Clinical Data Manager II California
1/10/2017 10:17 AM

The Clinical Data Manager II (CDM II) will provide oversight of, assist in the coordination of, and/or partake directly in the data management activities from study start-up, data processing, and database close-out in a paper or electronic environment for projects sponsored by DNS where the activities are conducted in-house or by CROs. The ideal candidate will have advanced knowledge of clinica  ...View Job
Associate Scientist III, Lead Discovery California
12/19/2016 11:21 AM

Dart Neuroscience LLC is seeking an Associate Scientist with experience in molecular and cellular biology, assay development, and small molecule screening to join the Lead Discovery group. DNS is a highly interactive company and the ability to communicate effectively with colleagues and the desire for collaborative teamwork are vital for success in this role. The primary responsibilities of thi  ...View Job
Associate Scientist, Medicinal Chemistry California
12/12/2016 10:55 AM

The successful Associate Scientist candidate will be an accomplished synthetic/medicinal chemist with state of the art knowledge of synthetic organic chemistry and will be a motivated, creative, hands-on laboratory scientist with the ability to interact effectively with team members in all areas of drug discovery. Major responsibilities will involve the design, synthesis, purification and characte  ...View Job
Scientific Computing Engineer III California
11/29/2016 8:48 AM

The successful candidate will have deep knowledge of project management for software systems in the Pharmaceutical/Biotech Industry. This will include (1) use-case / requirements gathering from scientific end-users and the ability to translate these requirements to enable Scientific Computing deliver the best solutions possible in the most efficient manner, (2) ability to track requirements and b  ...View Job
Clinical Research Associate I/II California
11/22/2016 9:00 AM

• Administration and site level responsibility for clinical studies according to DNS Standard Operating Procedures, ICH Guidelines and GCP. • Work as part of the DNS Project Team to contribute towards the management and execution of DNS Clinical Programs. • Monitor study progress and milestones. Responsibilities • Conduct pre-study, initiation, routine monitoring and closeout visits of stu  ...View Job
Manager/Senior Manager, Regulatory Affairs California
11/7/2016 11:37 AM

Working in a team environment, the Regulatory Affairs Manager/Senior Manager will be responsible for executing regulatory strategy as well as hands-on management of all technical and operational aspects related to the regulatory lifecycle (e.g., from preclinical candidate designation through registration) of assigned DNS products. Strategic Planning • Represent the Regulatory Affairs dep  ...View Job
Associate Director, Regulatory Affairs California
11/4/2016 3:19 PM

Working in a team environment, the Regulatory Associate Director will be responsible for development of regulatory strategy as well as hands-on management of all technical and operational aspects related to the regulatory lifecycle (e.g., from preclinical candidate designation through registration) of assigned DNS products. Strategic Planning • Represent the Regulatory Affairs department on  ...View Job
Scientist, Structural Biology California
11/3/2016 9:05 AM

DNS is seeking an experienced protein chemist for the structural biology department. The candidate will be responsible for the development and implementation of protein purification processes for macromolecular crystallography studies as well as for biochemical/biophysical assay development and screening. The candidate is also required to have an extensive technical background in state-of-the-ar  ...View Job
Clinical Biostatistician California
8/23/2016 10:09 AM

The Clinical Biostatistician (BS) provides overall statistical leadership, direction, and consulting to the Biostatistics, Statistical Programming, Data Management, Clinical R&D and Regulatory Affairs functions relating to the design, analysis and reporting of clinical trials in support of Phase I-IV clinical development and regulatory submission programs. This highly visible role will activel  ...View Job