- Actalent (San Diego County, CA)
- Job Description The Senior Clinical Trial Associate ( Sr . CTA) is responsible for supporting the daily workflow of clinical operations activities. ... document filing, maintaining study trackers, and oversight of the study-specific electronic Trial Master Files (eTMF). Responsibilities + Serve as a member of the… more
- IQVIA (Carlsbad, CA)
- …Research Associate ! You'll play a pivotal role in monitoring and managing clinical trial sites to ensure compliance with study protocols, regulations, and ... phases as required. Documentation: Ensure all site documents are filed in the Trial Master File (TMF) and Investigator's Site File (ISF) per GCP/ICH and local… more
- IQVIA (Carlsbad, CA)
- …applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement. ... with contracted scope of work and regulatory requirements, ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines. *… more
- Edwards Lifesciences (San Diego, CA)
- …the requirements of the Associate Manager Required + Experience in clinical trial design, indication lead + FDA/EMEA/PMDA submission experience + The ... + Act as core team member/lead biostatistician of assigned clinical trial (s) in US and international/global ...prevention of pollution under their span of influence/control The Sr Manager, Biostatistics Level is lateral to Associate… more