New · posted Oct 31
Artivion · Medical Devices
Senior Medical Writer
- Kennesaw, GA
- On-site
- Full-time
- Senior & Principal
What you need
- 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 you'll do
- 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.
Where you'll work
Kennesaw, GAOn-siteOpen in Maps (opens in a new tab)
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From the posting
About Artivion
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.
Job intelligence
The context around this role
Live data · October 31, 2026
Salary intelligence
How the pay compares
Senior & Principal roles in the US6 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| All US (middle half) | $162,375 | $186,000 | $205,875 |
Comparisons: the base pay employers published on open Clinical Evaluation & Medical Writing roles at the same level on Regulatory Jobs, October 31, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Evaluation & Medical Writing
The general path across 21 open Clinical Evaluation & Medical Writing roles on Regulatory Jobs, with the titles they carry most. Not Artivion's own promotion track.
Skills DNA
What this role leans on
How many of the posting's 28 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Documentation and SOPs9
- Clinical trial conduct5
- Collaboration and leadership5
- Investigations and CAPA4
- Regulatory submissions3
- GMP and compliance2
- Data and digital systems1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
Company hiring pulse
Artivion on Regulatory Jobs
- 9
- Open roles
- 9
- Distinct roles
- 2
- Locations
By discipline
- Clinical4 44%
- Regulatory3 33%
- Quality2 22%
By level
- Senior & Principal4 44%
- Manager2 22%
- Associate & Specialist2 22%
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Senior Medical Writer at Artivion
Open until filled.