The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
The Associate Director is a key leadership position responsible for determining and driving the ... Senior Medical Writer(s) and Medical Writer(s) will report to this role Main Responsibilities and ...
Associate Medical Editor - Remote
Raleigh, NC · Remote
$85K - $90K/yr
The Associate Medical Editor performs literature searches, writes, reviews, and edits evidence-based cancer information tailored to multiple literacy levels and audience needs that covers the ...
Associate Medical Editor - Remote
Raleigh, NC · Remote
$85K - $90K/yr
The Associate Medical Editor performs literature searches, writes, reviews, and edits evidence-based cancer information tailored to multiple literacy levels and audience needs that covers the ...
Scientific Lead - Medical Communications ICON is a global healthcare intelligence and clinical ... This role encompasses high-level writing, peer-review of project deliverables, strategic support ...
Scientific Lead - Medical Communications ICON is a global healthcare intelligence and clinical ... This role encompasses high-level writing, peer-review of project deliverables, strategic support ...
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
Medical Director, Cardiology
Durham, NC · On-site
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
Medical Director, Cardiology
Durham, NC · On-site
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
The Associate Medical Director / Medical Director will provide medical, clinical and scientific ... both written and spoken). * Robust and current knowledge of scientific, clinical, regulatory ...
Med Info Assoc I
$18.45 - $20.50/hr
Medical Information Associate I The Medical Information Associate I provides accurate technical and ... Strong written and verbal communication skills for interacting with healthcare professionals ...
Quick apply
Med Info Assoc I
$18.45 - $20.50/hr
Medical Information Associate I The Medical Information Associate I provides accurate technical and ... Strong written and verbal communication skills for interacting with healthcare professionals ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site +1
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site +1
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
POSTDOCTORAL ASSOCIATE
Durham, NC · On-site
... associate to join their team. The postdoc's research projects will focus on inherited metabolic ... medical writing in peer-reviewed medical journals, or platform/poster presentations in conferences ...
Dodge Service Writer
Cary, NC · On-site
Reasonable accommodations may be made to enable individuals with medical conditions to perform the ... Desired Education: o GED High School Diploma o Associate Degree o Bachelor Degree o Master Degree o ...
Dodge Service Writer
Cary, NC · On-site
Reasonable accommodations may be made to enable individuals with medical conditions to perform the ... Desired Education: o GED High School Diploma o Associate Degree o Bachelor Degree o Master Degree o ...
Dodge Service Writer
Cary, NC · On-site
Reasonable accommodations may be made to enable individuals with medical conditions to perform the ... Desired Education: o GED • High School Diploma o Associate Degree o Bachelor Degree o Master ...
Dodge Service Writer
Cary, NC · On-site
Reasonable accommodations may be made to enable individuals with medical conditions to perform the ... Desired Education: o GED • High School Diploma o Associate Degree o Bachelor Degree o Master ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
The Med Tech positionis a multifaceted role that involves being a care provider, medical aide, and ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
The Med Tech positionis a multifaceted role that involves being a care provider, medical aide, and ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
The Med Tech positionis a multifaceted role that involves being a care provider, medical aide, and ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
The Med Tech positionis a multifaceted role that involves being a care provider, medical aide, and ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Med Tech
Raleigh, NC · On-site
Description The Med Tech position is a multifaceted role that involves being a care provider ... Ability to follow written and oral instructions and procedures. * Associates in this role are ...
Associate Medical Writer information
See Raleigh, NC salary details
$13.79 - $17.65
3% of jobs
$17.65 - $21.52
9% of jobs
$25.30 is the 25th percentile. Wages below this are outliers.
$21.52 - $25.38
13% of jobs
$25.38 - $29.25
7% of jobs
$29.25 - $33.12
8% of jobs
$33.12 - $36.98
5% of jobs
The median wage is $38.67 / hr.
$36.98 - $40.85
8% of jobs
$40.85 - $44.71
16% of jobs
$46.21 is the 75th percentile. Wages above this are outliers.
$44.71 - $48.58
12% of jobs
$48.58 - $52.45
7% of jobs
$52.45 - $56.31
11% of jobs
$13
$37
$56
How much do associate medical writer jobs pay per hour?
As of Jul 12, 2026, the average hourly pay for associate medical writer in Raleigh, NC is $37.56, according to ZipRecruiter salary data. Most workers in this role earn between $25.48 and $47.45 per hour, depending on experience, location, and employer.
What are the key skills and qualifications needed to thrive as an Associate Medical Writer, and why are they important?
To thrive as an Associate Medical Writer, you need a solid background in life sciences, strong writing abilities, and attention to detail, often supported by a relevant degree such as biology, pharmacy, or medicine. Familiarity with referencing tools (e.g., EndNote), medical literature databases (e.g., PubMed), and proficiency in Microsoft Office are typically required. Excellent communication, time management, and the ability to interpret complex scientific data set standout candidates apart. These skills ensure that scientific information is accurately and clearly communicated to varied audiences, supporting effective healthcare and regulatory decision-making.
What are some common challenges faced by Associate Medical Writers during their first year on the job?
In their first year, Associate Medical Writers often find it challenging to quickly adapt to diverse writing styles and strict formatting guidelines required by different clients or regulatory bodies. Balancing tight deadlines while ensuring scientific accuracy and compliance can also be demanding, especially when juggling multiple projects. Additionally, learning to effectively collaborate with multidisciplinary teams—including clinicians, researchers, and senior writers—requires strong communication and organizational skills. However, with mentorship and constructive feedback, these challenges become valuable learning opportunities for professional growth.
What is the difference between Associate Medical Writer vs Medical Writer?
| Aspect | Associate Medical Writer | Medical Writer |
|---|---|---|
| Required credentials | Bachelor's degree, often in life sciences or related field | Bachelor's or higher degree, often with some experience |
| Work environment | Entry-level, training-focused, often in pharmaceutical or biotech companies | More independent, involved in complex document creation for regulatory or scientific purposes |
| Employer usage | Pharmaceutical, biotech, medical communications agencies | Pharmaceutical companies, CROs, medical communication firms |
The main difference between an Associate Medical Writer and a Medical Writer lies in experience and responsibility. Associate Medical Writers are typically entry-level, focusing on learning and supporting document preparation, while Medical Writers handle more complex projects independently. Both roles require similar educational backgrounds and are common in the pharmaceutical and biotech industries.
What does an Associate Medical Writer do?
An Associate Medical Writer is responsible for creating scientific documents, such as clinical study reports, regulatory submissions, and manuscripts for publication. They work closely with medical professionals, researchers, and regulatory teams to ensure accuracy and compliance with guidelines. Their role often involves interpreting complex scientific data and presenting it in a clear, concise manner for different audiences. Associate Medical Writers are typically early in their medical writing careers and receive guidance from more senior writers as they develop their skills.
What are the most commonly searched types of Medical Writer jobs in Raleigh, NC? The most popular types of Medical Writer jobs in Raleigh, NC are:
What are popular job titles related to Associate Medical Writer jobs in Raleigh, NC? For Associate Medical Writer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Associate Medical Writer jobs in Raleigh, NC look for? The top searched job categories for Associate Medical Writer jobs in Raleigh, NC are:
- Medical Information
- Associate Director Medical Writing
- Freelance Health Science Writer
- Remote Medical Device Technical Writer
- Remote Technical Documentation Writer
- Freelance Pharmacist Medical Writer
- Remote Contract Medical Affairs
- Freelance Medical Writing
- Contract Medical Writing
- Internship Pharmd Medical Writer
What cities near Raleigh, NC are hiring for Associate Medical Writer jobs? Cities near Raleigh, NC with the most Associate Medical Writer job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
55th of 210 rated it services
Job description
The Associate Director is a key leadership position responsible for determining and driving the medical writing strategy for one or more therapeutic areas within Clinical Development.
As a strategic partner to senior clinical leadership, the incumbent is accountable for the efficient preparation of high quality, strategically aligned medical writing deliverables that support the clinical development, clinical safety and regulatory requirements of a clinical program. He or she is also responsible for the messaging strategy across a program of work, for the provision of strategic input into the development of clinical development plans and submission plans, and for analysing proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency
This role has global responsibilities with potential for global reports, participation in global teams and interaction with regulatory agencies in multiple regions
Main Responsibilities and Accountabilities
Drives and develops the messaging strategy within the therapeutic area to ensure effective communication underpins successful clinical development
Experience
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
As a strategic partner to senior clinical leadership, the incumbent is accountable for the efficient preparation of high quality, strategically aligned medical writing deliverables that support the clinical development, clinical safety and regulatory requirements of a clinical program. He or she is also responsible for the messaging strategy across a program of work, for the provision of strategic input into the development of clinical development plans and submission plans, and for analysing proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency
This role has global responsibilities with potential for global reports, participation in global teams and interaction with regulatory agencies in multiple regions
- This role reports to the Director of Medical Writing
- Senior Medical Writer(s) and Medical Writer(s) will report to this role
Main Responsibilities and Accountabilities
- Leads the Medical Writing contributions to assigned therapeutic area(s). Key accountabilities:
- Maintain a collaborative and strategic partnership with Global Therapeutic Area Leads, Global Clinical Program Directors and Clinial Safety Physicians to ensure understanding of Clinical Development strategy for the therapeutic area and the nature of medical writing services required to deliver on company objectives
- Critiques ability of product strategy (eg, submission plans) to deliver on business objectives or meet regulatory needs, and identify where new or alternative arguments are needed.
- Leads cross-functional teams to develop a messaging strategy across a program of work (eg, building a clinical submission)
- The efficient preparation of medical writing deliverables for assigned clinical program(s) according to budget and timelines
- Forecasting, budgeting, resource planning and resource allocation.
- Managing (Senior) Medical Writer(s) within therapeutic area(s). Coach, train and mentor staff, thereby contributing to successful clinical development, product registration in key regions and commercialization of new compounds, including important lifecycle management work
Drives and develops the messaging strategy within the therapeutic area to ensure effective communication underpins successful clinical development
- Responsible for aligning, coordinating and building consistent information and messages across all individual documents within a clinical program, starting with intial strategic plans, continuing through study level documents to final program level deliverables (ie, regulatory submission or publication of key journal articles for a publication plan).
- Interfaces with Global Therapeutic Area Heads, Global Clinical Program Directors and Clinial Safety Physicians to ensure that the communication needs for clinical data are considered early in the development program to enable consistency of data presentation and messaging throughout the clinical development process.
- Analyses proposed plans, programs, individual studies and related documents for their ability to deliver the information required by the target audience (ie, regulatory authority) in a compelling fashion with accuracy and consistency.
- Understands where all intended messages will be located across individual documents within a clinical program, and ensures alignment of messages across documents.
- Understands issues affecting the design of clinical development strategy, and understands how study design, data capture and statistical analysis plan design will affect downstream documents.
- Responsible for ensuring that statements included in the deliverables are accurate and supported by appropriate data
- Accountable for medical writing deliverable quality and ensures adherence to departmental procedures / practices, and industry / international standards.
- Responsible for the development, implementation and communication of Best Practices, SOPs, templates, work instructions, style guides and content guides to ensure efficient preparation of high quality medical writing deliverables.
- Cultivates an understanding of modern medical writing processes and solutions through survey of relevant literature, attendance at meetings and use of international external networks.
- Responsible for continual improvement of in-house medical writing.
- Provides expert medical writing support to other CR&D and CSL groups where required
- In collaboration with Director, Medical Writing and Disclosure, ensures appropriate medical writing support for the clinical programs including forecasting, budgeting, resource planning and resource allocation
- Responsible for building and maintaining collaborative relationships with medical writing partner(s) (CRO, vendor, alliance partner, etc) to ensure an effective, efficient, productive and professional working relationship. Participates in vendor governance.
- Participant in bid defense, contract development, work alignment and / or operation meetings.
- Post-graduate qualifications (PhD or MD preferred)
Experience
- A minimum of 8 years medical writing experience within the biopharmaceutical
- industry or a contract research organization.
- A minimum of 3 years in a supervisory role
- A comprehensive understanding of the clinical development process, including the
- documents that are required at each stage.
- A comprehensive understanding of medical writing processes, standards and issues.
- Demonstrated track record in cross-functional, multicultural and international clinical trial teams
- Excellent verbal, written and presentation skills.
- Mastery of the English language, with a comprehensive understanding of English grammar and punctuation
- Prior experience with submissions in Common Technical Document (CTD) format.
- Knowledge of eTechnology related to regulatory submission activities (eCTD, EDMS, Life Cycle Management
- Expert MS Office skills with a special focus on word processing, tables, spreadsheets, presentations, graphics and template
IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world. Learn more at https://jobs.iqvia.com
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/eoe
As the COVID-19 virus continues to evolve, IQVIA's ability to operate and provide certain services to customers and partners necessitates IQVIA and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/covid-19-vaccine-status
About IQVIA
Sourced by ZipRecruiter
At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.
Industry
Health care and social assistance
Company size
10,000+ Employees
Headquarters location
Durham, NC, US