Health Care

applicants

You have a Masters of Science degree in a bioscience area, Nursing or a Pharm.D.  You have at least five (5) years of pharmaceutical industry experience, including experience monitoring clinical studies.  You have strong knowledge of GCPs, regulations, and compliance issues - and strong project leadership experience.  You have experience with both domestic clinical trials as well as international clinical trials.    experience; international experience is desirable.  Your colleagues have consistently praised you for your strong interpersonal skills as well as excellent communications skills, written and verbal.  You seek a new opportunity with an organization that is totally committed to upholding the highest ethical standards in all of its scientific and business endeavors to maintain good corporate citizenship, and contribute to human welfare and society through the responsible development of its products.If the above describes you, we would very much like to get to know you.  We seek candidates for the role of Manager | Clinical Research.  In this role you will be responsible for managing the overall operations of a clinical research program, which may involve multiple simultaneous clinical studies of all phases of clinical development (phases 1 - 4).  This will include project planning, budgeting, resource management, preparing and negotiating Clinical Trial Agreements and budgets at each study center.  You will participate in the selection and management of CROs for Data Management/ biostatistics and other vendors (e.g., central laboratory).  You will initiate and track payments made to study sites and vendors.  You will organize and conduct Investigator Meetings and making clinical presentations, etc. Candidates have a Bachelors degree in a bioscience.  Preference will be given to candidates with a Masters degree.  Must have at least five (5) years of pharmaceutical industry experience, including monitoring clinical studies with appropriate knowledge of GCPs and regulations.  Must have project leadership experience.  Must have domestic clinical trial experience; international experience is desirable.  Must have strong knowledge of GCO compliance issues.  Must have excellent interpersonal skills.Competitive compensation and full benefits. This is a great opportunity to work for an organization that develops enhanced and innovative therapeutic products of the highest quality and reliability that optimize patient care, provide economic value, and result from efficient paths to commercialization. It is also an excellent opportunity to work for a company that has been recognized by the San Diego Society for Human Resource Management as exhibiting the most innovative, employee-friendly HR practices that improve employee satisfaction and move the needle toward successful company performance. For more information call 941.739.1400 or submit your resume now by clicking on the web URL below.