Depending on experience responsibilities include:
* All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
* All aspects of site and registry management as prescribed in the project plans
* Organize and make presentations at Investigator Meetings
* Report, write narratives and follow-up on serious adverse events ...
Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry knowledge, experience, and proven processes. Our goal is to provide the information our clients need to deliver safe, effective and quality products and services every time.
A Validation Engineer at ProPharma ...
Below is a template job description. Every clients job description is a little different.
License/Certification/Education: Normally a B.A./B.S. in Biology and meet all licensing requirements w/1-3 years of experience.
Performs laboratory tests and analyses according to established procedures in designated technical department. Evaluates procedures and methods under direct supervision of more senior technologist, department supervisor, or group leader. Assists in ...
Oct 20 -
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