You will be responsible for the internal and external coordination of development work toward GMP production of RNA preparations and correspondingly also supervise the activities...
PPD - Pharmaceutical Product Development
Cambridge or Home Based, United Kingdom
Working on behalf of major pharmaceutical, biotechnology and medical device companies in support of clinical trials, you will liaise closely with our statisticians, programmers,...
Posted 1 day ago
Responsible for providing complex medical information for the assigned therapeutic area(s) and serving as a liaison to medical information colleagues within AbbVie regions and...
Posted 3 days ago
The Clinical Research Manager (CRM) will provide leadership, mentorship; training and career development for assigned Clinical Research Associates (CRAs) and/or Project Managers...
Posted 8 days ago
Perform all clinical monitoring/site management activities for assigned projects in accordance with PAREXEL's standard operating procedures; Conduct qualification visits (QV), site...
Posted 16 days ago
Harefield, United Kingdom
The Principal Regulatory Affairs Executive is responsible for preparing high quality documentation for all regulatory submissions, primarily medicinal products, with minimum...
Posted 34 days ago
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