Medical Writer / Sr Medical Writer - Gaithersburg, MD | Biospace
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Medical Writer / Sr Medical Writer

MedImmune, LLC

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Location:
Gaithersburg, MD
Posted Date:
1/20/2017
Position Type:
Full time
Job Code:
R-002396
Salary:
Required Education:
Doctorate/PhD
Areas of Expertise Desired:

Job Description

                             
                                       Location:Gaithersburg, United States
Cambridge, United Kingdom
Job reference: R-002396

Posted date: Jan. 17, 2017



 

   If you’re inspired by the possibilities of science to change lives and you thrive when making brave decisions – join us.  

   MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease.  As a Medical Writer / Sr Medical Writer in either Gaithersburg, MDor Cambridge, UK, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.  

   We’re constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We’re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we’re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as part of the AstraZeneca family, as together we explore synergies between small and large molecules.  

   MedImmune has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent.  

   Main Duties and Responsibilities  

   As Medical Writer / Sr Medical Writer, you will be responsible for assisting in the development of high-quality clinical regulatory and other supporting documents for pipeline and/or marketed products as well as assisting in the development of high-quality clinical abstracts, posters, and manuscripts. You will work under direct supervision to manage and prioritize workload to ensure deliverables are completed per time and quality goals.  

   Additionally you will be assisting in the writing/editing of clinical regulatory and other supporting documents for assigned studies/indications, and assisting in the management of the overall development and approval process. You will also assist in the analysis, synthesis, and presentation of complex information, provide QC review support as needed, and assist in the writing of clinical abstracts, posters, and manuscripts for assigned studies.  

   NOTE: This position can be filled in either Gaithersburg, MD or Cambridge, UK.  

Requirements

   Essential Requirements  

   For Medical Writer:  

 
       
  •      PhD/PharmD in a scientific discipline, or a Master's degree with relevant experience    
  •    
  •      1-2 years of experience in the medical/regulatory/publication writing field in the pharmaceutical/biotech industry or CRO environment.    
  •  

   For Senior Medical Writer:  

 
       
  •      PhD/PharmD in a scientific discipline, or a Master's degree with relevant experience    
  •    
  •      2-4 years of experience in the medical/regulatory/publication writing field in the pharmaceutical/biotech industry or CRO environment.    
  •  
   Desirable Requirements    
       
  •      High attention to detail    
  •    
  •      Authoring/editing CSRs and other types of clinical regulatory documents (eg, clinical protocols, Investigator's Brochures) or scientific publications including abstracts and posters.    
  •    
  •      Knowledge of Microsoft Office applications and electronic document management systems    
  •    
  •      Knowledge of the drug development process and principles of GXP/ICH/CTD and other global standards, with an understanding of the basic strategy for regulatory submissions. Background in biologics.    
  •    
  •      Willingness or ability to work collaboratively and coordinate the efforts of team members to resolve comments and complete deliverables.    
  •    
  •      Strong written, verbal, and interpersonal communication skills.    
  •    
  •      Willingness or ability to manage/prioritize multiple projects under general supervision, working in a fast-paced environment.    
  •    
  •      Flexible/willing to adapt to changing deadlines and priorities.    
  •  

   Next Steps – Apply today!  

 

   To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.  

   AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.  

   ~bsp  

 

   *LI-MEDI