Clinical Research Medical Writer

Piper Health and Sciences is seeking a Clinical Research Medical Writer in Bethesda, MD to support an established clinical research organization (CRO) with communications and document development activities for ongoing clinical research trials.

Responsibilities of the Clinical Research Medical Writer include:

• Coordinate, attend and lead conference calls and meetings related to clinical trials
• Preparing meeting minutes/action items and distributing these to meeting participants
• Assist in the development of medical, scientific, regulatory documents, SOPs, and miscellaneous documents
• Maintain databases and complete data entry and mining activities
• Perform literature searches and assist in the development of protocols
• Analyze medical research data to prepare study findings and reports
• Prepare meeting minute reports for high-level internal and external stakeholder engagements
  
  

Qualifications of the Clinical Research Medical Writer include:

• 2+ years of health or science-related work experience
• Excellent oral and written communications skills, attention to detail, and organization skills
• Strong command of MS Word and Excel and experience with MS SharePoint preferred
• Bachelor of Science in a science-related field (Public Health, Biology, Health Science, Biological Sciences, Psychology, etc.)
  
  

Compensation for the Clinical Research Medical Writer:

• Salary: $70,000 - $85,000 based on relevant experience
• Benefits: Cigna Health, Dental, & Vision Insurance, 401k Contributions
  
  

Keywords:

CRO, Clinical research organization, clinical trials, pharmaceutical, biotechnology, biotech, gcp, good clinical practices, research assistant, research associate, research program coordinator, clinical research coordinator, clinical research assistant, clinical technician, medical assistant, medical technician, medical scribe, chief scribe, scribe, transcription, meeting minutes, medical writing, scientific writing, grant writing, proposal writing, publication, SAE, serious adverse event, AE, adverse event, protocol development, regulatory binder, regulatory affairs, regulatory, sop, standard operating procedures, protocol, quality assurance, qa, capa, investigations, physiology, pharmacology, public health, science writer, science writing