Document Scanner Job at Beacon Hill (Reno)

Opex operator

Our client is seeking enthusiastic Opex Operators to help manage the preparation...

Location

United Kingdom , Swindon

Salary:

12.21 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Strong attention to detail and organisational skills
Ability to work efficiently under pressure
A proactive approach to problem-solving
Team player with excellent communication skills

Job Responsibility

Administration and preparation of medical records and documentation
Efficiently scan documents using Opex scanners, achieving 800+ pages per hour
Escalate errors and queries as needed to maintain quality
Address system and hardware errors promptly
Meet operational performance targets consistently
Perform manual handling of boxes, up to 15Kg

What we offer

Gain valuable experience in a critical sector
Work in a supportive environment that values your contributions

Fulltime

Scanner

We’re looking for a Scanner to join our team in Madison from February – April to...

Location

United States , Madison

Salary:

Not provided

Wegner CPAs

Expiration Date

Until further notice

Requirements

No experience necessary

Job Responsibility

scanning confidential client documents
assist with important document management

Parttime

Configuration Management Specialist

The Configuration Management (CM) Team is responsible for developing, implementi...

Location

United States , Vandenberg SFB

Salary:

115000.00 - 125000.00 USD / Year

Delta Solutions & Strategies

Expiration Date

Until further notice

Requirements

TS/SCI Security Clearance
Minimum 5 years of related experience in configuration management or system documentation
Bachelor’s degree in Information Technology, Systems Engineering, or a related discipline, or equivalent combination of education and experience
ITIL Foundation or equivalent certification preferred
Additional certifications in configuration or data management (e.g., CMII, CMPIC, or DoD-recognized CM programs) desirable
Ability to work with classified and unclassified systems while maintaining compliance with DoD configuration control and data protection standards
Proficiency in configuration management or asset tracking tools such as Xacta, Remedy, ServiceNow, or equivalent
Strong attention to detail and accuracy in technical documentation
Ability to coordinate across multidisciplinary teams including engineering, cybersecurity, logistics, and network operations

Job Responsibility

Maintain comprehensive configuration documentation baselines and process configuration management (CM) change requests
Document and track configuration change board (CCB) meetings
Maintain and update current system configuration documentation using government-approved tools
Maintain configuration documentation for data centers and communications rooms
Maintain configuration documentation for building floor plans and diagrams
Maintain configuration documentation for all phones, printers, and scanners
Maintain configuration documentation for physical and logical network infrastructure architectures
Maintain configuration documentation for software configurations above the standard desktop baseline
Provide informal status reports
Conduct and document monthly configuration audits

Fulltime

Logistics Clerk

We are looking for a detail-oriented Logistics Clerk to join our team in Jamaica...

Location

United States , Jamaica, New York

Salary:

Not provided

Robert Half

Expiration Date

Until further notice

Requirements

Review and verify shipping documents, including invoices and bills of lading, for compliance with regulations
Ensure adherence to company policies and procedures in all aspects of documentation processing
Perform accurate data entry to maintain organized and updated records
Manage physical and digital files systematically for easy retrieval
Collaborate with team members to achieve efficient and positive outcomes
Adapt to shifting priorities and tasks with flexibility and a solution-oriented mindset
Operate office equipment such as copiers and scanners to support document management
Take initiative to exceed job expectations and contribute to organizational success
Work independently to make thoughtful decisions and complete tasks effectively
Monitor and maintain the integrity of shipping and receiving records

Job Responsibility

Review and verify shipping documents, including invoices and bills of lading, for compliance with regulations
Ensure adherence to company policies and procedures in all aspects of documentation processing
Perform accurate data entry to maintain organized and updated records
Manage physical and digital files systematically for easy retrieval
Collaborate with team members to achieve efficient and positive outcomes
Adapt to shifting priorities and tasks with flexibility and a solution-oriented mindset
Operate office equipment such as copiers and scanners to support document management
Take initiative to exceed job expectations and contribute to organizational success
Work independently to make thoughtful decisions and complete tasks effectively
Monitor and maintain the integrity of shipping and receiving records

What we offer

medical, vision, dental, and life and disability insurance
eligible to enroll in our company 401(k) plan

New

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...

Location

United States

Salary:

142100.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
Experience writing, reviewing, or editing protocols and clinical study reports required
Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
Experience writing, reviewing, or editing regulatory briefing books preferred
Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
Ability to interpret and create complex tabular and graphical clinical data presentations
Advanced applied knowledge of basic clinical laboratory tests
Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Job Responsibility

Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives (eligibility may vary based on role)
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Senior Medical Writer

The Senior Medical Writer applies advanced documentation preparation and documen...

Location

United States , San Rafael

Salary:

116000.00 - 159500.00 USD / Year

BioMarin Pharmaceutical

Expiration Date

Until further notice

Requirements

Up to 6 years of as a medical writer in the pharmaceutical industry – OR - at least 10 years of medical or scientific writing experience as a primary job responsibility
Experience writing, reviewing, or editing protocols and clinical study reports required
Experience writing, reviewing, or editing INDs, BLA/NDAs, PBRERs, DSURs, and PAERs highly preferred
Experience writing, reviewing, or editing regulatory briefing books preferred
Advanced applied knowledge of routine document content preparation, including the use of style guides (internal, AMA, CBE, Chicago), medical dictionaries, and guidance documents that prescribe content
Ability to interpret and create complex tabular and graphical clinical data presentations
Advanced applied knowledge of basic clinical laboratory tests
Understanding of the concepts of coding dictionaries (MedDRA, WHO Drug)
Advanced understanding of the drug development process (discovery to market), biostatistical and clinical research concepts, clinical study conduct, clinical study data collection, database management, data integration, and generation of datasets
Intermediate to advanced understanding of scientific concepts integral to nonclinical development, CMC, PK, PD, and antibody detection

Job Responsibility

Applies advanced documentation preparation and document project management skills to assist in the development, drafting, review, editing, and finalization of documents used in conducting clinical studies and reporting clinical study results for regulatory submissions and publications
Drafts and edits documents used in conducting and reporting the results of clinical studies, including protocols, protocol amendments, informed consent forms, and clinical study reports
Drafts and edits documents used in reporting aggregate safety and efficacy information for a molecule, such as investigator’s brochures and periodic safety reports (PBRERs, DSURs, etc.)
Drafts and edits documents used in the preparation of regulatory filings (eg, briefing books, eCTD Module 2/Module 5 clinical or integrated summaries)
Manages study team participation in the preparation of such documents, including calling/running meetings, developing and managing timelines, and managing the document review and comment adjudication processes
Represents Global Medical Writing at cross-functional team meetings (eg, study team, development team, other subteams)
Builds effective partnerships with cross-functional groups to ensure customer/stakeholder needs are met
Provides peer review and editing support for other regulatory documents, such as statistical analysis plans, CRFs, and other study materials
Assists in developing and reviewing standard processes and templates within Global Medical Writing, and may also review/consult on the development of standard processes and templates in other departments
Adheres to departmental procedures and practices and technical and industry standards during all aspects of work

What we offer

Discretionary annual bonus
Discretionary stock-based long-term incentives
Paid time off
Company-sponsored medical, dental, vision, and life insurance plans

Fulltime

Opex Operator

Are you ready to join an exciting opportunity in Swindon? Our client is seeking ...

Location

United Kingdom , Swindon

Salary:

12.21 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Strong attention to detail and organisational skills
Ability to work efficiently under pressure
A proactive approach to problem-solving
Team player with excellent communication skills

Job Responsibility

Administration and preparation of medical records and documentation
Efficiently scan documents using Opex scanners, achieving 800+ pages per hour
Escalate errors and queries as needed to maintain quality
Address system and hardware errors promptly
Meet operational performance targets consistently
Perform manual handling of boxes, up to 15Kg

What we offer

Be part of a dynamic team focused on operational excellence
Gain valuable experience in a critical sector
Work in a supportive environment that values your contributions

Fulltime

Opex operator

Are you ready to join an exciting opportunity in Swindon? Our client is seeking ...

Location

United Kingdom , Swindon

Salary:

13.43 GBP / Hour

Office Angels

Expiration Date

Until further notice

Requirements

Strong attention to detail and organisational skills
Ability to work efficiently under pressure
A proactive approach to problem-solving
Team player with excellent communication skills

Job Responsibility

Administration and preparation of medical records and documentation
Efficiently scan documents using Opex scanners, achieving 800+ pages per hour
Escalate errors and queries as needed to maintain quality
Address system and hardware errors promptly
Meet operational performance targets consistently
Perform manual handling of boxes, up to 15Kg

What we offer

Be part of a dynamic team focused on operational excellence
Gain valuable experience in a critical sector
Work in a supportive environment that values your contributions

Fulltime

Document Scanner

Beacon Hill

Location:
United States , Reno

Category:
Office Administration

Contract Type:
Not provided

Salary:

Job Description:

Job Responsibility:

Requirements:

Additional Information:

Job Posted:
March 04, 2026

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