Medical Writer (Global Hub)

Syneos Health; Buenos Aires; Presencial; ARS 97.588.178 - 125.470.514; Jornada completa

Descripción de la vacante

Syneos Health is seeking a Medical Writer to develop evidence-based materials by translating clinical and scientific data into compelling content. This role involves ensuring scientific rigor and quality across publications while conducting literature searches and developing clinical study protocols. Candidates should have a degree with relevant experience, strong writing skills in English, and familiarity with medical literature databases. Join a team where innovation meets excellence in medical communications.

Formación

• Translate clinical and scientific data into accurate content.
• Gather and evaluate scientific literature to ensure accuracy.
• Compiles, writes, edits, and coordinates medical writing deliverables.

Responsabilidades

• Conduct literature searches and evaluate relevance of scientific literature.
• Ensure scientific accuracy & quality of all written materials.
• Support development of clinical study protocols and reports.

Conocimientos

Scientific and clinical writing and expertise

Literature searching & synthesis

Quality control and proofreading

Stakeholder and time management

Familiarity with MS office and medical literature databases

Compliance knowledge

Advanced level of English

Educación

BS + 8 yr experience

MSc/M. Pharm/PharmD + 4 yr experience

PhD + 1 yr experience

3-4 years of clinical research experience

Herramientas

Microsoft Office (Word, Excel, PowerPoint)

Medical literature databases (e.g., Ovid, Medline, PubMed)

Descripción del empleo

The Medical Writer is responsible for developing clear, evidence-based materials by translating clinical and scientific data into accurate, compelling content. Working with internal teams, the role ensures strategic alignment, scientific rigor, and quality across publications and materials.

Key Skills Required:

• Scientific and clinical writing and expertise
• Literature searching & synthesis
• Quality control and proofreading
• Stakeholder and time management – ability to develop rapport with others and work in a team environment
• Familiarity with MS office and medical literature databases
• Compliance knowledge – familiarity with SOPs, audit requirements, and training standards within medical fields
• Advanced level of English; strong oral/written communication skills in English

Key Responsibilities:

• Research and Analysis – Gather and evaluate scientific literature to ensure the accuracy and relevance of information used in medical comms. Conduct literature searches using PubMed and other scientific databases, evaluating & validating references for accuracy/applicability.
• Content Development – Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately. Support the summarization and referencing of learning objectives to ensure clarity and alignment with educational goals.
• Clinical Study Protocol – Supports completion of clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures, NDA and eCTD submissions; journal manuscripts; and abstracts, posters, and presentations for scientific meetings.
• Quality Assurance – Ensure the scientific accuracy & quality of all written materials and adherence to regulatory, internal, and client‑direct standards/specifications. Support MLR processes to ensure compliance and QA. Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format.

Key Metrics to Monitor:

• Content Quality & Effectiveness - Quality score as per a pre‑determined quality scorecard on writing deliverables.
• On‑Time Delivery Rate – Deliverables submitted by agreed milestones.
• Feedback Scores – Quality feedback from senior medical writers or reviewers.

Additional Responsibilities:

• Off‑the‑shelf Training Management – Partner with teams to create and summarize inventories of existing assets. Assist in developing, updating and maintaining role‑specific/ disease‑specific training programs/curricula.
• Transcripts for e‑Learning – Support preparation of transcripts for conversion into e‑modules and other training modalities.
• Regulatory & Industry Compliance - Maintains familiarity with current industry practices and regulatory requirements and guidelines that affect medical writing.
• Budget Management - Maintains awareness of budget specifications for assigned projects, working within the budgeted hours and communicating changes to medical writing leadership.

Qualifications:

• BS + 8 yr experience; MSc/M. Pharm/PharmD + 4 yr experience; PhD + 1 yr experience
• 3-4 years of clinical research experience
• Working knowledge of Microsoft Office software (Word, Excel, and PowerPoint)
• Working knowledge of medical literature databases (e.g., Ovid, Medline, PubMed, etc.)

Syneos Health companies are affirmative action/equal opportunity employers (Minorities/Females/Veterans/Disabled).

Syneos Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, age, religion, marital status, ethnicity, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability or any other legally protected status and will not be discriminated against. If you are an individual with a disability who requires reasonable accommodation to complete any part of our application process, including the use of this website, please contact us at: Email: [emailprotected] One of our staff members will work with you to provide alternate means to submit your application.