Medical Writer-Clinical & Regulatory-US Pharmaceutical Co-Miami, FL Area

Medical Writer-Clinical & Regulatory-US Pharmaceutical Co-Miami, FL Area

 

Position Summary

An attractive opportunity to join a US Pharmaceutical Company with multiple FDA approved drugs and an attractive development pipeline that is also located in a high ?quality of life? location, i.e. the Miami, Florida area. Compensation for this Medical Writer position will vary depending upon the depth and quality of relevant Clinical & Regulatory Medical Writing experience, and the base salary will vary from $90k to $100k, and this position is also eligible for an annual bonus and an attractive benefits package too.  All inquiries and submissions are held in strict confidence (see our privacy policy below).


Company Description:

A young, successful, expanding and fully integrated Pharmaceutical Company (i.e. discovery, development, manufacturing and commercialization). 


Location: Miami, Florida area

 

Relocation Assistance: Relocation assistance is available for qualifying candidates.

 

Compensation: Total compensation will vary depending upon depth and quality of relevant Clinical & Regulatory Medical Writing experience, base salary will range from $90k to $100k, and this position is also eligible to receive an annual bonus and attractive benefits too.

 

Attractive features about this position/opportunity, and Company:Highly visible position Gain valuable global clinical research experience  Chance to make an impact and a real difference Join a young & successful company with multiple FDA approved drugsJoin a company with FDA approved drugs and an attractive pipeline too.Enjoy an attractive & extensive benefits package that includes, but is not limited to, 3 weeks vacation, an additional week off between Xmas and New Year?s Day, bonus, employee stock purchase plan, 401k plan and more. Live and work in a very attractive ?quality of life? location, i.e. the Miami area 

 

ResponsibilitiesThis Medical Writer position will include, but will not be limited to, being involved or responsible for writing the following: Clinical protocols and amendmentsPortions of IND submissions  Portions of NDS submissions (note: using CTD format)Clinical Study ReportsInvestigative Brochures

 

This position will also involve working closely with clinical research, clinical operations, regulatory affairs, medical affairs, biostatistics and others. 

 

RequirementsAn advanced degree is highly preferred (i.e. MD, PhD, PharmD, MSN), however strong and relevant Clinical & Regulatory Medical Writing experience is most importantFive or more years of Clinical Research experience (7 or more years of Clinical & Regulatory Medical Writing experience is a big plus) gained working in industry for a Pharmaceutical company, a Biopharmaceutical company and/or a CRO.

 

Cornerstone?s Privacy Policy
Cornerstone Search Group considers all inquiries, resume submissions, and any other personal information submitted to us as confidential information. This information will not to be shared with any parties outside of Cornerstone Search Group without your prior permission.

Contact:  
Cliff Miras (initial contact via email works best)

Co-founder & Managing Partner

 

Cornerstone Search Group, LLC
9 Sylvan Way
Parsippany, NJ 07054
P 973-656-0220 ext 11
F 973-656-0228
cmiras@cornerstonesg.com
Web/URL: www.cornerstonesg.com

About Cornerstone Search Group, LLC
CORNERSTONE is a specialty pharmaceutical recruiting firm.  We help our clients hire experienced pharmaceutical professionals from the Staff through Management (VP/Director) levels for Full-Time positions and Contract assignments.