Medical Information Manager (US Remote)
- United States
- Clinical Trial Support
- ICON Strategic Solutions
- Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
As a (job title) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
What you will be doing:
Looking for a Medical Affairs, Medical Reviewer candidate that will be primarily responsible for the medical accuracy review of promotional materials containing medical content for later-stage, post-launch US products.
You are:
- Represent Medical Affairs in medical review of promotional materials for assigned product(s)/therapeutic area(s), as determined by Client’s business needs. May also include medical review of non-promotional materials
- Provide timely, medically-relevant, scientifically-sound, and fair-balanced medical/scientific reviews of materials submitted for promotional and/or non-promotional review for assigned product(s)/therapeutic area(s), as determined by Client’s business needs
- Critically review and may provide solutions to complex promotional and medical pieces to ensure balance of the messages, medical accuracy, and appropriateness of the content of the materials/activities.
- Review and approve promotional materials containing information on company’s marketed products as well as the corresponding disease states developed for US markets
- Cross check scientific information in materials against cited references and ensure data included are accurate, within context and presented in a fair/scientifically-balanced manner.
- Verify substantiation of all claims and comparisons. Advise on whether claims are consistent with appropriate approved label
- Participate in meetings, as required, to liaise with client stakeholders and resolve partially accepted or rejected comments after discussing with key stakeholders (med affairs lead, regulatory, legal etc.)
- Advise on materials and events designed and produced by US marketing and medical teams to ensure compliance with company policies and standards for ethical promotion and scientific interactions.
- Based on business needs, candidates may manage other medical information deliverables.
Requirements:
- Advanced bioscience or pharmacy/medical qualification (PharmD, PhD, MD, post-doctoral, etc.).
- Overall, 4-6 years of experience in pharmaceutical industry in reviewing promotional/non-promo materials
- Knowledge of US regulatory guidelines affecting the promotional and non-promotional material review
- Strong accountability, interpersonal and organizational skills, and the ability to work in a cross-functional team environment.
- Excellent verbal and written communication skills and willingness to travel on as needed basis.
Why ICON?
Our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.
ICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know.
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.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
.jpg)
Teaser label
Inside ICONContent type
BlogsPublish 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 that are
.jpg)
Teaser label
Career ProgressionContent type
BlogsPublish 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 interv

Teaser label
Career ProgressionContent type
BlogsPublish date
07/20/2023
Summary
Unlocking your Potential: The Benefits of ICON’s EPIC Internship Program Internship programs have become a vital stepping stone for students and young professionals seeking to gain practic
Similar jobs at ICON
Salary
Location
Netherlands
Department
Clinical Operations Roles
Location
Netherlands
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Clinical Research Coordinator (SMAII) located in the area Eindhoven you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence
Reference
2025-121015
Expiry date
01/01/0001
Author
Iris BrouwerAuthor
Iris BrouwerSalary
Location
France, Paris
Department
Clinical Monitoring
Location
Paris
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As an In-House Clinical Research Associate (IHCRA), you will support our global pharmaceutical clients, with whom ICON shares a culture of innovation, flexibility, and a common vision: bringing to mar
Reference
JR132369
Expiry date
01/01/0001
Author
Sophie ClarkeAuthor
Sophie ClarkeSalary
Location
Bulgaria, Sofia
Location
Sofia
Bucharest
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Study Delivery Specialist (Global Project Associate/Analyst) to join our diverse and dynamic team.We are looking for candidates who have experience in global study managemen
Reference
JR136508
Expiry date
01/01/0001
Author
Dariusz SternlichtAuthor
Dariusz SternlichtSalary
Location
Korea, Seoul
Location
Seoul
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Site Management Associate I to join our diverse and dynamic team. As a Site Management Associate I at ICON, you will play an important role in supporting the management of c
Reference
JR133662
Expiry date
01/01/0001
Author
Daisy ParkAuthor
Daisy ParkSalary
Location
Japan, Tokyo
Department
Clinical Monitoring
Location
Osaka
Tokyo
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and managem
Reference
JR129234
Expiry date
01/01/0001
Author
Sachi TakamuneAuthor
Sachi TakamuneSalary
Location
Mexico, Mexico City
Department
Clinical Monitoring
Real World Solutions
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking an IHCRA (In-House Clinical Research Associate) to join our diverse and dynamic team. As an IHCRA at ICON, you will play a pivotal role in supporting the execution and managem
Reference
JR135435
Expiry date
01/01/0001
Author
Olivia MolinaAuthor
Olivia Molina