Drug Authorization Specialist Job at Daley and Associates (Boston)

Drug Authorization Specialist

We are currently seeking candidates for a Drug Authorization Specialist position...

Location

United States , Boston

Salary:

20.00 - 22.00 USD / Hour

Daley and Associates

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Health Science, Healthcare Administration, or a related field (preferred)
1+ years of relevant experience in healthcare administration, health insurance, medical policy review, nursing, or allied health
Proficiency with the Microsoft Office suite
Experience with Epic is a plus
Strong written and verbal communication skills
Detail-oriented, organized, and capable of handling confidential patient information with professionalism

Job Responsibility

Perform pre-registration of new patients by making and receiving calls to collect and document patient demographics, financial details, and other personal information
Verify patient identification and update insurance or demographic data as needed
Manage referral and authorization information for assigned patients
Communicate with physicians and medical providers to clarify clinical details
Maintain accurate and timely documentation of all daily activities in the hospital information system
Support departmental operations and contribute to a positive patient experience through effective communication and attention to detail

Drug Authorization Specialist

We are currently seeking candidates for a Drug Authorization Specialist position...

Location

United States , Boston

Salary:

20.00 - 21.00 USD / Hour

Daley and Associates

Expiration Date

Until further notice

Requirements

Bachelor’s degree in Health Science, Healthcare Administration, or a related field (preferred)
0–2 years of relevant experience in healthcare administration, health insurance, medical policy review, nursing, or allied health
Proficiency with the Microsoft Office suite
Experience with Epic is a plus
Strong written and verbal communication skills
Detail-oriented, organized, and capable of handling confidential patient information with professionalism

Job Responsibility

Perform pre-registration of new patients by making and receiving calls to collect and document patient demographics, financial details, and other personal information
Verify patient identification and update insurance or demographic data as needed
Manage referral and authorization information for assigned patients
Communicate with physicians and medical providers to clarify clinical details
Maintain accurate and timely documentation of all daily activities in the hospital information system
Support departmental operations and contribute to a positive patient experience through effective communication and attention to detail

Fulltime

Drug Authorization Specialist

Drug Authorization Specialist – Boston, MA. We are seeking candidates for a Drug...

Location

United States , Boston

Salary:

20.00 - 22.00 USD / Hour

Daley and Associates

Expiration Date

Until further notice

Requirements

BS in Health Science / Healthcare-related field of study (Preferred)
0-2 years of relevant work experience, including medical billing, denials, healthcare/business administration, health insurance, medical policy/chart review, nursing, and/or other allied health fields
Strong communication skills
Strong Microsoft Office suite experience
Need to be in the New England area

Job Responsibility

Perform pre-registration of new patients by making/receiving patient calls, collecting and documenting patient demographics, financial, and other relevant personal information
Verify patient identification
Update changes to patient insurance and/or demographic information as needed
Manage referral and authorization information as assigned
Communicate regularly with physicians and other medical providers regarding clinical clarifications
Document daily activities in a timely and accurate manner in the hospital information system

Fulltime

Prior Authorization Specialist

PHIL is looking for a full-time Prior Authorization Specialist - with a focus on...

Location

United States

Salary:

21.00 - 25.00 USD / Hour

PHIL

Expiration Date

Until further notice

Requirements

Proven team player, but can solve problems independently as well
Exceptional written and verbal communication skills
Easily adapt to new system and workflow changes
Demonstrate experience working in prior authorizations, medical insurance billing, and/or health insurance (required)
Working knowledge of ICD-10 codes and prescription drug names (preferred, but not required)
Ability to successfully navigate between multiple systems throughout the course of the workday, this includes but is not limited to operational software and vendor portals
Demonstrate flexibility to perform duties wherever volume deems it necessary
Customer service experience (preferred)
Access to reliable, high-speed internet to meet the needs of remote processing (required)

Job Responsibility

Verifies patient insurance coverage utilizing phone or online resources
Submit prior authorizations to insurance plans in a timely manner via electronic portal
Troubleshoots prior authorization submissions and prescription processing with health care providers utilizing phone or online resources
Verbally assist providers in navigating appeals processing
Ensures all pertinent medical documentation is accurate and present prior to authorization submission
Compiles trends in authorization determinations for client and prescriber education
Document activities appropriately in process notes using our operating system
Work closely with our Customer Support team to ensure the success of patients that are recommended to us by their physician's office

What we offer

Ground floor opportunity with one of the fastest-growing startups in health-tech
Solve a problem that matters: be part of a company that uniquely leverages technology to bring wellness to all of its stakeholders

Parttime

Specialist Manufacturing - Drug Product Operations

Join Amgen’s Mission of Serving Patients. At Amgen, our mission—to serve patient...

Location

United States , Thousand Oaks

Salary:

114990.00 - 139433.00 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
Master’s degree and 2 years of Manufacturing support experience
Bachelor’s degree and 4 years of Manufacturing support experience
Associate’s degree and 8 years of Manufacturing support experience
High school diploma / GED and 10 years of Manufacturing support experience

Job Responsibility

Initiate, revise, and approve controlled manufacturing documents within Amgen’s electronic document management system (CDOCs)
Serve as document author, owner, reviewer, or data verifier
Maintain documentation to accurately reflect operational practices and regulatory requirements
Support implementation of new processes, equipment, and major initiatives within Drug Product operations
Collaborate with Capital, Engineering, Process Development, Quality, and other functions to define requirements and achieve operational readiness
Assist in developing and implementing SOPs, batch records, training, validation, and automation configurations
Analyze manufacturing data and performance metrics to identify trends, deviations, and opportunities for improvement
Develop and implement data-driven solutions to improve yield, reliability, and compliance
Support data monitoring using analytical tools such as Enterprise Data Lake and Spotfire
Support timely investigation and resolution of manufacturing deviations

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

Drug Substance Quality Assurance Specialist

In this vital role within the Plant Quality Assurance organization, the Drug Sub...

Location

United States , Thousand Oaks

Salary:

104287.35 - 141094.65 USD / Year

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree OR Master's degree and 2 years of quality experience OR Bachelor's degree and 4 years of quality experience OR Associate's degree and 8 years of quality experience OR High school diploma / GED and 10 years of quality experience

Job Responsibility

Provides Quality oversight, review, and approval of major deviation investigations, ensuring events are thoroughly investigated, appropriately documented, and resolved in accordance with regulatory requirements and site procedures
Partners with Manufacturing, Facilities & Engineering, Quality Control, and other cross-functional stakeholders to facilitate root cause analyses, risk assessments, corrective and preventive actions (CAPAs), and effectiveness verification activities
Maintains the safety of self and others, actively engages with the Amgen EHSS safety program by reporting unsafe conditions if seen and driving improvements
Observes GMP operations within a clean room environment and providing constructive feedback to staff and managers
Reviews and provides Quality approval for GMP documentation such as revisions to procedures and GMP documents, investigation reports for major deviations, change control records, corrective action / preventive action records, and other GMP records
Identifies and escalates significant quality, compliance, supply, and safety risks to management and supports risk-based decision making
Contribute to and drive digital innovation solutions and applications in cross-functional collaboration
Participates as a QA team member process during regulatory inspections, third party audits, and internal audits
Makes certain the Quality Management System processes are executed in accordance with established procedures
May author and own cGMP documents and reports

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 where possible

Fulltime

Production Specialist IV - Radioactive Waste Characterization Specialist

The Radioactive Waste Characterization Specialist is a technical position that p...

Location

United States , Richland

Salary:

115543.99 - 182530.01 USD / Year

Amentum

Expiration Date

Until further notice

Requirements

High School Diploma or GED
Eight (8) years of experience in areas of radioactive and hazardous waste management under the Resource Conservation and Recovery Act (RCRA), Washington State Department of Ecology (WAC 173-303), and DOE M 435.1
Must be authorized to work and remain in the United States without Amentum visa sponsorship now or in the future
Must be able to complete and pass a pre-employment drug screen and background check which includes verification of employment and education
Must be able to obtain a Department of Energy badge for access to the Hanford Site

Job Responsibility

Support the Waste Treatment Plant Nuclear Safety Quality Culture by emphasizing the values of safety and quality in the performance of work in order to protect self, other personnel, facilities, and the environment
Perform all work in compliance with environmental permits and regulations
Maintain knowledge of radioactive waste management requirements found in DOE M 435.1, Radioactive Waste Management Manual
Maintain knowledge of environmental regulations, RCRA regulations and Washington State Dangerous Waste regulations (WAC 173-303)
Provides technical support services to the Waste Management organization for management of radioactive, chemical, and mixed waste-generating activities
Assists the SME in development and execution of effective radioactive, chemical, and mixed waste characterization strategies
Develops radioactive, chemical, and mixed waste management plans, sampling and analysis plans, data quality objectives, and packaging and disposal pathways
Supports development and maintenance of waste management program documentation, including institutional and activity level procedures
Interfaces with other organizations in support of waste characterization activities and methodologies, including laboratory personnel, Plant Engineering, and Process Engineering organizations
Maintains the lead role in providing detailed and accurate radioactive, chemical, and mixed waste characterization data for waste disposal

What we offer

Health, dental, and vision insurance
Paid time off and holidays
Retirement benefits (including 401(k) matching)
Educational reimbursement
Parental leave
Employee stock purchase plan
Tax-saving options
Disability and life insurance
Pet insurance

Fulltime

Remote Bilingual Patient Caseworker

Are you looking for the chance to work 100% from home while utilizing your organ...

Location

Canada , Gatineau

Salary:

52000.00 - 58000.00 CAD / Year ▼

Randstad

Expiration Date

August 06, 2026

Requirements

2+ years of recent experience (within the last 7 years) as a Patient Caseworker, Pharma Reimbursement Specialist, Patient Coordinator, or Patient Care Specialist
5/5 Bilingualism (English/French, oral and written)
Legal eligibility to work full-time in Canada
Experience with CRM systems (such as Salesforce) and Microsoft Office
Reside in Quebec or New Brunswick

Job Responsibility

Coordinate and manage all aspects required to obtain prescription drug coverage for patients
Navigate complex lobbying processes, investigate financial options, manage benefit investigations, and handle special authorizations and appeal requests
Implement call-centre programs providing telephone support to patients, healthcare professionals, and funding bodies regarding funding and access issues
Act as a critical liaison between patients, pharmacies, insurance companies, and physicians' offices to maximize reimbursement solutions and ensure timely medication access
Administer case-management protocols including data collection, ongoing patient follow-up, therapy disruption monitoring, and mandatory adverse event reporting
Accurately document every activity and interaction in the program-specific CRM database and coordinate all related paperwork for insurance and federal funding submissions

What we offer

Permanent & Remote: 100% Work-From-Home permanent opportunity
Day-1 Financial Security: Registered Savings Plan (RSP) with an immediate company match starting on Day 1, plus access to a company stock purchase program
Day-1 Comprehensive Benefits: Immediate access to full medical, dental, and vision care packages
Paid Time Off: 3 weeks of paid vacation, plus designated paid sick and wellness days
Bonus & Salary Growth: Annual performance bonus potential paired with an annual merit review process for salary increases
Wellness & Family Support: Extensive programs focusing on physical, emotional, financial, and social wellness (including backup dependent care, adoption assistance, infertility coverage, family building support, behavioral health solutions, and paid parental/caregiver leave)
Equipment Provided: Home office hardware and equipment are provided as per company policy
Great Work-Life Balance: Monday-Friday schedules

Fulltime

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Drug Authorization Specialist

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