical validity and regulatory readiness
Partner with study team members to ensure codelists are fit-for-purpose, transparent, and reproducible across studies
Executes/manages descriptive epidemiologic studies to characterize the incidence/prevalence of disease in US, EU, Asia, and emerging market countries
Executes/manages research projects involving the analysis of multiple types of data including medical claims, electronic health records, and prospective observational cohort studies
Provides safety research support across the life cycle of Amgen products, supports the development of risk management plans, and executes pharmacovigilance studies
Conducts literature reviews and prepares research reports and scientific manuscripts
Stays abreast of the latest developments in the field of observational research and drug development
Promotes awareness, understanding, and use of observational research methods

Architectural Project Designer - Interior Specialist

Location

United States

Salary:

Not provided

Architectural Design & Construction, Inc.

Expiration Date

Until further notice

Requirements

Learn to create realistic project schedule: estimate time frame for design development, structural design, construction documents
Manage client expectations: schedule, budget, and project scope
Establish due dates for all finish selections for client
Educate client concerning the process and importance of obtaining selections on schedule
Obtain selections on schedule and before construction starts
Record all selections
Obtain client approval in writing before construction starts
Provide client with regular project status reports throughout the design phase
Coordinate with consultants to meet project requirements
Meet project schedule and budget for design services to maintain profitability

Job Responsibility

Reports to the Principal/Construction Project Manager
Properly communicate information regarding selections to the Principal/Construction Project Manager, Project Architect, Project Manager, and client as appropriate and in a timely manner
Prior to all client meetings, share all information that will be presented to a client in the meeting with the Project Team members
Promote, discuss and offer ADC’s Interior Design services when clients have not selected an Interior Designer for their project
Maintain and enhance client relationship with ADC
Walk client through the selections process
Ensure that they understand the phases of construction
Notify suppliers when ADC clients will visit them, if possible
Provide Construction Manager with selections prior to client sign-off on Final Budget Estimate
Assist the Construction Manager putting the selections out to bid with trade contractors and suppliers

Human Subject Research Coordinator 1

Under the direct supervision of the Clinical Trial Manager with direction from t...

Location

United States of America , Rochester

Salary:

21.36 - 29.90 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor’s degree Required
OR Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program Required
Or equivalent combination of education and experience Required
Fluent in the Spanish language (verbal & written) Preferred
Prior experience as a Phlebotomist Preferred
Word processing and data analysis software Preferred
Knowledge of word processing, spreadsheets, Red Cap and electronic data capture (EDC) software Preferred
Excellent communication skills, strong attention to detail, and strong interpersonal skills Preferred
Ability to work independently and as part of a team Preferred
Association of Clinical Research Professionals (ACRP) upon hire Preferred

Job Responsibility

Recruits, consents, schedules, and conducts research subject visits for observational studies
Meets with Spanish-speaking patients interested in research after their clinical visit to discuss research opportunities
Recruits and consents subjects to assigned research studies
Schedules and facilitates visits, performing study related procedures as outlined in protocol
May perform testing such as cognitive function tests, depending on protocol
Resolves questions and concerns received from study subjects, triaging to Principal Investigator as necessary
Monitors study progress on a continuous basis
Understands, implements, and provides training on most recent study protocol
Assists Spanish-speaking patients with research visit appointment confirmation and transportation facilitation
Manages the regulatory details for assigned research studies and registries

Fulltime

Product Marketing Manager

As a Product Marketing Manager at HPE OpsRamp, you will play a pivotal role in d...

Location

United States , Spring, Texas

Salary:

119500.00 - 275000.00 USD / Year

Hewlett Packard Enterprise

Expiration Date

Until further notice

Requirements

BA or BS in Marketing or related field
MBA preferred
10+ years of product marketing experience in one or more of the following domains: infrastructure monitoring, application performance monitoring (APM), cloud-native observability, or AIOps
strong understanding of hybrid IT environments, observability tools, and AI-driven solutions for IT operations
Proven track record of developing go-to-market strategies and crafting compelling product narratives
Ability to work cross-functionally and build strong relationships with product, sales, and marketing teams
Acknowledged mastery of marketing principles, practices, tactics and tools
Ability to manage advertising/direct marketing/research vendors
In-depth understanding of the industry, offering categories and company offerings/strategy
Strong project and budget management skills

Job Responsibility

Develop clear and compelling product positioning that highlights the value of HPE OpsRamp solutions in infrastructure monitoring, cloud-native observability, and AIOps
Create and maintain messaging frameworks tailored to target personas, industries, and use cases
Define and execute go-to-market strategies for existing and new product offerings
Collaborate with cross-functional teams, including product management, engineering, and sales, to align marketing plans with product roadmaps and business objectives
Produce high-impact marketing collateral, including value propositions, presentations, solution briefs, whitepapers, case studies, and blogs
Partner with demand generation teams to create campaign assets such as landing pages, reports, and webinars
Conduct market research to identify trends, customer pain points, and competitive insights
Translate research findings into actionable recommendations for product positioning and differentiation
Develop sales enablement tools, such as battle cards, product training materials, and objection-handling guides
Partner with sales teams to ensure they are equipped to effectively communicate product value to customers

What we offer

Comprehensive suite of benefits that supports physical, financial and emotional wellbeing
Career development and specific programs catered to helping you reach career goals
Inclusive work environment
Flexibility to manage work and personal needs
Opportunity to work for a company that is a force for good

Fulltime

Observational Research Senior Manager

Your role as an Observational Research Senior Manager will be to lead projects a...

Location

United States , Thousand Oaks

Salary:

165267.00 - 186141.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree and at least 2 years of related research and scientific experience
Master's degree and at least 6 years of related research and scientific experience
Bachelor’s degree and 8 years of data sciences and scientific experience
Associate’s degree and 10 years of data sciences and scientific experience
High school diploma / GED and 12 years of data sciences and scientific experience

Job Responsibility

Develop study proposals using real-world data to address key business questions
Lead the design, completion, and delivery of RWE
Facilitate the dissemination of RWE through key presentations, publications and/or trainings
Collaborate on the development of an integrated evidence generation plan for the product team
Contribute to the development and implementation of innovative analytic methods
Partner with cross-functional colleagues to enhance the use of RWE
Build external partnerships to increase the opportunities to use real-world data
Contribute to CfOR’s mission in progressing innovative epidemiological methods and analytical capabilities

What we offer

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions, group medical, dental and vision coverage, life and disability insurance, and flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible

Fulltime

Clin Research Data Spec II

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

23.06 - 32.29 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 1 year of relevant experience required
Or equivalent combination of education and experience
Skill in completing assignments accurately and with attention to detail required
Ability to understand and follow standard research protocols and procedures required
Ability to process and handle confidential information with discretion required
Commitment to the University’s core values required
Ability to work independently and/or in a collaborative environment required
Understands and follows data integrity standards and processes as outlined in the Code of Federal Regulations (CFR), Good Clinical Practices (GCP) and Good Documentation Practices (GDP) required
Strong interpersonal, communication, and organizational skills required
Highly collaborative, works well in teams required

Job Responsibility

Assumes responsibility for the data management of clinical research protocols
Coordinates with the investigational faculty, clinical trial office staff, and sponsor-designated contacts to resolve data inquiries as needed
Formulates and organizes data entry plans to manage assigned caseloads
Responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to Standard Operating Procedures (SOPs), and all applicable regulations and guidelines to ensure timely, accurate and compliant data reporting
Assists in conducting quality checks for data accuracy with data source records as assigned
Reviews medical records for prospective clinical trial patients in conjunction with study eligibility parameters to assist with enrollment
Partners with the primary point of contact to provide data status reports and ensure protocol data objectives are scheduled appropriately
Manages a workload of studies commensurate to level of experience
Answers data clarifications for each study
Schedules and meets with study monitors and ensures patient cases are ready for each monitor visit and items are addressed after each monitoring visit

Fulltime

Clin Research Data Spec II

As a community, the University of Rochester is defined by a deep commitment to M...

Location

United States of America , Rochester

Salary:

23.06 - 32.29 USD / Hour

University of Rochester

Expiration Date

Until further notice

Requirements

Bachelor's degree and 1 year of relevant experience required
Or equivalent combination of education and experience
Skill in completing assignments accurately and with attention to detail required
Ability to understand and follow standard research protocols and procedures required
Ability to process and handle confidential information with discretion required
Commitment to the University’s core values required
Ability to work independently and/or in a collaborative environment required
Understands and follows data integrity standards and processes as outlined in the Code of Federal Regulations (CFR), Good Clinical Practices (GCP) and Good Documentation Practices (GDP) required
Strong interpersonal, communication, and organizational skills required
Highly collaborative, works well in teams required

Job Responsibility

Assumes responsibility for the data management of clinical research protocols
Coordinates with the investigational faculty, clinical trial office staff, and sponsor-designated contacts to resolve data inquiries as needed
Formulates and organizes data entry plans to manage assigned caseloads
Responsible for the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to Standard Operating Procedures (SOPs), and all applicable regulations and guidelines to ensure timely, accurate and compliant data reporting
Assists in conducting quality checks for data accuracy with data source records as assigned
Reviews medical records for prospective clinical trial patients in conjunction with study eligibility parameters to assist with enrollment
Partners with the primary point of contact to provide data status reports and ensure protocol data objectives are scheduled appropriately
Manages a workload of studies commensurate to level of experience
Answers data clarifications for each study
Schedules and meets with study monitors and ensures patient cases are ready for each monitor visit and items are addressed after each monitoring visit

Fulltime

Administrative Coordinator

Office Management & Operations (35%): Serve as the primary point of contact for ...

Location

United States , Los Angeles

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

High school diploma or equivalent required
bachelor’s degree or equivalent experience preferred
Minimum of two (2) years of administrative experience, preferably in an academic or higher education environment
Strong written and verbal communication skills, including experience preparing reports, correspondence, and executive-level materials
Demonstrated ability to manage multiple priorities, meet deadlines, maintain confidentiality, and exercise sound judgment
Highly developed organizational, customer service, and problem-solving skills
Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint) and experience with databases and enterprise systems
ability to learn new technologies quickly

Job Responsibility

Serve as the primary point of contact for all Department programs, projects, and initiatives
Coordinate and support public relations, outreach, and recruitment activities
Act as Department liaison to internal university departments and external partners
Support faculty, speakers, donors, guests, partners, and administrators through preparation of materials, documentation, and logistical coordination
Maintain confidential records and files in collaboration with the Program Coordinator and Grant & Budget Specialist
Coordinate, supervise, and provide administrative oversight for graduate assistants, interns, and work-study students
support fellows and research associates
Manage day-to-day office operations, including troubleshooting office equipment and developing user guides for software and systems
Purchase office supplies, track inventory, and maintain records of Department assets
Coordinate and manage Department mail distribution and electronic accounts

What we offer

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

Observational Research Manager

Amgen

Location:
South Korea , Seoul

Category:
Research and Development

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
December 18, 2025

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