Job Search Results - Biospace
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2/10/2016
Lab Support, A Division Of On Assignment
Grafton vicinity, MA

BASIC SUMMARY: Perform preparation of routine to complex test article/substance dosage solutions. Act as primary technician for multiple complex studies simultaneously. Assist department management with oversight and daily supervision of...

2/10/2016
Lab Support, A Division Of On Assignment
Beverly vicinity, MA

Lab Support, a scientific staffing firm, is currently recruiting for a Principal Scientist/Technical Lead to work on-site in the north shore area. Description: Scientist: Companion Diagnostics An opening exists for a scientific leader within our...

2/10/2016
PAREXEL International
Waltham, MA

Home-based Clinical Regulatory Medical Writer opportunities in the US and Canada! PAREXEL is one of the largest providers of medical writing services worldwide and has managed thousands of writing projects in more than 29 countries in North and...

2/10/2016
Zintro
Cambridge, MA

Zintro is looking for candidates on behalf of our client. We are seeking a Quality Systems Specialist for a Full-time position based in Cambridge, MA. ***To be considered for this job, Candidates MUST reply with a brief summary of their...

2/10/2016
Zintro
Southborough, MA

Zintro is looking for candidates on behalf of our client. This is a full-time employment opportunity onsite in Southborough, MA.**As a Manager, Clinical and Regulatory Medical Writing You Will:- Implement project-specific strategies and...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Role:1. Act as liaison between the in-country International RA Team and GRA in Lexington for any CMC and Quality/Regulatory compliance related issues and projects 2. Liaise between the CMC GRA team members and international regulatory leads...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleThe individual will be a key contributor within a group responsible for performing purification process development, including timely completion of small-scale experiments, scale-up, technology transfer and GMP floor support for programs...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary RoleUnder the direction of the line manager, the Associate Director is responsible for supporting the oversight and management of the Global CMC Regulatory Submissions for Development submissions (IMPD/CTA/IND), Marketing Applications (NDA,...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Role:* Work with the Global Medical Team leader , neuroscience to develop and execute multi-year global medical strategy for the specified Product/Disease Area, appropriately aligned with overall strategy and incorporating R&D functional...

2/10/2016
Shire Pharmaceuticals Group
Lexington, MA

Primary Duties: 1. Act as liaison between the in-country International RA Team and GRA in Lexington for any CMC and Quality/Regulatory compliance related issues and projects 2. Liaise between the CMC GRA team members and international regulatory...