parexel senior medical writer内推
23440
大家好，目前parexel International在招聘 senior medical writer,
要求：
Home-based Clinical Regulatory Medical Writers in the US and Canada
As a PAREXEL Medical Writer, you will be exposed to different project teams, as well as a diverse portfolio of clients. The ability to understand our clients’ needs and achieve quality results is critical for us to continue to be one of the best clinical research organizations (CROs) in the world. To accomplish this, we believe that you must have the power to work independently and intelligently every day.
You will:
;Write and edit clinical study documents.
;Act as the primary client contact for medical writing projects.
;Partner with sponsors to deliver quality documents on time.
;Mentor and train junior medical writing staff.
Qualifications
Our ideal candidate has:
;Extensive experience writing clinical study reports, eCTD documents or similar, or protocols for Early Phase, Phase II or Phase III trials.
;Demonstrated understanding of clinical research, the drug development process, and applicable regulatory guidelines.
;The ability to manage multiple and varied tasks with enthusiasm and to prioritize your work while paying attention to details.
;A bachelor’s degree in Life Sciences/Health-Related Sciences or equivalent experience.
;Fluency in written and spoken English.
有兴趣的请发简历和cover letter到 1point3acres.com
我可以帮忙内推。谢谢！
要求：
Home-based Clinical Regulatory Medical Writers in the US and Canada
As a PAREXEL Medical Writer, you will be exposed to different project teams, as well as a diverse portfolio of clients. The ability to understand our clients’ needs and achieve quality results is critical for us to continue to be one of the best clinical research organizations (CROs) in the world. To accomplish this, we believe that you must have the power to work independently and intelligently every day.
You will:
;Write and edit clinical study documents.
;Act as the primary client contact for medical writing projects.
;Partner with sponsors to deliver quality documents on time.
;Mentor and train junior medical writing staff.
Qualifications
Our ideal candidate has:
;Extensive experience writing clinical study reports, eCTD documents or similar, or protocols for Early Phase, Phase II or Phase III trials.
;Demonstrated understanding of clinical research, the drug development process, and applicable regulatory guidelines.
;The ability to manage multiple and varied tasks with enthusiasm and to prioritize your work while paying attention to details.
;A bachelor’s degree in Life Sciences/Health-Related Sciences or equivalent experience.
;Fluency in written and spoken English.
有兴趣的请发简历和cover letter到 1point3acres.com
我可以帮忙内推。谢谢！
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