Sr Medical Writer

Job Opening for Sr Medical Writer, Overland, KS - Remote
We are currently working on below mentioned job opening i.e Job Opening for Sr Medical Writer, Overland, KS - Remote. Please let me know if you are interested in applying for the same.

Job Title: SR Medical Writer X4
Location: Overland, KS - Remote
Length of Assignment: 12 months
 
Looking for Medical Writers with protocol writing for drug and biologic trials.
Writers will be assigned to one or two product teams and then assigned documents that need to be completed.  The company has templates in place for the documents, but the consultant will have to take full ownership of the document and will have to work cross functionally with the 9-12 individuals that will be assigned to each product.  They have product in various stages from preclinical to phase III of which most are on the small molecule or drug side. 
Filling out the excel spreadsheet will be key with each submittal as it is required by the manager to assess where their strengths are for each writer. 
 
Main documents that will be assigned are:
CSRs
Protocol Development
Clinical protocol synopses (Ph.1-3)
Clinical protocols (Ph.1-3)
Must:
Drug Backgrounds
Medical Writing in all areas outlined in responsibilities
 
Cultural fit is important to the end client:  consultant will need to be Assertive, Confident, Adaptable, Timely and responsive throughout the day, Be able to handle pressure as it can be an intense environment at times.

Job Opening for Sr Medical Writer, Overland, KS - Remote
We are currently working on below mentioned job opening i.e Job Opening for Sr Medical Writer, Overland, KS - Remote. Please let me know if you are interested in applying for the same.

Job Title: SR Medical Writer X4
Location: Overland, KS - Remote
Length of Assignment: 12 months
 
Looking for Medical Writers with protocol writing for drug and biologic trials.
Writers will be assigned to one or two product teams and then assigned documents that need to be completed.  The company has templates in place for the documents, but the consultant will have to take full ownership of the document and will have to work cross functionally with the 9-12 individuals that will be assigned to each product.  They have product in various stages from preclinical to phase III of which most are on the small molecule or drug side. 
Filling out the excel spreadsheet will be key with each submittal as it is required by the manager to assess where their strengths are for each writer. 
 
Main documents that will be assigned are:
CSRs
Protocol Development
Clinical protocol synopses (Ph.1-3)
Clinical protocols (Ph.1-3)
Must:
Drug Backgrounds
Medical Writing in all areas outlined in responsibilities
 
Cultural fit is important to the end client:  consultant will need to be Assertive, Confident, Adaptable, Timely and responsive throughout the day, Be able to handle pressure as it can be an intense environment at times.