Navitas is Growing

Great work begets more work, and Navitas Life Sciences is growing. Would you like to work on projects with world class global Life Science companies?

August 03, 2015, Princeton, New Jersey:Navitas Life Sciences is Growing

Great work begets more work, and Navitas Life Sciences is growing. Would you like to work on projects with world class global Life Science companies? Our clients are in the pharmaceutical, biotech and medical device industries, and we have opportunities in New Jersey, Massachusetts and California.

New Jersey opportunities include SAS Programmers with 8 or 9 years’ experience supporting clinical trials for regulatory submissions, Medical writers with 5 years’ experience preparing medical writing documents, Biostatisticians with advanced knowledge of clinical database design, and Clinical data managers that will lead DM study start – ups.

A project manager is needed in Massachusetts that will be working directly within our client and will be responsible for global licensing and registration inform action process.

In California a Research Associate that should demonstrate a strong background in molecular biology techniques (Molecular Cloning, qRT – PCR, transfections, etc.) cell and tissue culture, immunoassays, and more.

If you believe you are a fit for any of these opportunities, send your resume to This email address is being protected from spambots. You need JavaScript enabled to view it.

To view more opportunities, visit http://www.navitas.net/index.php/2014-08-06-06-53-37/careers/opportunities/postings

 

August 03, Princeton, New Jersey:Navitas Life Sciences is Growing

Great work begets more work, and Navitas Life Sciences is growing. Would you like to work on projects with world class global Life Science companies? Our clients are in the pharmaceutical, biotech and medical device industries, and we have opportunities in New Jersey, Massachusetts and California.

New Jersey opportunities include SAS Programmers with 8 or 9 years’ experience supporting clinical trials for regulatory submissions, Medical writers with 5 years’ experience preparing medical writing documents, Biostatisticians with advanced knowledge of clinical database design, and Clinical data managers that will lead DM study start – ups.

A project manager is needed in Massachusetts that will be working directly within our client and will be responsible for global licensing and registration inform action process.

In California a Research Associate that should demonstrate a strong background in molecular biology techniques (Molecular Cloning, qRT – PCR, transfections, etc.) cell and tissue culture, immunoassays, and more.

If you believe you are a fit for any of these opportunities, send your resume to This email address is being protected from spambots. You need JavaScript enabled to view it.

To view more opportunities, visit http://www.navitas.net/index.php/2014-08-06-06-53-37/careers/opportunities/postings