Meet is working with a mid-sized biopharma that is focusing on discovering and developing innovative medicines in areas of high unmet medical need. My client is looking to bring on Clinical Trial Managers that will manage all components of clinical trials as independently as possible and within timelines and budgets.
My client has a product pipeline of new investigational drugs that includes treatments for cancer, auto-immune disease and chronic pain. The company also has several strategic partnerships ranging from joint discovery, co-development to licensing, and royalty arrangements with numerous companies.
-Oversee/manage all aspects of trials in accordance with SOPs, ICH/GCP regulations
-Assist in identification, evaluation, hiring, and management of CROs and other third party vendors
-Write or contribute to preparation of clinical protocols, informed consent forms, study manuals, care report forms, and other related documents
-Lead/participate in functional initiatives and/or activities as assigned – may also mentor and develop junior clinical operations staff
-Bachelor’s degree or equivalent with 8 years pharma development experience
-2 years’ experience trial management oversight required
-Thorough knowledge of clinical monitoring practices required
Contact Juliette Leite at email@example.com // 628-229-9026 if you are interested in finding more about this position. This will be 100% confidential.
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