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The Cedars -Sinai F. Widjaja Foundation Inflammatory Bowel and Immunobiology 
Research Institute (IBIRI) is searching for a highly motivated Research 
Specialist II to be part of Cedars-Sinai's commitment to Precision Health 
through an exciting opportunity within our IBD Drug Discovery and Development 
Unit (IBD3). We are a multidisciplinary basic, translational and clinical 
program devoted to mucosal inflammation. The mission of the IBD3 unit is to use 
personalized medicine approaches to predict the success of current and future 
therapeutic for inflammatory bowel diseases. The IBD3 program is u uniquely 
structured to join academic science with industry partners to discover and 
validate new therapeutic targets, accelerate drug development through patient 
stratification, and rescue and repurpose failed drugs by identifying drug 
responsive patient populations. The unit embodies a spirit of discovery with 
world leaders and research scientists on the care and management of IBD.



More information can be found at: 
https://www.cedars-sinai.edu/Research/Research-Labs/Bilsborough-Lab/



The IBD3 unit is seeking a mission-focused Research Specialist II, with the 
expertise in the development of protein expression and purification strategies 
to support ongoing drug discovery and development needs. Under the leadership 
of the IBD3 unit Director, the Research Specialist II will utilize a solid 
foundation in research and experience with techniques associated with a 
specific area of research.  Incumbent will be capable of exercising independent 
judgment while developing and implementing research programs, project planning, 
enrollment of patients, experimental protocols and procedures, database 
development and analysis including evaluating and interpreting results.  Will 
supervise lab activities, including research grant management, human resources, 
responsibility delegation, and provide training to other individuals who may be 
assigned to the project, study, or laboratory.  Reports to and works closely 
with Principal Investigator and has independent supervision of a laboratory or 
program.  Will prepare grant proposals, publications, and presentations. Will 
function as a bridge between research and clinical programs which may have 
local and national contributors and investigators relying on information 
provided.  Will have delegated authority to make substantive decisions and 
commitments in accord with the established goals and objectives of the 
laboratory or program.



Essential Job Duties and Responsibilities:



- Acts as a project lead and coordinator interacting with collaborators, 
clinical research personnel and researchers as part of a research team.

- Participates in all aspects of clinical development and study management 
(protocol design, enrollment of patients, development and implementation of 
protocols, and if applicable, submission of IRB applications and approvals).

- Follows established procedures or protocols to perform laboratory tests 
and/or experiments which will include: basic tissue culture, immunoassays, 
molecular biology techniques, microscopy, animal preparation (e.g. tail vein 
injections) and surgery.

- Provides scientific expertise to ongoing and future trials.

Identify and resolve common problems involved in routine research assays.

- Establishes and maintains relationships with clinical investigators and 
manages internal and external collaborative research projects.

- Acts as a scientific resource for the affiliated pre-clinical research 
laboratory (e.g., assisted with experimental designs, data analysis, 
interpretation of scientific literature).

- Supervises, leads, and trains other individuals assigned to the lab.

- Prepares grant applications and oversees submission process, including 
writing of grant proposal.

- Capable of exercising independent judgment while participating in the 
planning of experiments and evaluating and interpreting results.

- Operates appropriate laboratory equipment.

- Monitors inventory levels, orders materials and supplies in accordance with 
established policies and procedures.

- Operates lab computers for data entry and maintains accurate data records.

- Uses various software applications, such as spreadsheets, electronic mail, 
World Wide Web, statistical packages, and graphics packages to assemble, 
manipulate and/or format data and/or test reports.



Department and/or Unit Specific:



- Must demonstrate strong biochemistry skills and keeps up-to-date with the 
latest technologies to continually improve operational procedures.

- Able to Implement a variety of expression systems including e.coli, mammalian 
and baculovirus cell culture

- Hands on expertise in construct design, protein expression and purification

- Proven experience in difficult-to-express and purify proteins such as 
membrane proteins, enzymes and Fc-fusion for biologics, X-ray crystallography 
and    cryo-EM

- Works closely with computational scientists for structure-function studies 
and structure based drug design

- Uses protein biochemistry and structural biology knowledge to outline 
strategies and workflows for optimization of protein production needs

- Supports assay development in line with the needs of projects within the drug 
development group

- Supervise and train laboratory staff in assay development and protein 
expression and production technologies as needed.

- Manages collaborations with CRO’s for protein production, structure 
determination and manufacturing of proteins and protein therapeutics to ensure 
timelines, budgets and project goals are met.

- Communicates with other groups within Cedars-Sinai to facilitate a 
collaborative environment for the optimization of data analysis and to 
facilitate drug discovery and development efforts.

- Maintains strict adherence to research compliance regulatory standards for 
human and animal subject use.

- Ensures compliance with state and federal laws, accreditation, professional 
and regulatory agency standards including quality assurance and licensure 
requirements within the divisions. Assist in establishing and maintaining a 
quality assurance program acceptable to CSMC as required by The Joint 
Commission, state and other agencies, which shall include a systematic review 
of the quality, safety, and appropriateness of services rendered.

- Works to ensure internal budgets and goals are met and generates reports and 
presentations to ensure appropriate communication of findings.



Educational Requirements:

BS/BA, or equivalent, in biological sciences, chemistry, or related discipline 
required.  MS or PhD preferred.



Experience:

Five to seven (5-7) years of experience in area of research specialty and with 
post-undergraduate experience in a comparable laboratory performing relevant 
techniques.  Training and knowledge in the design and conduct of clinical 
trials.  Expertise in translational biomedical research. Knowledge of 
biostatistics as it is applied to clinical trial data analysis. Ability to 
communicate scientific and clinical information in the context of 
multidisciplinary teams.  Must demonstrate excellent communication skills, 
written and verbal. Strong computer skills are essential.



- PhD or highest degree in their field, preferred.

- Demonstrated significant, original, and creative contributions to a research 
or creative program or project.

- Completion of postdoctoral appointment in area of specialization.

- Minimum of 3 years as a postdoctoral fellow. Completion of postdoctoral 
appointment in area of specialization.

- Knowledge of PI’s area of research specialization. Demonstrated technical 
competency in a variety of research techniques and protocols.





Attention Applicants:



If you are the right candidate for this position, please e-mail address below, 
include cover letter with your research interests and career aims, CV (please 
include technology and skills proficient in) and contact information for three 
references.



Janine Bilsborough, PhD

Director, Inflammatory Bowel Disease Drug Discovery & Development

Email:   janine.bilsboro...@cshs.org






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