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

New

Senior Regulatory Affairs Specialist

ICON plc is a world-leading healthcare intelligence and clinical research organi...

Location

South Korea , Seoul

Salary:

Not provided

iconplc

Expiration Date

Until further notice

Requirements

Degree in Pharmacy preferred
+3 years of experience in pharmaceutical, medical device or health industry
Experience in regulatory affairs or relevant discipline is preferred
Solid understanding of drug development
Good knowledge of National Drug Regulations and Procedures
English Proficiency
Good communication skill for external and internal interaction
Good computer literacy skills, comfortable working with database

Job Responsibility

Achieve timely & successful product registration in accordance with corporate & local strategies
Collect any information on new regulations and guidelines and share it in local RA team
Ensure compliance with company regulatory policies, regulations and procedures
Design and assess local regulatory plans including new strategic concepts and license opportunities and provide consolidated input on key regulatory development in cross-functional team meeting
Manage all regulatory tasks & projects including attaining, maintaining product licenses and operations licenses for assigned portfolio on behalf of company as required by local regulations
Prepare and submit regulatory applications for assigned portfolio and ensure timely approval
Develop local registration plans in alignment with local business and global regulatory strategy
Monitor progress of submission & coordinate timely responses to all questions from health authorities
Be compliant with Corporate Policies, Regulations & Procedures, in particular implementation of current Company Core Data Sheet (CCDS), Change Review Committee (CRC) and local change control procedures
Management of regulatory submissions to support clinical trial activities

What we offer

Various annual leave entitlements
A range of health insurance offerings to suit you and your family's needs
Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being
Life assurance
Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Fulltime

New

Senior Specialists

Location

India , Ahmedabad

Salary:

Not provided

Baxter

Expiration Date

Until further notice

Requirements

Knowledge of regulations
Scientific knowledge
Project management skills
Manage multiple projects and deadlines
Ability to multitask and prioritize
Interpersonal and communication skills
Negotiation skills
Technical system skills (e.g., word processing, spreadsheets, databases, online research)
Ability to identify compliance risks and escalate when necessary
Bachelor’s degree (or equivalent) in a scientific discipline is required, along with 8-10 years of total experience with a minimum of 2 years of regulatory in a pharmaceutical, medical device, CRO, or similar organization. Candidates with prior regulatory and/or technical expertise in complex drug product characterization and regulatory submissions - such as Iron colloids, peptides, liposomes, or biologics will be more preferable.

Job Responsibility

Under limited supervision responsible for the implementation of global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication of general regulatory requirements in support of licensing of Baxter’s products
Support regulatory activities relating to specific portfolio of global products/projects
With direction, develop and execute regulatory project plans
Identify and elevate key areas of regulatory risk
Maintain regulatory files in a format consistent with requirements
Maintain awareness of regulatory requirements
identify relevant requirements
Participate as an active team member and provide regulatory advice to project teams as required
Respond to questions from regulatory authorities within strict timelines
Compile and submit, in a timely manner, regulatory documents according to regulatory requirements

Fulltime

Select Country

Drug Authorization Specialist

Job Description

Job Responsibility

Requirements

Nice to have

Looking for more opportunities?

Drug Authorization Specialist

Drug Authorization Specialist

Drug Authorization Specialist

Drug Authorization Specialist

Prior Authorization Specialist

Specialist Manufacturing - Drug Product Operations

Drug Substance Quality Assurance Specialist

Senior Regulatory Affairs Specialist

Senior Specialists

Our AI answers in your language