Senior Oncology Specialist Job at Amgen (Gainesville)

Senior Oncology Specialist

In this vital role you will be the liaison to our customers by providing clinica...

Location

United States , Austin

Salary:

158727.00 - 177179.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Bachelor’s degree and 3 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related
Associate degree and 6 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related
High school diploma / GED and 8 years of sales experience and/or clinical experience in healthcare / scientific field that is not sales related

Job Responsibility

Act as the primary customer contact to provide current and comprehensive clinical knowledge of Amgen's products and effectively communicate the clinical and economic benefits of the products to medical professionals
Create and execute on a comprehensive territory plan, which includes delivering branded sales messages, executing planned programs, scheduling and following-up with medical educational programs, and achieving or exceeding sales targets
Utilize your internal and external relationships to service and manage accounts, including ensuring product access, resolving/triage reimbursement issues, and maintaining product contracts
Craft an effective marketing strategy to aid in driving sales
Analyze your business effectiveness of sales activities and territory analysis, as well as develop territory plans with your District Manager
Have the passion for our products to sustain that passion through the entire sales cycle while always building our brand and never losing sight of how we serve patients
Partner with other colleagues to share best practices and be in a state of continuous curiosity and learning to help you grow as a Sr. Oncology Specialist
Leverage your passion for Oncology and disease state awareness, Industry, regulatory and competitive changes to deliver agreed results

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, or for field sales representatives, a sales-based incentive plan
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models, including remote and hybrid work arrangements, where possible

Fulltime

Senior Clinical Research Associate II - FSP

As a Clinical Research Associate (CRA) at Parexel, you act as an integral part t...

Location

Turkey

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Extensive knowledge of clinical trial methodologies, ICH/GCP, Food and Drug Administration (FDA) and local country regulations
Monitoring Experience: Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
Global clinical trial experience
Must be fluent in English and in the native language(s) of the country they will work in
Significant travel (60-80%) within area is required. May require some international travel and some weekend travel
Valid driver’s license and passport required
Demonstrated knowledge of clinical research and development processes and ability to gain command of process details
Demonstrated knowledge of global and local regulatory requirements
Demonstrated understanding of key operational elements of clinical research (e.g., monitoring, data acquisition and cleaning, reporting, etc.)

Job Responsibility

Oversight of Monitoring Responsibilities and Study Conduct
Ensure proper conduct of clinical trials in accordance with the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and client standards to achieve project goals, timelines and quality
Manage assigned operational aspects for implementation of clinical trial activities at assigned investigator sites from site activation through to database lock, ensuring relevant timelines and quality deliverables are met
During study conduct, serve as the primary point of contact for assigned investigator sites. Work in partnership with and/or escalate to the SCP to ensure quality of site delivery
Interface with the study team as needed, facilitate information flow between members of the study team, vendors and assigned investigator sites
Partner with SCP to perform investigator site development, coaching and training of site personnel to ensure ongoing compliance with protocol and the safeguarding of patients
provide protocol training to, and address protocol related questions from the investigator site staff when required, including discussions on known/anticipated operational and clinical trial risks
Attend investigator meeting when required (virtual or F2F). Provide enrollment support and ensure progress by responding to site activation and recruitment issues from investigators. Partner with SCP and the study team to define and support recruitment initiatives at site level
Conduct onsite, remote/electronic monitoring as needed for study site initiation, routine monitoring and study site closure activities and ensure these are conducted accordance to the SMP, Standard Operating Procedures (SOPs) and commensurate with emerging issues and technologies
Monitor site level adverse events (AEs) and serious adverse events (SAEs) and collaborate with the Drug Safety Unit and follow-up with investigators sites, as needed, to bring SAE reports required information to resolution

What we offer

Flexible work arrangements
Career growth and development
Supportive and inclusive environment
Diverse therapeutic areas and project exposure
Advanced Technology

Department Program Specialist I

Provides executive high-level administrative support to the Associate Director o...

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 or equivalent combination of education and experience required
5 years of relevant experience preferred
Strong organizational and time-management skills required
Excellent communication and interpersonal skills, especially regarding high-level sensitive information required
Ability to work collaboratively in a team environment required
Advanced knowledge of the medical center, Wilmot and departmental activities required
Basic proficiency with Microsoft Office Suite and social media platforms required
Strong project management skills, with the ability to manage multiple tasks simultaneously preferred
Proficiency with data analysis tools and software preferred
High-level proofreading/editing skills with attention to grammar, punctuation, spelling, etc. preferred

Job Responsibility

Provides executive high-level administrative support to the Associate Director of Wilmot Cancer Institute for Population Science, Co-Director of the URCC NCORP Research Base, and Director of the URMC PEAK Human Performance Clinical Science Program, and Director of the Wilmot RENEW Program
Helps with direct oversight of Wilmot Cancer Institute operations related to Population Science and the Cancer Prevention and Control Program, as well as the RENEW Clinical Exercise Oncology Program
Helps with direct oversight of operations of the URCC NCORP Research Base and PEAK Human Performance Clinical Science Program
Organizes calendars, schedules events and meetings, and manages commitments prioritizing and delegating as appropriate
Oversee email group lists for various groups
Oversee, submit, and ensure compliance with NIHMS and MyNCBI to ensure publications are compliant with federal regulations
Plan, execute and provide high level meeting support for meetings, compiling data, preparing reports, agenda, and distribution and monitoring of action items and follow-up communications
Assists with grants, proposals, and progress reports
Helps with oversite of financials, compliance forms, and financial sign offs
Procurement card holder

Fulltime

Onc hematology field mas

The MAS role family comprises a variety of medical scientific specialties, such ...

Location

Japan , Tokyo

Salary:

Not provided

Pfizer

Expiration Date

Until further notice

Requirements

4 year university undergraduate degree AND master’s degree in life science
Pharmacists 4-year university graduates with pharmacist license and master’s degree or above or equivalent life science research experience
6–year university graduates with pharmacist license
Nurses with master’s degree or above
Veterinarians
Dentists
MDs
Medical/ pharmaceutical expert knowledge of therapeutic disease area/ products
Ability to communicate appropriately and build good relationship with internal/external stakeholders
Work effectively with teams and across functions by demonstrate Pfizer’s Values & Behaviors and the agility to learn from others

Job Responsibility

Demonstrate medical and scientific leadership and expertise
Provide and exchange medical/ scientific information for/from medical institutions (and other related sources) in the assigned area and from stakeholders
Drive for heightened understanding of the clinical and medical attributes of our products
Maintain the highest scientific standards during in/ external activities
Contribute to the implementation of local medical strategies and life cycle clinical plans for inline and pipeline medicines / vaccines
Make important contributions to decisions of medical strategies for assigned products
Contribute to achieving the department/team goals, and/or participate in cross-organizational projects
Play an active role in supporting members in the team/organization
Develop and execute the medical plan aligned with the medical strategy
Identify unmet medical needs and healthcare disparities in the assigned asset(s) and therapeutic area(s)

Fulltime

New

Strategic Account Executive

Our client, a venture-backed, Series D SaaS company in the HRTech / developer to...

Location

United States

Salary:

100000.00 - 125000.00 USD / Year

80Twenty

Expiration Date

Until further notice

Requirements

5–10 years of B2B SaaS sales experience, ideally in HRTech, EdTech, or adjacent platforms
Strong track record of closing new enterprise business and owning full sales cycles
Experience selling into large, complex organizations
Fortune 500 exposure preferred
Comfortable operating in fast-paced, high-growth or startup-style environments
Excellent communication, negotiation, and stakeholder management skills
Highly organized, customer-focused, and collaborative with a strong sense of ownership

Job Responsibility

Own new business development for large enterprise prospects across North America
Drive outbound prospecting, pipeline generation, and deal execution
Partner cross-functionally with growth, marketing, product, and customer teams
Build relationships with senior leaders across Talent, HR, Engineering, and L&D
Clearly articulate value and navigate complex, multi-stakeholder sales cycles
Maintain accurate pipeline visibility, forecasting, and deal hygiene
Act as the voice of the customer, sharing insights to influence product direction

New

Sr. Manager, Brand and Performance Marketing

We’re partnering with a fast-growing food e-commerce marketplace that connects c...

Location

United States , Manhattan

Salary:

150000.00 - 175000.00 USD / Year

80Twenty

Expiration Date

Until further notice

Requirements

7+ years of experience owning an end-to-end performance marketing channel, ideally Audio, Direct Mail, and/or TV
Strong understanding of Audio, Direct Mail, and/or TV marketing best practices & industry standards across audience targeting, creative, and measurement
Strong analytical skills with an ability to identify trends, make data-driven decisions, and articulate them to executives
Deep familiarity with e-commerce KPIs & funnel metrics, and an ability to recognize trends and uncover insights from ad, creative, and customer data
A strong grasp of ROI, incrementality, and measurement & testing frameworks (A/B tests, holdout tests, etc.)
High level of ownership, attention to detail, and urgency to act on learnings & fix issues

Job Responsibility

Oversee the seven+ figure offline channel marketing budget, making recommendations on allocation across channels
Develop & employ a testing roadmap to improve the incrementality and scale of offline channels
Partner with internal analytics & data science teams to identify customer targeting & optimization opportunities
Collaborate with our in-house & agency creative teams to produce performant ads that balance data-driven insights with an artistic “eye” for what will resonate with customers
Drive efficient results through the integration of new insights, learnings derived from performance analysis, and management of our agency partners
Stay ahead of industry trends and introduce innovative practices to keep their strategy fresh and competitive

What we offer

Comprehensive medical, dental, and vision coverage
HSA & Dependent Care FSA
Flexible paid time off
Breakfast and lunch in office
Monthly food credits + generous employee discount
Growth opportunities with lateral and upward mobility

Fulltime

New

Pharmacy Technician in Training

Thrifty White Pharmacy is seeking out a Pharmacy Technician-in-Training in #055 ...

Location

United States , Hettinger

Salary:

Not provided

Thrifty White

Expiration Date

Until further notice

Requirements

Excellent customer service skills
Attention to detail
Ability to maintain patient confidentiality
At least 18 years of age
High school diploma or equivalent
Currently be or willing to become a certified pharmacy technician per North Dakota state requirements
Willing to commit to completing the training program within the timeline provided
Good attendance and punctuality
Able to maintain flexibility in new or changing work roles
Willing to help anywhere in the store or nearby locations as needed

Job Responsibility

Providing excellent customer service to customers by building loyalty and repeat business
Champions Thrifty White programs to patients such as Ready Refill, Medication Synchronization and HealthyPackRx and assists with enrolling patients
Maintains prescription information to ensure accurate records
Understands and follows Medicare Part B requirements
Troubleshoots any rejected claims or billing issues
Assists customers with Medicare Part D questions
Maintains proper level of nursing home filling procedures
Able to learn and implement new and changing technologies on an ongoing basis

What we offer

Competitive wages
Medical
Dental
Vision
Life insurance
401k
Employee Stock Ownership Plan
Paid holidays and vacations
Store discount for you and your family
Free ASHP/ACPE Accredited Pharmacy Technician-in-Training program

Fulltime

New

Angular Frontend Developer

Location

India

Salary:

Not provided

Bridge Soft Solutions

Expiration Date

Until further notice

Requirements

Deep Angular & TypeScript Knowledge: Proven experience in building and scaling complex, enterprise-level single-page applications (SPAs) using Angular (v10+) and TypeScript. Expertise in reactive programming using RxJS, state management (e.g., NgRx, Akita, or services), and the Angular CLI
Expert-Level Web Standards & Performance: Strong command of modern HTML5, CSS3, and SASS/LESS. Extensive experience with optimizing frontend performance, including lazy loading, change detection strategies, bundle size reduction, Lighthouse auditing, and ensuring a blazing-fast First Contentful Paint (FCP)
Authentication & Authorization: Hands-on experience integrating frontend applications with complex Identity and Access Management (IAM) flows like OAuth 2.0 and OpenID Connect (OIDC). Crucial knowledge includes secure token handling (e.g., refresh tokens, token storage), routing protection
Security Best Practices (Frontend Focus): A security-first mindset with experience in preventing common frontend vulnerabilities, specifically Cross-Site Scripting (XSS), Cross-Site Request Forgery (CSRF), and secure API communication. Deep understanding of the Same-Origin Policy and best practices for securely handling user data in the browser
Unit & Component Testing: Proficiency with testing frameworks like Jasmine and Karma for unit testing services and components. Extensive experience with Cypress or Playwright for robust integration and end-to-end (E2E) testing. Familiarity with component-driven development tools (e.g., Storybook) is a plus
UX/UI Integration & Accessibility: Expert-level ability to translate complex design specifications (Figma/Sketch) into pixel-perfect, highly responsive, and accessible user interfaces (WCAG 2.1). Experience with popular component libraries (e.g., Angular Material, PrimeNG) and building reusable, modular design systems
Years of Exp: 5 - 7 Years

Job Responsibility

Architect and build the core user interface and client-side application logic, focusing on performance, maintainability, and security
Design and implement a scalable state management architecture that ensures data consistency and an exceptional, highly responsive user experience
Write critical, high-performance, and maintainable TypeScript code, setting the standard for the entire frontend codebase
Lead a "Frontend Pod" for 3-4 junior to mid-level developers, fostering a collaborative environment centred on quality and best practices
Conduct thorough code reviews to enforce best practices in coding standards, performance, UI/UX consistency, and accessibility
Mentor junior developers on advanced Angular principles, reactive programming patterns with RxJS, and secure frontend development techniques
Break down complex UI/UX features and technical tasks into manageable stories and sub-tasks for the development team

Fulltime

Senior Oncology Specialist

Amgen

Location:
United States , Gainesville

Category:
Sales

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Nice to have:

Additional Information:

Job Posted:
March 04, 2026

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