Manager, Medical Writing
- Canada, Multiple US Locations
- Medical Writing
- ICON Strategic Solutions (FSP)
- Remote
Talent Sourcing Recruiter
- Icon Strategic Solutions
About the role
This vacancy has now expired. Please click here to view live vacancies.
Manager, Medical Writing
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
As a Manager, Medical Writing at ICON, you will lead a team of medical writers to produce high-quality, scientifically accurate documents in support of clinical trials.
What You Will Do:
Your focus will be on coordinating medical writing delivery, resolving issues, and developing team capability.
Key responsibilities include:
- Managing the medical writing team, providing guidance and oversight to ensure high-quality, consistent, and scientifically sound documentation.
- Overseeing the preparation of clinical study reports, regulatory submissions, protocols, investigator brochures, and other key clinical documents.
- Collaborating closely with cross-functional teams including clinical, regulatory, and project management teams to ensure alignment and accuracy in documentation.
- Ensuring that all documents comply with applicable regulatory guidelines and internal standards while maintaining clear and concise scientific communication.
- Tracking project timelines and deliverables, ensuring that all documentation is completed and submitted within established deadlines.
- Continuously improving writing processes and templates, incorporating best practices to enhance the efficiency and quality of the medical writing function.
Your Profile:
You will have solid medical writing experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
- Bachelor's degree in life sciences, health sciences, or a related field is preferred, with extensive experience in medical writing within the pharmaceutical or clinical research industry.
- Proven experience in managing medical writing teams and overseeing the development of regulatory and clinical documents.
- Strong knowledge of regulatory requirements, clinical trial processes, and scientific writing best practices.
- Excellent writing, editing, and communication skills, with the ability to convey complex scientific concepts clearly and accurately.
- Strong organizational and leadership abilities, with experience in managing multiple projects and ensuring on-time delivery.
- Detail-oriented, adaptable, and proactive, with a commitment to maintaining the highest standards in medical writing.
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 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.
Visit our careers site to read more about the benefits ICON offers.
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.
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 or submit a request here
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.
Are you a current ICON Employee? Please click here to apply
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
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 tha
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
Teaser label
Our PeopleContent type
BlogsPublish date
02/28/2023
Summary
John Bailey, one of ICON's Veteran Leadership Transition Program Alumni shares his path from serving in the armed forces to joining the clinical research industry. ICON's Veteran Leadership T
by
John Bailey
Similar jobs at ICON
Salary
Location
US, Blue Bell (ICON)
Location
Frankfurt
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Medical Writing
Job Type
Permanent
Description
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical informa
Reference
JR152737
Expiry date
01/01/0001
Author
Kaitlyn LurkerAuthor
Kaitlyn LurkerSalary
Location
India, Bangalore
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Bangalore
Bengaluru
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical Writing
Job Type
Permanent
Description
As a Medical Writer I at ICON, you will the development and preparation of clinical trial documents, regulatory submissions, and scientific publications, contributing to the advancement of innovative
Reference
JR153060
Expiry date
01/01/0001
Author
Puja JaiswalAuthor
Puja JaiswalSalary
Location
Spain, Barcelona
Location
Barcelona
Madrid
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Medical Writing
Job Type
Permanent
Description
We are currently seeking a Senior or Principal Medical Writer to join our diverse and dynamic team. As a Senior Medical Writer at ICON, you will play a pivotal role in leading the development and exec
Reference
JR145308
Expiry date
01/01/0001
Author
Natalia RothAuthor
Natalia RothSalary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Medical Writing
Job Type
Permanent
Description
The Informed Consent Writer (ICW) is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help a candidate make an in
Reference
JR152535
Expiry date
01/01/0001
Author
Kaitlyn LurkerAuthor
Kaitlyn LurkerSalary
Location
Regional Great Britain (Northern Ireland)
Location
Dublin
Belfast
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Medical Writing
Job Type
Permanent
Description
As a Clinical Training Development Lead at ICON, you will be responsible for leading the development of innovative training programs and educational materials that enhance the learning experience for
Reference
JR151108
Expiry date
01/01/0001
Author
Rajvir SamraAuthor
Rajvir SamraSalary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Business Area
ICON Strategic Solutions (FSP)
Job Categories
Medical Writing
Job Type
Permanent
Description
The Informed Consent Writer (ICW) is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help a candidate make an in
Reference
JR149263
Expiry date
01/01/0001
Author
Kaitlyn LurkerAuthor
Kaitlyn Lurker