APremium Healthcare Solution, LLC has been serving the Conyers, GA community for over 10 years, providing exceptional healthcare services tailored to individual needs. Our commitment to quality care and innovative solutions has earned us the trust of our patients and the admiration of our dedicated employees, who thrive in a supportive and empowering work environment.

Medical Writer

Medical writerMedical writerFull TimeRemoteTeam 51-200Since 2004H1B No SponsorCompany Site LinkedIn

Location

United States

Posted

110 days ago

Salary

$77K - $95K / year

Bachelor Degree2 yrs expEnglish

Job Description

• Develop high-quality scientific and medical content, including manuscripts, literature reviews, abstracts, posters. • Write clinical study reports, protocols, investigator brochures, regulatory documents (e.g., IND, NDA, EMA submissions). • Produce medical education and promotional materials, patient-friendly materials, and website content. • Analyze and interpret clinical data to ensure accuracy and scientific integrity. • Conduct literature searches and stay current with scientific developments in relevant therapeutic areas. • Collaborate with cross-functional teams, including medical affairs, regulatory, clinical operations, and subject matter experts. • Ensure all deliverables comply with industry guidelines, regulatory requirements, and internal quality standards. • Manage multiple projects, including timelines, revisions, and stakeholder communication.

Job Requirements

Bachelor’s, Master’s, PharmD, PhD, MD, or other advanced degree in a life science or health-related field.
2+ years of experience as a medical writer (regulatory, clinical, scientific, or medical communications).
Excellent written and verbal communication skills with demonstrated ability to simplify complex concepts.
Strong understanding of clinical research, biostatistics, and scientific methodology.
Proficiency with literature databases (e.g., PubMed), referencing, and citation tools.
Ability to work independently in a remote environment with minimal supervision.
Prior experience in regulatory writing, medical communications agencies, or pharmaceutical/biotech industries (preferred).
Knowledge of AMA style, ICH guidelines, GxP standards, and regulatory documentation requirements (preferred).
Experience writing for multiple therapeutic areas (preferred).
Familiarity with project management tools (e.g., Asana, Jira, Monday.com) (preferred).