ZipRecruiter

Log In

1

Senior Medical Writer Jobs in Decatur, GA (NOW HIRING)

Artivion

Senior Medical Writer

Kennesaw, GA · On-site

Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

Communicate with physicians, vendors, and other medical experts. * Report on adverse events, complaints, and failures associated with the product line identified through the writing process

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical ...

Enlace Health

Senior Medical Economics Analyst

Atlanta, GA · On-site

$84K - $112K/yr

Senior Medical Economics Analyst Enlace Health is a specialty value-based care company focused on ... Write advanced SQL queries to construct episode-level, provider-level, and member-month datasets ...

Enlace Health

Senior Medical Economics Analyst

Atlanta, GA · On-site

$84K - $112K/yr

Senior Medical Economics Analyst Enlace Health is a specialty value-based care company focused on ... Write advanced SQL queries to construct episode-level, provider-level, and member-month datasets ...

UCB

Senior Grants Lead (US)

Smyrna, GA · On-site

$148K - $194K/yr

As the Senior Medical Grants Lead , you will serve as UCB's global subject matter expert for medical grants and external funding, leading grant review and approval processes while driving operational ...

MiniMed

Senior Technical Writer

Atlanta, GA

$83K - $141K/yr

About the Role The Senior Technical Writer scopes, revises and drafts a variety of patient-facing technical literature needed to support a broad medical device portfolio Senior Technical Writer will ...

UCB

Senior Grants Lead (US)

Smyrna, GA

$148K - $194K/yr

As the Senior Medical Grants Lead , you will serve as UCB's global subject matter expert for medical grants and external funding, leading grant review and approval processes while driving operational ...

TIER4 GROUP

Senior Content Writer

Atlanta, GA · Remote

... Hire The Senior Content Writer will work collaboratively as a part of the creative team to ... Copyedit advice and learning content developed by medical and legal faculty. * Develop and assist ...

next page

Showing results 1-20

All JobsMedical Writer JobsSenior Medical Writer JobsSenior Medical Writer Jobs in Decatur, GA

Senior Medical Writer information

See Decatur, GA salary details

$34.2K

$134K

$241.6K

How much do senior medical writer jobs pay per year?

As of Aug 20, 2026, the average yearly pay for senior medical writer in Decatur, GA is $134,037.00, according to ZipRecruiter salary data. Most workers in this role earn between $101,500.00 and $162,100.00 per year, depending on experience, location, and employer.

What is a senior medical writer?

A Senior Medical Writer is responsible for creating clear, accurate, and compliant medical documents, including regulatory submissions, clinical study reports, and scientific publications. They work closely with cross-functional teams, such as medical affairs, regulatory affairs, and clinical teams, to ensure high-quality content. Senior Medical Writers also review and edit documents for consistency, clarity, and adherence to industry guidelines. Often, they mentor junior writers and contribute to process improvements within the medical writing team.

What are the key skills and qualifications needed to thrive as a senior medical writer?

To thrive as a Senior Medical Writer, you need advanced writing and editing skills, a thorough understanding of scientific and medical concepts, and typically a degree in a life science or related field. Familiarity with referencing tools (like EndNote), document management systems, and compliance with regulatory guidelines (such as ICH or FDA standards) is often required. Strong attention to detail, project management abilities, and the capacity to communicate complex ideas clearly are important soft skills for this position. These competencies ensure accurate, high-quality medical content that meets industry standards and supports effective communication among healthcare professionals and stakeholders.

What are some common challenges faced by senior medical writers, and how can they be addressed?

Senior Medical Writers often encounter challenges such as managing tight deadlines, interpreting complex scientific data, and ensuring adherence to strict regulatory requirements. To navigate these challenges, it's essential to have strong organizational skills, effective communication with project teams, and a solid grasp of industry guidelines. Many Senior Medical Writers find that staying current with new regulations, participating in ongoing professional development, and leveraging collaborative tools help streamline the workflow. By proactively addressing these challenges, writers can maintain accuracy and efficiency while contributing valuable expertise to cross-functional teams.

What are the most commonly searched types of Medical Writer jobs in Decatur, GA?

The most popular types of Medical Writer jobs in Decatur, GA are:

What are popular job titles related to Senior Medical Writer jobs in Decatur, GA?

For Senior Medical Writer jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Senior Medical Writer jobs in Decatur, GA look for?

The top searched job categories for Senior Medical Writer jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Senior Medical Writer jobs?

Cities near Decatur, GA with the most Senior Medical Writer job openings:

Senior Medical Writer jobs near you
Infographic showing various Senior Medical Writer job openings in Decatur, GA as of August 2026, with employment types broken down into 87% Full Time, 9% Part Time, and 4% Contract. Highlights an 60% In-person, and 40% Remote job distribution, with an average salary of $134,037 per year, or $64.4 per hour.

Senior Medical Writer

Artivion

Kennesaw, GA • On-site

Full-time

Re-posted 19 days ago

Artivion rating

8.7

Company rating: 8.7 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

Job description

Company Overview

Headquartered in suburban Atlanta, Georgia, Artivion, Inc. is a medical device company focused on developing simple, elegant solutions that address cardiac and vascular surgeons’ most difficult challenges in treating patients with aortic diseases. Artivion’s four major groups of products include: aortic stent grafts, surgical sealants, On-X mechanical heart valves, and implantable cardiac and vascular human tissues. Artivion has over 1,600 employees worldwide with sales representation in over 100 countries. The Company has manufacturing facilities located in Atlanta, Georgia, Austin, Texas and Hechingen, Germany. Additionally, it has sales and distribution offices in various countries throughout Europe, Asia, and South America. For additional information about Artivion, visit our website, www.artivion.com.

Responsibilities: 

  • Support product line compliance to US and International regulations and standards as applicable
  • Writing clinical regulatory documents including annual reports, study summaries, and other study rationales.
  • Support clinical requirements for regulatory submissions and maintenance.
  • Coordinating company deliverables such as but not limited to the CEP, CER, PMCF activities and SSCP process for MDR compliance
  • Collaborate with other departments to work as a team to accomplish tasks
  • Effectively communicate timelines and hold team members accountable to agreed upon timelines required for project dates.
  • Conduct literature reviews and write research summaries related to product line.
  • Support preparation of product IFUs and assist with labeling and labeling changes (including receipt of applicable translations).
  • Effectively present and share clinical data.
  • Develop and maintain any applicable clinical research databases as necessary.
  • Generate interim analysis, investigator meeting slides, and final clinical study reports.
  • Communicate with physicians, vendors, and other medical experts.
  • Report on adverse events, complaints, and failures associated with the product line identified through the writing process
  • Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing literature.
  • Oversee project timelines, budgets, budget change forms, accruals, and monthly reports associated with vendor supported projects
  • Generate clinical study documents including but not limited to: protocols, investigational plans, informed consent forms, handouts, SOPs, and status reports.
  • Liaison between Artivion, investigational sites, and CROs (as applicable) to coordinate and document final reports and publications.
  • Other assigned responsibilities (including previously identified tasks being performed at a higher level than one’s current title).
  • Support the development of clinical regulatory documents to support product maintenance.

Qualifications:

  • Minimum 3-4 years’ experience writing within the medical/biomedical industry.
  • BS or MS degree in biological science, epidemiology, engineering, statistics, or other science related field.
  • Knowledge of regulatory requirements relative to medical devices including Clinical Evaluation Reports and Post Market Requirements
  • Ability to write and edit quality medical abstracts, white papers, manuscripts, and other educational materials.
  • Experience with literature searches and analysis.
  • Demonstrate computer skills (spreadsheet, relational databases).
  • Excellent written and oral communication skills.
  • Excellent interpersonal skills.
  • Ability to manage multiple projects.

What Artivion employees say

Pay

Hours and flexibility

Workplace

Get the full story on Breakroom

Apply