Nurix Therapeutics
Medical Director / Senior Medical Director 5948-306
Brisbane, California, United States · Director
Sponsorship not specifiedDetected 17 days ago
GCPStatisticsBusiness DevelopmentExcelClinical TrialsClinical ResearchPatient CareResearchCommunicationCollaborationPublic SpeakingMicrosoft Office
Stay score
odds of building a lasting career here
37Risky
Cap-exempt (no lottery)0
Sponsors this role80
Entry-level history0
PERM / green-card track0
Lottery odds40
Fits your clock70
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Files H-1B transfers
2 transfer filings in the last year, covering 2 workers. Median labor-condition decision: 8 days. An employer that already files transfers is one that can take over an existing H-1B.
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine's next chapter with a new script to outmatch disease.
- In collaboration with the Medical Monitor and Safety team this role will be responsible for safety oversight of clinical trials.
Responsibilities
- Participate, contribute and/or lead cross-functional clinical development teams with strong ability to work closely with all team members, address study or other program-specific questions.
- Develop the Global Development plan with senior clinical development staff
- Implement Global Development Plan with strategic clinical science support
- Acquire and utilize knowledge of clinical trial design and relevant disease indications to assist in study concept and protocol development.
- Contribute to discussions concerning scientific and procedural aspects of study design.
- Coordinate with departments to produce the final protocol and informed consent documents.
- Contribute to the development of CRFs, data edit checks, patient profile design, ongoing data cleaning (query generation, coding review, SAE reconciliation) and data trend analysis.
- Contribute to statistical analysis plans, table, listing, figure design and the preparation of manuscripts and other presentations of study data, as appropriate.
- Assist in determining the activities to support a project's priorities within functional area
- Support business development activities as needed serving as scientific/subject matter Expert
Nice to have
- Experience in the clinical science role, in an oncology indication for first-in-human and proof of concept studies in small molecules, biologics and/or cell therapy.
- Registrational or Phase 3 study experience is desired.
- In depth understanding of clinical operations and translational medicine.
- Excellent interpersonal and communication skills.
- Able to translate technical concepts into accessible language and direction for the broader study team.
- Excellent attention to detail, collaboration and initiative, with flexibility to adapt to the needs of the organization
- Experienced in Microsoft Office (Excel, Word, PowerPoint, OneNote), and ideally also with job related programs such as Spotfire and Medidata Rave or similar.
- Strong understanding of ICH GCP, as well as general knowledge of industry practices and Standards
Compensation
- Prepare clinical portions of all relevant regulatory filings and meeting packages (INDs, Annual Reports, meeting requests, NDAs, etc.) for US and ex-US Health Authorities.
Benefits
- Read and interpret scientific and medical literature for the use in clinical documents and to assist clinical team decision making.
- Contribute and review medical data review plans, Data Safety Monitoring Board (DSMB)/Safety Review Committee (SRC) charters, and specific sections of study manuals and investigator meeting materials.
- Lead internal clinical data review meetings in conjunction with the medical monitor; lead the data preparation effort for dose escalation meeting, as applicable to study stage.
- Coordinate and manage external medical advisory committees for the study team such as DSMBs and Scientific Steering Committees, in conjunction with the medical monitor.
- Research and summarize published literature for continual learning and to prepare training materials for other clinical team members.
- Address investigator questions regarding protocol and related scientific issues and attend site initiation visits (SIVs), in coordination with the medical monitor.
- Medical monitoring duties may be considered depending on degree (e.g., PharmD, MD or other clinical advanced degree) and previous experience.
Apply directly at Nurix Therapeutics →Create a free account for alerts like thisView Nurix Therapeutics immigration profile
This listing is sourced directly from Nurix Therapeutics's careers page and normalized into a canonical job model.