JUMP TO CONTENT

Global Labeling Strategist

  1. United States
2025-118079
  1. ICON Strategic Solutions
  2. Regulatory Affairs

About the role

This vacancy has now expired. Please click here to view live vacancies.

Within regulatory affairs and in cross-functional teams, lead the labeling development of one asset, supervise Target Product Label initiative across the portfolio and, when needed, contribute to the labeling strategy of other assets.


  • Lead labeling development strategy in cross functional teams based on target product profile, competitor review, regulations, development data and present it to the development governance for endorsement
  • Create and maintain target product profile for one asset from phase 2 until registrational phase and for new indication of registered asset(s)
  • Create and maintain Core Company Data Sheet and, in partnership with Labeling Operation Manager, global labeling implementation plan
  • Support US affiliate in USPI creation and maintenance
  • Coordinate global labeling impact assessment of HA or internal queries of local label update in post- marketing, involving:
  • Labeling working group (LWG) - Cross functional team which members are identified in function of topics among Development team, Project team, Pharmacovigilance,
  • Regulatory leads, Medical affairs, Commercial, Legal representatives, Intellectual property, CMC, supply chain.
  • Global labeling committee (GLC) to endorse LWG proposal
  • Create and maintain processes related to labeling development activity

  • Prior experience in biologic products, medical devices, combined products
  • Prior experience in clinical development and/or regulatory affairs environment
  • Strong understanding of labeling end-to-end process and interfaces between clinical development, medical affairs, Pharmacovigilance, Regulatory, Quality and Supply Chain to ensure compliance
  • Knowledge of US, EU, Japanese labeling templates and labeling sections of eCTD dossier
  • Knowledge of health authority websites (in particular FDA, EMA websites) to retrieve label precedents and labeling regulations
  • Knowledge of electronic tools such as Dr evidence/Doc label, Adobe Acrobat Pro, Regulatory information management systems, Electronic Document Management System (e.g. Veeva Vault), other tools for labeling quality control (Text Verification Tool).
  • Detail oriented and well organized
  • Good oral and written English language skills
  • Active listening, understanding constraints from other discipline
  • Critical thinking: using logic and reasoning to identify the strength and weaknesses of alternative solutions, conclusions or approached to problems
  • Active learning: understanding the implications of new information for both current and future problem-solving and decision-making
  • Analytical skills: decision taking based on facts and figures rather than on assumptions  Team player who seeks to help and learn from colleagues
  • Bachelor’s Degree Required
  • At least 5 years of experience in global labeling strategy (development and post-marketing)

 

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others



Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, inclusion & belonging are fundamental to our culture and values.   We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.


https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

List #1

Day in the life

A picture of chemists on a superimposed periodic table
5 reasons why you should consider a career in Clinical Research

Teaser label

Inside ICON

Content type

Blogs

Publish date

01/17/2025

Summary

Five Reasons Why You Should Work at a Contract Research Organization Contract research organisations (CROs) play a pivotal role in advancing medical science, offering career opportunities tha

Teaser label

If you’re seeking a rewarding and fulfilling work environment, a career at a CRO might be the perfect fit.

Read more
Man with headphones on looking at a laptop
Tips to make a lasting impression in a video interview

Teaser label

Career Progression

Content type

Blogs

Publish date

05/10/2024

Summary

Although many employers are returning to the office, we’re still seeing a mix of both video and in-person interviews in application processes. Early in 2020, the number of companies using video

Teaser label

Ace your virtual job interview with these proven video interview tips.

Read more
Vaccination vial
The Role of Regulatory Affairs in Clinical Research

Teaser label

Industry

Content type

Blogs

Publish date

01/18/2024

Summary

Introduction to Regulatory Affairs in Clinical Research Regulatory affairs play a pivotal role in ensuring the safety, efficacy, and quality of pharmaceutical products and medical devices. I

Teaser label

Explore the pivotal role of regulatory affairs in clinical research with our insightful blog.

Read more
View all

Similar jobs at ICON

TMF Lead

Salary

Location

India, Chennai

Department

Clinical Trial Management

Location

Chennai

Remote Working

Office Based

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I

Reference

JR131639

Expiry date

01/01/0001

Kavitha K

Author

Kavitha K
Kavitha K

Author

Kavitha K
Read more Shortlist Save this role
Manager, Regulatory Strategy

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug / Device Regulatory Affairs

Job Type

Permanent

Description

We are currently seeking a Senior Regulatory Affairs Specialist to join our diverse and dynamic team. As a Senior Regulatory Affairs Specialist at ICON, you will play a pivotal role in ensuring regula

Reference

JR136787

Expiry date

01/01/0001

Melissa Benner Read more Shortlist Save this role
Senior TMF Specialist

Salary

Location

India, Chennai

Department

Clinical Trial Management

Location

Bangalore

Chennai

Bengaluru

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

Location: Chennai (Hybrid)What are we looking for:Should have 4-5 years Data Analytics IT experience.Should be specialized in Data Cleaning, Transformation, ModellingShould have experience in dashboar

Reference

JR135817

Expiry date

01/01/0001

Moushami Roy

Author

Moushami Roy
Read more Shortlist Save this role
Regulatory Affairs Manager

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Drug / Device Regulatory Affairs

Job Type

Permanent

Description

We are currently seeking a Manager, Regulatory Affairs to join our diverse and dynamic team. As a Manager, Regulatory Affairs at ICON, you will play a pivotal role in contributing to drug development

Reference

JR137141

Expiry date

01/01/0001

Bruna Duarte

Author

Bruna Duarte
Read more Shortlist Save this role
Director, Medical & Scientific Affairs (Imaging)

Salary

Location

US, Blue Bell (ICON)

Department

Full Service - Development & Commercialisation Solutions

Location

Blue Bell

Rochester

Remote Working

Office or Home

Business Area

ICON Full Service & Corporate Support

Job Categories

Drug / Device Regulatory Affairs

Job Type

Permanent

Description

We are currently seeking a Director, Medical & Scientific Affairs to join our diverse and dynamic Medical Imaging team. As a Director, Medical & Scientific Affairs at ICON, Oversees all aspects of ima

Reference

JR135501

Expiry date

01/01/0001

Muna Nelke

Author

Muna Nelke
Muna Nelke

Author

Muna Nelke
Read more Shortlist Save this role
TMF Lead

Salary

Location

UK, Reading

Location

Reading

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Regulatory Document Management

Job Type

Permanent

Description

Job DescriptionResponsibilitiesLead the setup of the TMF Study processes and Document List (SSDL)Monitor completeness and quality of TMF content for all assigned clinical trials until study close out.

Reference

JR135775

Expiry date

01/01/0001

Rajvir Samra

Author

Rajvir Samra
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above