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Medical Publications Manager Jobs in Decatur, GA

CryoLife

Senior Medical Writer

Kennesaw, GA · On-site

Coordinate the execution of peer-reviewed projects (publications, posters, abstracts) and marketing ... Ability to manage multiple projects. Equal Opportunity Employer This employer is required to notify ...

3:15

Medical Assistant (in office)

Douglasville, GA · On-site

$18/hr

Ensure patients are signed up for Chronic Care Management (CCM) as well as any other program the ... publications. * Serve and protect the practice by adhering to professional standards, facility ...

3:15

Medical Assistant (in office)

Douglasville, GA · On-site

$18/hr

Ensure patients are signed up for Chronic Care Management (CCM) as well as any other program the ... publications. * Serve and protect the practice by adhering to professional standards, facility ...

3:15

Medical Assistant (in office)

Douglasville, GA · On-site

$18/hr

Ensure patients are signed up for Chronic Care Management (CCM) as well as any other program the ... publications. * Serve and protect the practice by adhering to professional standards, facility ...

MMS

Senior Medical Writer (Remote)

Atlanta, GA · On-site

... publications to medical journals * Complete writing assignments in a timely manner * Maintain ... Contribute substantially to, or manages, production of interpretive guides * Take ownership of a ...

Lukos

Medical Clinician- Pediatrician

Atlanta, GA · On-site

$166K - $215K/yr

... management of congenital anomalies, birth defects, congenital heart defects, or pediatric ... Experience contributing to scientific publications, technical reports, presentations, and clinical ...

Lukos

Medical Clinician- Pediatrician

Atlanta, GA · On-site

$163K - $211K/yr

... management of congenital anomalies, birth defects, congenital heart defects, or pediatric ... Experience contributing to scientific publications, technical reports, presentations, and clinical ...

Lukos

Medical Clinician- Pediatrician

Atlanta, GA · On-site

$166K - $215K/yr

... management of congenital anomalies, birth defects, congenital heart defects, or pediatric ... Experience contributing to scientific publications, technical reports, presentations, and clinical ...

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All JobsMedical Publications JobsMedical Publications Manager JobsMedical Publications Manager Jobs in Decatur, GA

Medical Publications Manager information

See Decatur, GA salary details

$14

$43

$72

How much do medical publications manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for medical publications manager in Decatur, GA is $43.21, according to ZipRecruiter salary data. Most workers in this role earn between $28.17 and $56.35 per hour, depending on experience, location, and employer.

What does a medical publications manager do?

A Medical Publications Manager oversees the development, review, and dissemination of scientific and medical information produced by a pharmaceutical or healthcare company. Their responsibilities include managing the creation of manuscripts, abstracts, posters, and presentations for medical conferences and journals. They collaborate with medical writers, researchers, and key opinion leaders to ensure accuracy, compliance with regulations, and alignment with strategic objectives. Additionally, they help ensure that publication plans support the communication of clinical trial results and other research findings to the medical community.

What skills and qualifications are needed to be a medical publications manager?

To thrive as a Medical Publications Manager, you need a solid background in life sciences, experience in scientific writing, and familiarity with publication guidelines such as GPP and ICMJE. Proficiency with reference management software, publication planning tools, and often a relevant certification (e.g., CMPP) is highly valued. Exceptional project management, attention to detail, and strong interpersonal skills set outstanding candidates apart. These abilities are crucial for ensuring timely, compliant, and impactful dissemination of scientific information to the medical community.

How does a medical publications manager collaborate with cross-functional teams during the publication development process?

A Medical Publications Manager plays a central role in coordinating with various cross-functional teams such as medical writers, clinical researchers, regulatory affairs, and marketing to ensure accuracy and compliance in publication content. They facilitate regular meetings to align on timelines, data interpretation, and messaging, while also managing external agencies and key opinion leaders for manuscript development and review. Effective collaboration helps streamline the approval process and ensures that all publications adhere to industry standards and company policies.

What is the difference between Medical Publications Manager vs Medical Writer?

AspectMedical Publications ManagerMedical Writer
CredentialsTypically requires a degree in life sciences, healthcare, or related field; often advanced degrees or certifications in medical writing or publication managementUsually holds a degree in life sciences, healthcare, or communications; certifications like AMWA or EMWA are common
Work EnvironmentManages publication projects, coordinates with authors, and oversees publication strategies within pharmaceutical or healthcare companiesPrepares, writes, and edits scientific documents, including manuscripts, regulatory documents, and promotional materials
Employer & Industry UsageUsed in pharmaceutical, biotech, and healthcare industries for publication planning and managementCommonly employed in medical communication agencies, pharmaceutical companies, and research institutions for content creation

The Medical Publications Manager focuses on overseeing publication strategies and managing teams, while the Medical Writer is primarily responsible for creating and editing scientific content. Both roles require relevant scientific knowledge and communication skills, but their core responsibilities differ significantly.

What are popular job titles related to Medical Publications Manager jobs in Decatur, GA?

For Medical Publications Manager jobs in Decatur, GA, the most frequently searched job titles are:

What job categories do people searching Medical Publications Manager jobs in Decatur, GA look for?

The top searched job categories for Medical Publications Manager jobs in Decatur, GA are:

What cities near Decatur, GA are hiring for Medical Publications Manager jobs?

Cities near Decatur, GA with the most Medical Publications Manager job openings:

Medical Publications Manager jobs near you
Infographic showing various Medical Publications Manager job openings in Decatur, GA as of August 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 50% In-person, and 50% Remote job distribution, with an average salary of $89,875 per year, or $43.2 per hour.

Senior Medical Writer

Artivion

Kennesaw, GA • On-site

Full-time

Re-posted 22 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.

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