Blue Bell, PA · On-site
Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Blue Bell, PA · On-site
Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Blue Bell, PA · On-site +1
Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Blue Bell, PA · On-site +1
Principal Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
Be Seen First
OR · Remote
$85 - $90/hr
Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in ...
Quick apply
Be Seen First
OR · Remote
$85 - $90/hr
Medical Writer Contract Position - 6 months with potential extension Position Summary Our client is seeking an experienced Medical Writer to develop high-quality clinical and regulatory documents in ...
San Diego, CA · On-site
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
San Diego, CA · On-site
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
Boston, MA · On-site
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...
Quick apply
Boston, MA · On-site
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...
Cambridge, MA · On-site
$134K - $162K/yr
RESPONSIBILITIES The Senior Medical Writer position requires writing and editing of clinical and scientific reports including summaries from statistical analyses for submission to regulatory agencies ...
Quick apply
Cambridge, MA · On-site
$134K - $162K/yr
RESPONSIBILITIES The Senior Medical Writer position requires writing and editing of clinical and scientific reports including summaries from statistical analyses for submission to regulatory agencies ...
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
Quick apply
Assume a Product Medical Writer responsibility, providing strategic medical writing expertise and support to multiple projects in a clinical development program. * Ensure high technical quality of ...
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Senor Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
New
Senor Medical Writer ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven ...
New
Boston, MA · On-site
$150K - $180K/yr
Description of Role The Senior Medical Writer will be responsible for authoring and managing clinical regulatory documents in support of the company's clinical development program and objectives.
New
Boston, MA · On-site
$150K - $180K/yr
Description of Role The Senior Medical Writer will be responsible for authoring and managing clinical regulatory documents in support of the company's clinical development program and objectives.
New
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the field of medical communications, is growing! We are seeking a Senior Medical Writer to join our team.
Senior Medical Writer - Publications Ashfield MedComms, an exciting and innovative leader in the field of medical communications, is growing! We are seeking a Senior Medical Writer to join our team.
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Boston, MA · Hybrid
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...
Boston, MA · Hybrid
$71K - $76K/yr
Analysts and Medical Writers work on projects involving the detailed analysis of data from clinical trials and the assimilation and creative presentation of this analysis in different formats ...
The Medical Writer is responsible for medical documentation summarizing risks and benefits in support of the development, license application and approval, and post-marketing development of one or ...
The Medical Writer is responsible for medical documentation summarizing risks and benefits in support of the development, license application and approval, and post-marketing development of one or ...
Durham, NC · On-site
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...
Durham, NC · On-site
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...
Durham, NC · On-site
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...
Durham, NC · On-site
Acts as Lead Medical Writer on most types of writing projects. Prepares assigned documents in accordance with IQVIA Standard Operating Procedures (SOPs) and customer requirements as well as to the ...
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Senior Medical Writer The Senior Medical Writer independently plans and prepares a range of regulatory documents and medical communications to support all phases of product development. The primary ...
Boston, MA · On-site
$150K - $180K/yr
Description of Role The Senior Medical Writer will be responsible for authoring and managing clinical regulatory documents in support of the company's clinical development program and objectives.
New
Boston, MA · On-site
$150K - $180K/yr
Description of Role The Senior Medical Writer will be responsible for authoring and managing clinical regulatory documents in support of the company's clinical development program and objectives.
New
Boston, MA · Hybrid
$54K - $66K/yr
This role is available in our Boston office About the Role Our Analyst/Medical Writer Internship is ideal for current students and recent graduates in scientific disciplines, eager to gain valuable ...
Boston, MA · Hybrid
$54K - $66K/yr
This role is available in our Boston office About the Role Our Analyst/Medical Writer Internship is ideal for current students and recent graduates in scientific disciplines, eager to gain valuable ...
$14.18 - $18.16
3% of jobs
$18.16 - $22.14
9% of jobs
$26.03 is the 25th percentile. Wages below this are outliers.
$22.14 - $26.11
13% of jobs
$26.11 - $30.09
7% of jobs
$30.09 - $34.07
8% of jobs
$34.07 - $38.05
5% of jobs
The median wage is $39.79 / hr.
$38.05 - $42.02
8% of jobs
$42.02 - $46
16% of jobs
$47.54 is the 75th percentile. Wages above this are outliers.
$46 - $49.98
12% of jobs
$49.98 - $53.96
7% of jobs
$53.96 - $57.93
11% of jobs
$14
$38
$57
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 2 days ago
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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 information.
What You Will Do:
You will oversee medical writing workstreams, ensuring deliverables meet quality and timeline expectations.
Key responsibilities include:
Leading the preparation and review of clinical study reports, protocols, and other regulatory documents to ensure accuracy and clarity
Collaborating with cross-functional teams, including clinical research, biostatistics, and regulatory affairs, to gather and synthesize information for document development
Providing guidance on best practices for medical writing and ensuring adherence to regulatory requirements and internal standards
Mentoring and training junior medical writers, fostering a culture of excellence and professional growth
Staying current with industry trends and regulatory guidelines to inform writing practices and maintain high-quality outputs
Acting as a lead medical writer for complex projects and leading clinical/regulatory marketing approval applications for new biologics and drugs
The position includes all duties of a Senior Medical Writer, as well as leadership of regulatory approval application writing
Your Profile:
You will have solid experience in medical writing, with the ability to manage competing priorities and develop your team.
Required qualifications and experience:
A bachelor's degree in life sciences, pharmacy, or a related discipline
Significant experience in medical writing, particularly in regulatory submissions and clinical documentation
Strong understanding of regulatory requirements and industry standards for clinical writing
Exceptional writing and editing skills, with a keen eye for detail and clarity
Excellent communication and interpersonal skills, enabling effective collaboration with diverse teams and stakeholders
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a requesthere.
Are you a current ICON Employee? Please click here to apply
