- AbbVie (South San Francisco, CA)
- …integrity, and review, interpretation, and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as… more
- ThermoFisher Scientific (San Diego, CA)
- …high EQ important + Thorough understanding of overall biologic/ pharmaceutical product development process from pre-clinical through post-marketing, including ... one or more therapeutic areas and one or more drug classes. + Deep knowledge of clinical program and...knowledge of clinical program and study design, relevant endpoints, safety considerations and current regulatory and commercial landscapes. +… more
- CTG (Woodland, CA)
- …USDA on regulatory compliance, including approvals, import/export compliance, traceability, quarantine, safety testing, and affidavits * Serve as a resource for ... 3 years' experience in Quality or Regulatory, preferably in medical device, pharmaceutical , or biotechnology industries * Strong knowledge and application of Quality… more
- AbbVie (Irvine, CA)
- …integrity and review, interpretation and communication of accumulating data pertaining to safety and efficacy of the molecule. Along with Clinical Operations, is ... the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. Serves as… more
- ICON Clinical Research (Los Angeles, CA)
- …track site staff training and maintain compliance records + Monitor patient safety , ensuring timely and accurate AE/SAE/PQC reporting + Support subject recruitment ... and retention efforts at the site level + Oversee drug accountability and ensure proper storage, return, or destruction + Resolve data queries and drive timely,… more
- Gilead Sciences, Inc. (Foster City, CA)
- …in shaping clinical strategy, collaborating cross-functionally with research, regulatory, safety , and commercial teams to advance innovative therapies that address ... MD (or equivalent medical degree) and 4 years' clinical, scientific and/or drug development experience in the biopharma industry, healthcare, consulting, academia or… more
- Datavant (Sacramento, CA)
- …RWE in the pharmaceutical and life sciences space + Understanding of drug development and/or clinical trials \#LI-BC1 We are committed to building a diverse team ... including variable pay) for this role is: $125,000-$150,000 USD To ensure the safety of patients and staff, many of our clients require post-offer health screenings… more
- Enviri Corporation (San Jose, CA)
- …work culture that fosters growth and development while ensuring the health and safety of our employees. Why join Clean Earth? In addition to competitive pay, ... or more years of experience in lab packing, segregating pharmaceutical waste, chemical service specialist or as a truck...contingent upon successful completion of a DOT physical, DOT Drug Screen and any other DOL or company requirements.**… more
- ManpowerGroup (San Fernando, CA)
- Our client, a leading organization in the pharmaceutical industry, is seeking a Chem Tech I to join their team. As a Chem Tech I, you will be part of the Quality ... to detail, excellent analytical skills, and a commitment to safety , which will align successfully in the organization. **Job...period associates are eligible for:** + Medical and Prescription Drug Plans + Dental Plan + Supplemental Life Insurance… more
- AbbVie (South San Francisco, CA)
- …organization. Specific areas of work may include clinical trials, patient safety , and global medical affairs. The Manager works independently in partnership ... drive innovation by raising the bar and challenging the status quo + Pharmaceutical or related industry knowledge desired, including experience and understanding of … more