Sr. Medical Writer (Remote) Greenwich Biosciences, Inc United States

  • Full Time
  • United States
  • Applications have closed

Website Greenwich Biosciences, Inc

If you are looking for excellent opportunities near United States then apply for Sr. Medical Writer (Remote). This new opportunity is offered by Greenwich Biosciences, Inc in their local office. Extended application deadline approaching.

Brief Details

Job: Sr. Medical Writer (Remote)


Company: Greenwich Biosciences, Inc
Location: United States

Job Description

We are looking for enthusiastic and talented individuals who thrive on challenge and change, and who want to make a difference through the delivery of results.

About the Role

Contribute directly to scientific communication deliverables in support of our research in disorders of the central nervous system (CNS), with a focus on epilepsy. This involves organizing, analyzing, and interpreting complex medical, scientific, and/or technical data to produce clear and cogent scientific publications (manuscripts, abstracts, slides, posters). The position may also oversee work done by agency/freelance medical writers and less experienced members of internal team.


Participate in strategic publication planning activities and execute on publication plan to produce a full range of written communication with considerations for the target audience including the planning, preparation, writing, reviewing, editing, formatting, QC, and submission of external scientific publications (abstracts, posters, slides, and manuscripts) for marketed products and compounds in development
Contribute to and collaborate on statistical analyses and data quality checks for complete results interpretation demonstrating advanced problem solving ability.
Proactively collaborate with all relevant parties (biostatistics, clinical operations, project management, medical affairs, pharmacovigilance, regulatory, quality assurance, manufacturing, and commercial) and manage projects to external and internal timelines and deadlines.
Manage agency/freelance medical writing projects and review work done by internal team members
Contribute to medical writing process development and process improvement initiatives
Ensure compliance, remain informed on regulations and developments in medical writing, and maintain knowledge of product areas, current trends, and current literature.

PhD/PharmD with extensive writing experience including 3+ years industry medical writing or BS in life sciences field with 6+ years of industry medical writing experience
Successful completion of medical writing training programs (eg, AMWA) and/or applicable certification
Experience in the central nervous system (CNS) therapeutic field highly preferred
Comprehensive knowledge of GCPs, ICH guidelines, and FDA regulations; knowledge of the drug development process.
Strong understanding and comprehension of medical terminology, with the ability to interpret and present scientific and clinical trial data and understand statistical methods and analysis plans.
Excellent writing/editing skills coupled with expertise with Datavision (highly preferred) publication tracking software, Endnote (or equivalent), MS Office (Word, Excel, Access, PowerPoint), scientific search engines (PubMed, Google Scholar), image production software (Photoshop), and online journal/conference submission systems. Knowledge of InDesign and basic elements of graphic design is a plus.
Proven ability to work independently and under constant deadlines; able to work in a quickly changing, not fully structured internal and external environment.
Demonstrated ability to appropriately handle highly sensitive and confidential situations and matters with faculty and staff.
Detail-oriented, with good organizational, prioritization, communication, and time management proficiencies.
***NOTE : Please submit relevant writing samples: abstracts, posters, slides, and manuscripts for consideration.

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