A Clinical Study Manager opportunity is available in Irvine, CA courtesy of Adecco Medical and Science. This person
will be responsible for ensuring that clinical strategies are converted into operational plans and executed accordingly.
This professional will have proficiency/experience in:
Clinical data management documentation
Study management (site monitoring preferred)
Solid GCP, ICH, PhRMA guidelines
PhD/PharmD/MD/OD with 4 years' pharma experience (preferably clinical research) OR
Master's degree with 7 years' pharma experience (with 4 years of clinical research) OR
Bachelor's degree with 9 years' pharma experience (with 6 years of clinical research)
If you have a solid background in clinical practices and procedures, scientific methods, and human medical research,
please email a resume to email@example.com and call Scott Shuman at 585.613.3028.
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