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MMS is an innovative, data-focused CRO that supports the pharmaceutical, biotech, including clinical trial transparency,and medical device industries with a proven, scientific approach to complex trial data and regulatory submission challenges. Strong industry experience, technology-enabled services, and a data-driven approach to drug development make MMS a valuable CRO partner, creating compelling submissions that meet rigorous regulatory standards. With a global footprint across four continents, MMS maintains a 97 percent customer satisfaction rating, and the company has been recognized as a leading CRO inGlobal Health & Pharma’sinternational awards programs for the last three consecutive years. For more information, visit www.mmsholdings.com or follow MMS on LinkedIn.
Responsibilities
Requirements
Full Time
$80k-108k (estimate)
06/24/2024
05/25/2026
mmsgroup.com
AMSTERDAM, NY
<25
Private
VIOLET WALKER
<$5M
The job skills required for Principal Medical Writer include Clinical Trial, Drug Development, Word Processing, Customer Satisfaction, Presentation, PowerPoint, etc. Having related job skills and expertise will give you an advantage when applying to be a Principal Medical Writer. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Principal Medical Writer. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Principal Medical Writer positions, which can be used as a reference in future career path planning. As a Principal Medical Writer, it can be promoted into senior positions as a Medical Writer III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Principal Medical Writer. You can explore the career advancement for a Principal Medical Writer below and select your interested title to get hiring information.