ZipRecruiter

Log In

1

Senior Medical Writer Oncology Jobs in Decatur, GA

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 ...

YO AI Labs

Medical Writer - Remote

Atlanta, GA · Remote

$50 - $90/hr

Medical Writer Expert Remote Location: Remote Job Type: Contractor Pay: $50-$80/hour Job Overview ... Experience in oncology and haematology is preferred.

micro1 AI

Medical Writing Manager

South Fulton, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

micro1 AI

Medical Writing Manager

Atlanta, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

micro1 AI

Medical Writing Manager

Sandy Springs, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

micro1 AI

Medical Billing Specialist

South Fulton, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

micro1 AI

Medical Billing Specialist

Sandy Springs, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

micro1 AI

Medical Billing Specialist

Atlanta, GA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Role Type: Contractor Location: Remote micro1 is engaging ... Experience across multiple clinical phases and therapeutic areas; oncology and haematology ...

Enlace Health

Senior Medical Economics Analyst

Atlanta, GA · On-site

$84K - $112K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

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 ...

Amgen SA

Senior Medical Science Liaison - Obesity - GA

Atlanta, GA · On-site

$140 - $190/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

With our focus on four therapeutic areas -Oncology, Inflammation, General Medicine, and Rare ... Senior Medical Science Liaison - Obesity - GA The Territory will include Northern Georgia What you ...

Taiho Oncology, Inc.

Sr. Manager, Medical Field

Atlanta, GA · On-site

$178.50 - $210/hr

  • Retirement

  • PTO

Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and ... Excellent English communication skills, both verbal and written. * Individual should be able to ...

next page

Showing results 1-20

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

Senior Medical Writer Oncology information

See Decatur, GA salary details

$34.2K

$134K

$241.6K

How much do senior medical writer oncology jobs pay per year?

As of Aug 20, 2026, the average yearly pay for senior medical writer oncology 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 does a senior medical writer in oncology do?

A Senior Medical Writer in Oncology is responsible for creating, editing, and reviewing scientific documents related to cancer research, clinical trials, and treatments. They work closely with researchers, clinicians, and regulatory teams to ensure the accuracy and clarity of materials such as clinical study reports, manuscripts, and regulatory submissions. Their role is critical in communicating complex oncology data to both scientific and non-scientific audiences, while also ensuring compliance with industry regulations and guidelines.

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

To thrive as a Senior Medical Writer in Oncology, you need a strong background in life sciences or medicine, advanced scientific writing skills, and experience with oncology research or clinical trials. Familiarity with regulatory submission standards, literature databases, and software like EndNote or Adobe InDesign is typically expected. Exceptional attention to detail, project management abilities, and effective collaboration and communication skills help set you apart in this role. These skills ensure the production of accurate, compliant, and high-impact scientific documents that support drug development and regulatory approval processes.

How does a senior medical writer in oncology typically collaborate with cross-functional teams during the preparation of regulatory and scientific documents?

As a Senior Medical Writer in Oncology, you will work closely with clinical research, regulatory affairs, biostatistics, and medical affairs teams to ensure the accuracy and clarity of documents such as clinical study protocols, regulatory submissions, and manuscripts. This role often involves participating in project meetings, gathering input from subject matter experts, and integrating feedback to produce high-quality deliverables within tight timelines. Effective communication and the ability to translate complex scientific data into clear, compliant documents are key to successful collaboration in this multidisciplinary environment.

What is the difference between Senior Medical Writer Oncology vs Medical Writer Oncology?

AspectSenior Medical Writer OncologyMedical Writer Oncology
Required CredentialsAdvanced degree (MD, PhD), experience in oncologyBachelor's or Master's degree, entry-level experience
Work EnvironmentLeading projects, mentoring junior writers, client interactionsSupporting document creation, research, and drafting
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsMedical communications agencies, pharma companies
Search & Comparison IntentUnderstanding senior roles, career progressionEntry-level responsibilities, skill development

The main difference between Senior Medical Writer Oncology and Medical Writer Oncology lies in experience, responsibilities, and seniority. Senior Medical Writers typically lead projects, mentor junior staff, and have more advanced credentials, while Medical Writers focus on supporting document creation and research. Both roles are essential in the oncology medical writing field, but the senior position involves greater leadership and strategic input.

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

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

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

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

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

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

Senior Medical Writer Oncology jobs near you
Infographic showing various Senior Medical Writer Oncology job openings in Decatur, GA as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 16% Part Time, and 5% Contract. Highlights an 89% Physical, 1% Hybrid, and 10% 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