We're pioneering the future of genomic medicine When did GD start to be awful? I think it depends what you prioritize in a workplace, benefits, etc. Salary expectation. Pays significantly less than South San Francisco companies. Interview experience. Get started with your Free Employer Profile. In the third quarter, we continued to advance our clinical trials and preclinical activities while maintaining fiscal discipline and operational excellence, said Sandy Macrae, Chief Executive Officer of Sangamo. We expect to dose two additional patients imminently, and have multiple patients in screening, including both male and female candidates. Changes wont be saved until you sign up for an Enhanced Profile subscription. Super friendly working environment and very nice people. Available materials will be found on the Sangamo Therapeutics website after the event. This report was sent to Briefing.com subscribers earlier today. Candidates give an average difficulty score of 2.8 out of 5 (where 5 is the highest level of difficulty) for their job interview at Sangamo Therapeutics. There can be no assurance that we and our collaborators will be able to develop commercially viable products. Louise Wilkieir@sangamo.com All answers shown come directly from Sangamo Therapeutics Reviews and are not edited or altered. We believe that this non-GAAP financial measure, when considered together with our financial information prepared in accordance with GAAP, can enhance investors and analysts ability to meaningfully compare our results from period to period and to our forward-looking guidance, and to identify operating trends in our business. Copyright 2008-2023, Glassdoor, Inc. "Glassdoor" and logo are registered trademarks of Glassdoor, Inc. We are engaging in pivotal study-enabling activities in two of our clinical stage programs and are preparing to complete dosing of the first cohort in our TX200 program, which recently received Orphan Medicinal Product Designation from the European Commission. Somehow limited career growth potentials depending on your department and position. Sangamo Therapeutics is a clinical-stage biopharmaceutical company with a robust genomic medicines pipeline. Factors that could cause actual results to differ include, but are not limited to, risks and uncertainties related to the effects of the evolving COVID-19 pandemic and the impacts of the pandemic and other macroeconomic factors, including as a result of the ongoing conflict between Russia and Ukraine, on the global business environment, healthcare systems and business and operations of Sangamo and our collaborators, including the initiation and operation of clinical trials; the research and development process, including the enrollment, operation and results of clinical trials and the presentation of clinical data; the uncertain timing and unpredictable nature of clinical trial results, including the risk that therapeutic effects in the Phase 3 AFFINE trial will not be durable in patients as well as the risk that the therapeutic effects observed in the latest preliminary clinical data from the Phase 1/2 STAAR study and the Phase 1/2 PRECIZN-1 study will not be durable in patients and that final clinical trial data from the study will not validate the safety and efficacy of isaralgagene civaparvovec, or BIVV003 (formerly known as SAR44513); the unpredictable regulatory approval process for product candidates across multiple regulatory authorities, including the potential that health authorities will not issue the required protocol amendment approvals in the Phase 3 AFFINE trial in a timely manner, or at all; reliance on results of early clinical trials, which results are not necessarily predictive of future clinical trial results, including the results of any Phase 3 trial of our product candidates; our limited experience manufacturing biopharmaceutical products, including the risks that we may be unable to maintain compliant manufacturing facilities, build additional facilities and manufacture our product candidates as intended; the potential for technological developments that obviate technologies used by Sangamo; the potential that Sangamo will not be able to identify and secure options or new collaborators for the BIVV003 program; the potential for Sangamo to cease development of the BIVV003 program, whether due to its inability to secure options to advance the program or otherwise;our lack of resources to fully develop, obtain regulatory approval for and commercialize our product candidates; and our ability to achieve expected future financial performance. Questions asked were appropriate and aimed at confirming the candidate possesses the required skills and would be a good fit into the company. Our platforms have yielded multiple clinical stage programs that could provide value in the near-to-mid-term. I interviewed at Sangamo Therapeutics (New York, NY). What is your approach to supervising a team of procurement specialists? Forward-looking statements contained in this announcement are made as of this date, and we undertake no duty to update such information except as required under applicable law. Really collaborative environment Great coworkers Very supportive community, Promotions based on seniority rather than merit HR does not really help solve problems, Great people, good environment, interesting science. Super friendly working environment and very nice people. We are passionate about our science and driven by the purpose it serves. Fair Value is the appropriate price for the shares of a company, based on its earnings and growth rate also interpreted as when P/E Ratio = Growth Rate. Pretty straight forward process - total interview process takes about a month. Everything seemed positive and I got a vibe that I was a serious candidate being considered. Using ground-breaking science, including our proprietary zinc finger genome engineering technology and manufacturing expertise, Sangamo aims to create new genomic medicines for patients suffering from diseases for which existing treatment options are inadequate or currently dont exist. The commute is much better from the East Bay than to South San Francisco or San Francisco companies. Sangamo Therapeutics saw global potential for TxCell's lead candidate TX200 as the anchor of a pipeline of chimeric antigen receptor . We plan to provide guidance on timing for dosing for the third patient once the kidney transplant has been scheduled. Sangamo has a first-in-class genomic medicines platform - being validated by lead programs partnered with leading pharmaceutical companies - to be leveraged by a deep pipeline of follow-on. Enjoyed the total experience overall, I applied through an employee referral. There is a unified sense of purpose. We expect to present updated data from the Phase 1/2 ALTA study via a poster presentation at the ASH Annual Meeting in December. These increases were partially offset by reimbursement of certain research and development expenses by Sanofi under the termination agreement. It was well thought out and carried out professionally. Our platforms have yielded multiple clinical stage programs that could provide value in the near-to-mid-term. Progressed clinical activities in preparation for the third patient. On a GAAP basis, we continue to expect total operating expenses in the range of approximately $320 million to $350 million in 2022, which includes non-cash stock-based compensation expense. I applied online. Difficult. The process took 3 months. How many more words to count? BRISBANE, Calif.--(BUSINESS WIRE)--Aug. 4, 2022-- - Sustained, elevated expression of alpha-galactosidase A (-Gal A) activity observed in 13 patients for over two years for the longest treated patient as of cutoff date. Non-GAAP operating expenses, which exclude stock-based compensation expense, for the third quarter ended September 30, 2022 were $73.5 million, compared to $69.1 million for the same period in 2021. The decrease of $2.1 million in revenues was primarily attributable to a decrease of $1.9 million and $1.6 million related to our collaboration agreements with Novartis and Biogen respectively, and a decrease of $1.1 million due to the termination of our collaboration agreement with Sanofi. Cash, cash equivalents and marketable securities. Interview difficulty. Over 50% of the patients have been enrolled in the Phase 3 AFFINE trial. Patient dosing is expected to resume in October New York, NY, and Brisbane, California, September 22, 2022 - Pfizer and Sangamo Therapeutics announced that the Phase 3 AFFINE study evaluating giroctocogene fitelparvovec, an investigational gene therapy for patients with moderately severe to severe hemophilia A, has re-opened recruitment. Due to the split at Richmond and Brisbane, there was confusion on which site to interview. As we look to next year and beyond, I am confident in Sangamos ability to carry out our mission of developing transformational therapies for patients in need.. This rating has been stable over the past 12 months. Technical assay related questions? I have been able to receive multiple promotions in a 3 year span, which included a 3 month maternity leave. Presented seven posters and one oral presentation at ASGCT on. Sangamo uses its deep scientific expertise and proprietary zinc finger technology to create genomic cures for patients suffering from severe diseases for which todays medicine can only offer symptom management at best. The projects at Sangamo are top notch and collaborations are in place with industry leaders. Revenues for the second quarter ended June 30, 2022, were $29.4 million, compared to $27.9 million for the same period in 2021. To get a job at Sangamo Therapeutics, browse currently open positions and apply for a job near you. Pfizer Inc. (NYSE: PFE) and Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicines company, today announced that the first participant has been dosed in the Phase 3 AFFINE study of giroctocogene fitelparvovec (SB-525), an investigational gene therapy for hemophilia A patients. Once registered, participants will be given the option to either dial into the call with the number and unique passcode provided or to use the dial-out option to connect their phone instantly. Common stages of the interview process at Sangamo Therapeutics according to 17 Glassdoor interviews include: Find a Great First Job to Jumpstart Your Career, Stand Out From the Crowd With the Perfect Cover Letter, How to Prepare for Your Interview and Land the Job. Factors that could cause actual results to differ include, but are not limited to, risks and uncertainties related to the effects of the evolving COVID-19 pandemic and the impacts of the pandemic and other macroeconomic factors, including as a result of the ongoing conflict between Russia and Ukraine, on the global business environment, healthcare systems and business and operations of Sangamo and our collaborators, including the initiation and operation of clinical trials; the research and development process, including the enrollment, operation and results of clinical trials and the presentation of clinical data; the impacts of clinical trial delays, pauses and holds on clinical trial timelines and commercialization of product candidates, including the risk that any necessary conditions to resume dosing of patients in the Phase 3 AFFINE trial are not met in a timely manner, or at all;the uncertain timing and unpredictable nature of clinical trial results, including the risk that therapeutic effects in the Phase 3 AFFINE trial will not be durable in patients as well as the risk that the therapeutic effects observed in the latest preliminary clinical data from the Phase 1/2 STAAR study and the Phase 1/2 PRECIZN-1 study will not be durable in patients and that final clinical trial data from the study will not validate the safety and efficacy of isaralgagene civaparvovec or BIVV003, and that the patients withdrawn from ERT will remain off ERT; the unpredictable regulatory approval process for product candidates across multiple regulatory authorities; reliance on results of early clinical trials, which results are not necessarily predictive of future clinical trial results, including the results of any Phase 3 trial of our product candidates; our limited experience manufacturing biopharmaceutical products, including the risks that we may be unable to maintain compliant manufacturing facilities, build additional facilities and manufacture our product candidates as intended; the potential for technological developments that obviate technologies used by Sangamo; the potential for Sangamo to cease development of the BIVV003 program, whether due to its inability to secure options to advance the program or otherwise;our lack of resources to fully develop, obtain regulatory approval for and commercialize our product candidates; and our ability to achieve expected future financial performance. Interview process length. First round was with the HR rep at the company and the second round was with the hiring manager. These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. Due to the split at Richmond and Brisbane, there was confusion on which site to interview. ET to review its fourth quarter and full year 2022. I wasn't happy with the unprofessional manner. A pivotal data readout is estimated in late 2023 or early 2024. I applied through an employee referral. Coupled with strong advances in our preclinical pipeline, we believe this progress positions us well to advance the development of potentially transformational genomic medicines for patients in need and to generate long-term value for our shareholders.. We completed the transition of Sanofis rights and obligations under the collaboration developing BIVV003, formerly known as. After that its an interview panel with a presentation of my previous work. Our scientists are leaders in the. Point Richmond is a nice little downtown area as well. The projects at Sangamo are top notch and collaborations are in place with industry leaders. Revenues for the third quarter ended September 30, 2022 were $26.5 million, compared to $28.6 million for the same period in 2021. Our rare disease clinical programs are feeding insights across our portfolio and paving the way for research and preclinical programs across larger patient populations. Trial sites will begin to resume enrollment this month . Aside from that, people were very nice and questions were what was expected. Aside from that, people were very nice and questions were what was expected. Cash, cash equivalents and marketable securities. media@sangamo.com, Sangamo Therapeutics Reports Recent Business Highlights and Third Quarter 2022 Financial Results, https://www.businesswire.com/news/home/20221103005505/en/, Net loss attributable to non-controlling interest, Basic and diluted net loss per share attributable to, Shares used in computing basic and diluted net loss per share attributable to, Cash, cash equivalents, and marketable securities, Presented updated preliminary data from the Phase 1/2 STAAR study evaluating isaralgagene civaparvovec, our wholly owned gene therapy product candidate for the treatment of Fabry Disease at three separate conferences, most notably at the 29th. Do the numbers hold clues to what lies ahead for the stock? Tell me a little about your self. A change of -17% or more over 10 trading days is a 9% . Hemophilia A Announced, with Pfizer, the resumption of recruitment in the Phase 3 AFFINE trial; dosing is expected to resume shortly; pivotal data read-out expected in the first half of 2024. There are no open jobs at Sangamo Therapeutics, Inc. currently. Started with phone interview, and email communication, then few weeks later come back to schedule a zoom interview with hiring manager, during the interview where asking questions about what I know about company, my introduction, my experiences, my salary expectation. Company seemed to have an outdated and rigid mindset. Some details of my previous projects. 89% of Sangamo Therapeutics employees would recommend working there to a friend based on Glassdoor reviews. I interviewed at Sangamo Therapeutics (San Francisco, CA) in Aug 2020. Trial sites resumed enrollment in September, and dosing is expected to resume shortly. 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