Procedure Writer Associate Job at Wells Fargo (Bengaluru)

Bilingual Provider Relations Representative

Express Scripts Canada is seeking to hire a Bilingual Provider Relations Represe...

Location

Canada , Mississauga; Montreal

Salary:

46000.00 - 52000.00 USD / Year

The Cigna Group

Expiration Date

Until further notice

Requirements

Post-secondary school diploma or equivalent required
Basic proficiency in computer use and data entry, including familiarity with keyboarding and standard office software
Minimum of 2-3 years of experience working in an office and/or customer service environment
Proficiency in Microsoft Office applications (Word, Excel, Outlook) and Adobe Reader and Writer
Excellent written and verbal communication skills
Strong customer service focus
Ability to accurately enter, update, and maintain data in electronic systems or databases
Strong interpersonal skills, with the ability to work independently with minimal supervision as well as collaboratively in a team environment
Flexibility in adapting to new situations and change
Ability to follow clear instructions, standard procedures, and established workflows

Job Responsibility

Support for Provider Relations administrative tasks
Review and validate completed provider agreements, returning them to providers for corrections or additional information when required
Perform quality assurance checks on both self-completed work and team submissions to ensure all output meets departmental quality standards
Ensure all required agreement information for pharmacy, medical supplies and equipment, mental health care, vision care, and dental providers is accurately entered into the Express Scripts Canada system in a timely manner
Process and update provider modifications and terminations across all benefit areas accurately and within established timelines
Respond to inquiries from providers, associations, and software vendors in a professional, supportive, and customer-focused manner, in their preferred language
Collaborate with team members and support additional team deliverables as needed
Contribute to upcoming project work and perform other duties as assigned

What we offer

Competitive compensation, benefits and pension plan
Career development and advancement opportunities
A culture that celebrates innovation and collaboration
Flexible work options and wellness programs

Fulltime

Associate SEO Lead

At Rocket Clicks, we help Family Law Firms grow through focused, performance-dri...

Location

Philippines

Salary:

115000.00 - 140000.00 PHP / Month

RemotivateJobs

Expiration Date

Until further notice

Requirements

4 to 7 years of professional SEO experience, preferably in an agency environment
Proven track record of technical SEO execution
Strong hands-on experience with technical SEO audits
Experience directing or reviewing SEO content production
Demonstrated experience using and building AI workflows
Comfort reading HTML and identifying issues
Advanced Technical SEO Expertise
HTML & Site Structure Fluency
Crawl & Log Analysis proficiency
Local SEO Technical Knowledge

Job Responsibility

Conduct advanced technical audits across crawlability, indexation, rendering, site architecture, internal linking, schema, page speed, redirects, canonicalization, hreflang, and core site health
Review and refine HTML semantics across client sites
Diagnose ranking declines, indexation drops, traffic anomalies, render issues, and crawl inefficiencies
Lead crawl analysis using Screaming Frog, log file review, rendered DOM inspection, and equivalent tools
Own local SEO technical execution
Translate technical findings into clear, actionable recommendations
Review the implementation of SEO recommendations end-to-end
Stay current on algorithm updates, AI search surfaces, rendering behavior changes, structured data evolution, and emerging technical SEO standards
Direct content production by writing briefs and outlines
Structure on-page content using proper semantic HTML

What we offer

10 Paid Vacation Days per year
5 Paid Sick Days per year
10 Paid Company Holidays per year
Parental and bereavement leave
Performance bonus plan

Fulltime

Technical Writer / Business Analyst

Location

New Zealand , Auckland

Salary:

Not provided

Randstad

Expiration Date

June 12, 2026

Requirements

Expert Technical Writing: 5+ years of experience in technical writing with a 'user-centred' approach and a very high standard of written communication
BA Capability: Proven experience in functional Business Analysis, specifically in stakeholder facilitation and documentation analysis
Domain Knowledge: A strong understanding of Asset Management, Logistics, or Maintenance processes
Leadership & Drive: The ability to lead the delivery of outcomes and drive complex tasks to completion autonomously
Compliance Mindset: Experience working within large-scale, structured, or military-style organizations is highly advantageous
Must be a New Zealand citizen or permanent resident
Must be able to obtain and maintain a Confidential Security Clearance (involving a Police check)
A valid driver’s license is required for occasional regional travel

Job Responsibility

Technical Authoring: Develop and deliver a refreshed suite of user and administration guides, maritime-specific instructions, and standard operating procedure (SOP) manuals
Policy Refinement: Identify, update, and amend associated policies impacted by the system upgrade
Functional Analysis: Engage with workstream leads across Data, Maintenance, and Supply to perform subject matter knowledge transfer and identify content gaps
Stakeholder Socialisation: Facilitate engagement across all levels of the organization to socialise content and ensure 'mutually acceptable' outcomes
Process Mapping: Analyse existing artefacts and process changes to ensure the new publication hierarchy is seamless and intuitive

Fulltime

!

Cdi Query Writer

The CDI Query Writer is responsible for facilitating and distributing compliant ...

Location

United States

Salary:

Not provided

Accuity Healthcare

Expiration Date

Until further notice

Requirements

Foreign Medical Graduate
Associate's degree in nursing
Bachelor’s degree in nursing
Bachelor’s degree in health information management
Other related degree will be reviewed as the discretion of management
Minimum 3 years of clinical work experience
Minimum 2 years of current Inpatient CDI experience
MD, DO, CDIP, RN, BSN, CCS, or CCDS
Excellent communication skills
Very strong writing skills, appropriate punctuation, grammar etc.

Job Responsibility

Assess the clinical indicators and suggestions of various query requests received from the MD Reviewer/ DRG Integrity Specialist
Collaborate and communicate as necessary to clarify and avoid misinterpretation to ensure the query is optimally written and distributed to the correct client provider
Creates queries in a compliant manner in accordance with AHIMA and ACDIS compliant query guidelines as well as American Hospital Association (AHA) Coding Clinic Guidelines, ensuring that proper medical diagnoses and procedures are being submitted for reimbursement
Constructs queries with attention to detail, utilizing proper grammar and punctuation
Utilizes ICD-10 coding guidelines and medical terminology to expertly create a query which results in improved accuracy of patient severity of illness, and/or risk of mortality representing the patient’s true clinical picture in final code assignment
Participates in all educational opportunities provided by Accuity for updates in current coding and query writing guidelines as well as internal and client policies and procedures
Utilizes Accuity policies and procedures, as well as Federal and State coding reimbursement guidelines, and application of correct coding guidelines to ensure the documentation supports code assignment is at the greatest level of specificity
Will competently use Accuity tracking tool for data entry for reportable criteria
Maintains expected productivity and quality standards
Performs miscellaneous job-related duties as assigned

Principal Physician, Patient Safety

Location

India

Salary:

Not provided

Parexel

Expiration Date

Until further notice

Requirements

Experience in clinical medicine (general or specialist qualifications) which is expected to be kept up to date
Expertise in drug safety and the drug development process
Demonstrated success in technical proficiency and scientific creativity
Ability to work on complex problems requiring in-depth evaluation
Ability to exercise judgment within broadly defined practices and policies
Good presentation and verbal/written communication skills
Good interpersonal skills
Client focused approach to work
Demonstrated ability to balance technical expert responsibilities with people management duties when assigned
Computer proficiency, ability to work with web-based applications and familiarity with the Windows operating system and Microsoft Office apps

Job Responsibility

Maintaining a good working knowledge of the Adverse event/Safety profile of assigned products, labeling documents, data handling conventions, client’s guidelines and procedures, and global drug safety regulations and guidelines
Maintaining an awareness of global regulatory requirements, reporting obligations and organizing workload to ensure compliance with internal and regulatory timelines for adverse event reporting
Communicating and discussing issues related to review process with Line Manager/Project Leader/Designee
Interacting with internal and external stakeholders for resolving issues
Attending and/or presenting at client/cross functional meetings along with other stakeholders
Working as Subject Matter Experts (SMEs)
Assisting the Project Lead/Functional Lead for audits and inspections, Act as a Subject Matter Expert during Audits/inspections
Provides inputs for process improvements
Works closely with Project Lead/Functional Lead for process co-ordination and to ensure meeting all Key Performance Indicators (KPIs) for the process
Function as pharmacovigilance representative/safety scientist

Fulltime

Writer & Editor

ABEM is searching for an experienced Writer & Editor to join our Marketing and C...

Location

United States , East Lansing

Salary:

79000.00 USD / Year

ABMS

Expiration Date

Until further notice

Requirements

Bachelor’s degree in marketing, digital media, communications, journalism, or related field required
Three to five years of related experience in copywriting, editing, writing, and content development
Knowledge and experience working with associations, non-profits, and/or board governance
Health care or higher education industry experience preferred
Proper English usage, grammar, spelling, punctuation, and vocabulary with superior writing, proofreading, and editing skills
Proven ability to communicate in written form utilizing journalistic, technical, and consumer-marketing writing styles based on audience
Experience and proven skills in writing, copywriting, editing, and proofing using Associated Press (AP) style
Experience working with content management systems and web platforms
Knowledge of communications media, publications, and marketing best practices
utilization of social media marketing and other web-based communication mediums

Job Responsibility

Serves as the primary writer and editor for content for ABEM publications
Ensures the uniformity of ABEM's style across all print and digital materials utilized both internally and externally
Responsible for crafting communications on behalf of the organization and the Board of Directors, which includes content strategy, messaging, and the production of publications, media releases, and web-based materials
Develops copy in various styles, including formal, technical, and marketing, customized to align with the target audience and intended objectives
Collaborates closely with executive leadership to stay current on initiatives and programs at ABEM to develop effective messaging and talking points that support the organization
Oversees complex review and publication schedules, maintenance strategies, and the systematic organization of content, documents, and media lists
Writes and manages technical and editorial materials for ABEM publications, external publications, and the ABEM website
Executes communications plans for ABEM publications and organization-wide projects, including content development, review and editing timelines, sequencing, and monitoring of deadlines
Edits materials for content and ABEM style
Maintains ABEM Style Guide

Fulltime

Global Regulatory Writing Manager

To author and gain approval of scientific and regulatory submission documents th...

Location

Japan , Tokyo

Salary:

Not provided

Amgen

Expiration Date

Until further notice

Requirements

Doctorate degree
OR Master’s degree and 3 years of directly related experience
OR Bachelor’s degree and 5 years of directly related experience
OR Associate’s degree and 10 years of directly related experience
OR High school diploma / GED and 12 years of directly related experience
Ability to analyze scientific data and interpret its significance in practical applications, with limited oversight
Excellent written/oral communication skills and attention to detail in local native language
Upper-intermediate level business English (capable of communicating appropriately in most situations, equivalent to TOEIC score of 730+
Highly skilled word processing and other Microsoft Office Programs
Significant knowledge of scientific/technical writing and editing, and of overall clinical development process for new compounds

Job Responsibility

Author regulatory submission documents, as assigned, including Table of All Studies, Clinical Overview Addenda, eCTD Module 2 Clinical Summary Documents, Briefing Documents, and other regulatory documents according to the local needs
Conduct the formal review and approval of authored documents, following applicable standard operating procedures
With considerable supervision, manage regulatory writing activities for local product submissions, including new and supplemental drug applications/biologics license applications
Serve as functional area lead on local product teams - May provide functional area input for Local Regulatory Plan and team goals
Work with CRO and freelance writers
Participate in departmental and cross-departmental initiatives as appropriate
May participate in training and mentoring of junior regulatory writers
May participate in departmental and cross-departmental initiatives, as appropriate
Generate document timelines, with team input
Keep abreast of relevant professional information and technology

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

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Procedure Writer Associate

Job Description

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