- Abbott (Santa Clara, CA)
- …colleagues serve people in more than 160 countries. **Job Title** **Sr. Scientist Clinical Research ** **About Abbott** Abbott is a global healthcare leader, ... as well as study sites as directed by your manager . **What You'll Work On** + Writes clinical...literature, analyzing scientific data and staying abreast of current clinical practice. + Facilitates regulatory submissions and… more
- Abbott (Sylmar, CA)
- …provide directives to teams as well as study sites. Be able to mentor other clinical scientists within Clinical Research . **What You'll Work On** + Provide ... treat people with heart arrhythmias, or irregular heartbeats. **Senior** **Principal** ** Clinical ** ** Research ** **Scien** **tist** **,** will be viewed as… more
- Actalent (Modesto, CA)
- Clinical Research Coordinator Job Description We...expertise + Clinical trial management + Good Clinical Practice (GCP) + IRB knowledge + Regulatory ... are seeking an experienced Clinical Research Coordinator with a minimum of...site, working alongside a nurse lead. Responsibilities + Perform regulatory tasks, including IRB submissions. + Engage in sponsor… more
- Terumo Neuro (Aliso Viejo, CA)
- **12869BR** **Title:** Clinical Research Assoc, Sr. **Job Description:** Responsible for coordinating clinical research activities in accordance with ICH ... address and resolve queries. + Work closely with Project Manager (s) to ensure clinical studies are conducted...related field. 2. Minimum six (6) years of direct clinical research experience, preferably in the medical… more
- Abbott (Alameda, CA)
- …+ BS degree in life sciences or equivalent with minimum 5 years of clinical research experience + Must have 2+ years of relevant experience in ... for completeness and accuracy, and escalate issues to the Clinical Operations Manager as needed. + Participate...flexible when priorities change. + Working knowledge of GCP, Clinical and Regulatory Affairs. + Proficient with… more
- Actalent (Merced, CA)
- …reporting. Process laboratory specimens per study requirements. Qualifications 3-5 years of Clinical Research Coordinator Experience with clinical ... Description Position Overview The CRC collaborates with the Research Institute Division Manager , Principal Investigators,...and key stakeholders to plan, coordinate, implement, and complete clinical trials and research projects. You will… more
- Actalent (Santa Maria, CA)
- The Clinical Research Nurse collaborates with the Research Institute Division Manager , Principal Investigators, and key stakeholders to plan, coordinate, ... PI and healthcare team. Ensure compliance with study protocols, regulatory requirements, and ethical standards. Coordinate study activities from...Oncology experience Must have a minimum of 3 of Clinical Research Nurse experience Must hold an… more
- Stanford University (Stanford, CA)
- … Manager to provide leadership and oversight of a significant number of clinical research projects, with an emphasis on supervising, evaluating, and training ... Research Nurse Manager **School of Medicine,...research staff. Responsible for managing clinical research operations, applying medical knowledge and… more
- Abbott (Sylmar, CA)
- … regulatory guidelines, policies and regulations + Ethical guidelines of the regulatory profession, clinical research and regulatory process ... Management solutions The Opportunity - We are seeking a Regulatory Affairs Project Manager to join our...applicable reports and ensure appropriate responses are submitted to regulatory authorities + Evaluate proposed preclinical, clinical … more
- BeOne Medicines (Emeryville, CA)
- …with general and study-specific monitoring issues * Provide direct support to the Clinical Study Manager by assisting with monitoring visit report review and ... site monitor and is responsible for the management and oversight of their assigned clinical study sites to ensure data quality and patient safety in accordance with… more