Recruiter set up the interview. Questions asked were appropriate and aimed at confirming the candidate possesses the required skills and would be a good fit into the company. While not required, it is recommended you join 10 minutes prior to the event start. Guided by Science. Sangamo is a genomic medicine company that seeks to help millions of people who suffer from severe diseases for which todays medicine can only offer symptom management at best. Our platforms have yielded multiple clinical stage programs that could provide value in the near-to-mid-term. The Sangamo management team will discuss these results on a conference call today, Thursday November 3, 2022, at 4:30 p.m. Eastern Time. Find your private company bowl on Fishbowl, join the hottest conversation with your colleagues anonymously. Participants should register for, and access, the call using this link. Changes wont be saved until you sign up for an Enhanced Profile subscription. The decrease in total operating expenses on a GAAP basis was primarily due to the timing of certain research and development activities. 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. Dosed the second patient in the Phase 1/2 STEADFAST study evaluating TX200, our wholly owned autologous CAR-Treg cell therapy treating patients receiving an HLA-A2 mismatched kidney from a living donor. Non-GAAP operating expenses, which exclude stock-based compensation expense, for the second quarter ended June 30, 2022, were $67.2 million, compared to $67.1 million for the same period in 2021. Financial Guidance for 2022 Narrowed (initial guidance provided on February 24, 2022). Subscribe to Yahoo Finance Plus to view Fair Value for SGMO. How do employees rate the business outlook for Sangamo Therapeutics? The process took 3 months. Having problems? Our platforms have yielded multiple clinical stage programs that could provide value in the near-to-mid-term. Total operating expenses on a GAAP basis for the third quarter ended September 30, 2022 were $81.3 million, compared to $77.0 million for the same period in 2021. 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. A pivotal readout is expected in the first half of 2024. Currency in USD, Gain actionable insight from technical analysis on financial instruments, to help optimize your trading strategies. 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. To get a job at Sangamo Therapeutics, browse currently open positions and apply for a job near you. 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. Questions asked were appropriate and aimed at confirming the candidate possesses the required skills and would be a good fit into the company. Do shift work. The process took 4 weeks. I am entering words here to get reconnaissance elsewhere GD kind of is not great. Results Oriented. The link to access the live webcast can also be found on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. ProsGreat science and robust pipelines. I applied through an employee referral. This non-GAAP financial measure is in addition to, not a substitute for, or superior to, measures of financial performance prepared in accordance with GAAP. Salary expectation. "This has been a year marked by progress across our pipeline. 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 projects at Sangamo are top notch and collaborations are in place with industry leaders. Participants should register for, and access, the call using this link. Sangamo plans to participate in the following events in the fourth quarter: Access links for available webcasts for these investor conferences will be available on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. Will Gene Editing Be in Your Medical Future? I interviewed at Sangamo Therapeutics in Aug 2020, Nice set of interviews and great questions. I interviewed at Sangamo Therapeutics in Jan 2021. Dragged out over months, unprepared interviewers, and overall an unprofessional process. These increases were partially offset by a decrease of $0.7 million in revenue related to our collaboration agreement with Biogen. Why Sangamo? Copyright 2008-2023, Glassdoor, Inc. "Glassdoor" and logo are registered trademarks of Glassdoor, Inc. Brisbane, California, November 16, 2022 Dosing has resumed in the Phase 3 AFFINE study evaluating giroctocogene fitelparvovec, an investigational gene therapy for patients with moderately severe to severe hemophilia A. Dosing resumed on November 10, 2022. Presented seven posters and one oral presentation at ASGCT on. Technical assay related questions? We are passionate about our science and driven by the purpose it serves. Management is very accessible. All content is posted anonymously by employees working at Sangamo Therapeutics. Trial sites will begin to resume enrollment this month . These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. Sangamo Therapeutics Announces Updated Preliminary Phase 1/2 Data in Fabry Disease Clinical Study Showing Continued Tolerability and Sustained Elevated -gal A Enzyme Activity in Five Longest Treated Patients | Sangamo Therapeutics, Inc. These forward-looking statements include, without limitation, statements relating to: the therapeutic and commercial potential of our product candidates and their ability to generate value for our shareholders, the anticipated plans and timelines of Sangamo and our collaborators for screening, enrolling and dosing patients in and conducting our ongoing and potential future clinical trials and presenting clinical data from our clinical trials, including plans to dose patients in the expansion phase of, and the presentation of updated clinical data from, the Phase 1/2 STAAR study and updates regarding the PRECIZN-1 study, the dosing of patients with product candidates using improved manufacturing methods in the PRECIZN-1 study and the potential impacts thereof, as well as the timing and expectations for completion of dosing in such study, the expected timeline for dosing additional patients in the STEADFAST study, the anticipated advancement of our product candidates to late-stage development including potential future Phase 3 trials, plans and timing regarding the expected resumption of dosing of patients in the Phase 3 AFFINE trial and the presentation of data from such trial, our 2022 financial guidance related to GAAP and non-GAAP total operating expenses and stock-based compensation, and other statements that are not historical fact. Good, great, fine, virtual, lovely. Copyright 20082023, Glassdoor, Inc. "Glassdoor" and logo are registered trademarks of Glassdoor, Inc. Sangamo BioSciences, Inc. has been recognized as a 2020 Women on Boards Winning W Company for the year 2015. Cash, cash equivalents and marketable securities as of June 30, 2022, were $363.7 million, compared to $464.7 million as of December 31, 2021. Our ability to fund our projects enables us to execute and deliver on our mission. Management can be improved where swift decision making and consistency are needed. Available materials will be found on the Sangamo Therapeutics website after the event. Consolidated net loss for the second quarter ended June 30, 2022, was $43.2 million, or $0.29 per share, compared to a net loss of $47.2 million, or $0.33 per share, for the same period in 2021. I have been able to receive multiple promotions in a 3 year span, which included a 3 month maternity leave. Filler, words, noun, verb, et cetera. Salary expectation. 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. Tell me a little about your self. I applied through college or university. Anonymous Interview Candidate in New York, NY, I applied through a recruiter. Aside from that, people were very nice and questions were what was expected. Filler, words, noun, verb, et cetera. 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. Phase 3 enabling activities and manufacturing readiness are in progress. I interviewed at Sangamo Therapeutics in Jan 2021. These increases were partially offset by reimbursement of certain research and development expenses by Sanofi under the termination agreement. Sangamo plans to participate in the following events in the third quarter: Access links for these investor conferences will be available on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. BRISBANE, Calif.--(BUSINESS WIRE)--Aug. 4, 2022-- Over 50% of the patients have been enrolled in the Phase 3 AFFINE trial. May 26, 2020. Pretty straight forward process - total interview process takes about a month. I interviewed at Sangamo Therapeutics (New York, NY). We continue to actively prepare for a potential pivotal Phase 3 trial. Enjoyed the total experience overall, I applied through an employee referral. Sickle cell disease Dosed sixth patient, the second with a product candidate manufactured using improved methods; Phase 3 planning progresses. https://www.openpr.com/news/2771399/hemophilia-market-to-showcase-robust-growth-in-the-upcoming-year, https://www.catholicglobe.org/global-mrna-vaccine-market-insight-size-and-forecast/. ET to review its fourth quarter and full year 2022. We made meaningful progress advancing our clinical-stage programs in the second quarter, said Sandy Macrae, Chief Executive Officer of Sangamo. They said they get tested for Sars once a week, which is great too. We encourage investors to carefully consider our results under GAAP, as well as our supplemental non-GAAP financial information, to more fully understand our business. We dosed the sixth patient in the Phase 1/2 PRECIZN-1 study of BIVV003, a zinc finger nuclease gene-edited cell therapy candidate for the treatment of sickle cell disease. Each step toward the possibility of eliminating the need for frequent, life-long treatment for the patients and families affected by debilitating disease is exciting. Since we dosed the first patient in the Phase 1/2 STEADFAST study evaluating TX200, our wholly owned autologous CAR-Treg cell therapy treating patients receiving an HLA-A2 mismatched kidney from a living donor, the product candidate continues to be generally well tolerated, with no treatment related adverse events. We expect to dose two additional patients imminently, and have multiple patients in screening, including both male and female candidates. The increase of $1.5 million in revenues was primarily attributed to an increase of $1.3 million in revenue related to our collaboration agreement with Novartis and an increase of $0.8 million in revenue related to our collaboration agreement with Sanofi. Sangamo was founded in 1995 as Sangamo BioSciences, Inc. in order to research new technologies for genome editing. Renal Transplant Rejection Received Orphan Medicinal Product Designation from the European Commission; progressed manufacturing and clinical activities ahead of anticipated Q3 dosing. Pfizer advised us that it continues to anticipate resuming the dosing of additional patients in the Phase 3 AFFINE trial of giroctocogene fitelparvovec, an investigational gene therapy we are developing with Pfizer for patients with moderately severe to severe hemophilia A, in the third quarter of 2022. Conference Call and Webcast Scheduled for 4:30 p.m. Eastern Time. To supplement our financial results and guidance presented in accordance with GAAP, we present non-GAAP total operating expenses, which exclude stock-based compensation expense from GAAP total operating expenses. Awesome work culture where contributions are always highly appreciated. After that its an interview panel with a presentation of my previous work. - Achieved 78% globotriaosylceramide (Gb3) substrate clearance at 6-months and 77% reduction in urine podocyte loss in one of, BRISBANE, Calif. --(BUSINESS WIRE)--Feb. 21, 2023-- Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicine company, announced today that the company is scheduled to hold a conference call on Wednesday, February 22, 2023 at 4:30 p.m. Difficult. There can be no assurance that we and our collaborators will be able to develop commercially viable products. Based on 2 interviews. These risks and uncertainties are described more fully in our Securities and Exchange Commission filings and reports, including in our Annual Report on Form 10-K for the year ended December 31, 2021, as supplemented by our Quarterly Report on Form 10-Q for the quarter ended September 30, 2022. Sangamo Therapeutics employees rate the overall compensation and benefits package 4.0/5 stars. Cash, cash equivalents and marketable securities as of September 30, 2022, were $350.3 million, compared to $464.7 million as of December 31, 2021. Conference Call to Discuss Third Quarter 2022 Results. Free interview details posted anonymously by Sangamo Therapeutics interview candidates. Gene editing is a very compelling concept for physicians. February 27, 2023 9:47 am. Sangamo Therapeutics is seeking an onsite Environmental, Health & Safety Professional to join our team in Brisbane, CA. Sangamo Therapeutics is a genomic medicine company focused on leveraging our novel platforms and scientific expertise to advance clinical programs. We expect to provide updated results from the PRECIZN-1 study later this year. Technical assay related questions? Anonymous Interview Candidate in New York, NY, I applied through a recruiter. 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. Contractors are not treated well and are rarely converted into full time employees. 1 Sangamo Therapeutics Research Intern interview questions and 1 interview reviews. I interviewed at Sangamo Therapeutics. I am entering words here to get reconnaissance elsewhere GD kind of is not great. Actual results may differ materially from those projected in these forward-looking statements due to the risks and uncertainties described above and other risks and uncertainties that exist in the operations and business environments of Sangamo and our collaborators. We have excluded stock-based compensation expense because it is a non-cash expense that may vary significantly from period to period as a result of changes not directly or immediately related to the operational performance for the periods presented. 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. - 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. 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. 38% of job seekers rate their interview experience at Sangamo Therapeutics as positive. I interviewed at Sangamo Therapeutics. We're pioneering the future of genomic medicine Company seemed to have an outdated and rigid mindset. Would never interview here again, HR screen, Manager, Team. 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. Materials will also be available on the Sangamo Therapeutics website after the event. This employer has claimed their Employer Profile and is engaged in the Glassdoor community. Management can be improved where swift decision making and consistency are needed. We were proud to present promising updated preliminary data from our wholly owned Fabry study, to resume our partnered Hemophilia A pivotal trial, and to continue dosing in our renal transplant rejection and sickle cell studies. Based on 2 interviews. However, after the last interview I haven't heard back from them. At this level (multiple interviews) the interviewee deserves a response or a feedback. Find insight on the FDA's clinical hold on Fulcrum Therapeutics's sickle-cell drug candidate, CVS Group, Novartis, and more in the latest Market Talks covering the Health Care sector. We believe that manufacturing is a strategic advantage and gives us greater control over timelines, quality and supply. The interview was timely, provided an overview of the company and of the role, asked the candidate to go over their relevant career trajectory and competences. The conference call dial-in numbers are (877) 377-7553 for domestic callers and (678) 894-3968 for international callers. I wasn't happy with the unprofessional manner. These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. 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. Super friendly working environment and very nice people. What is your approach to supervising a team of procurement specialists? Our rare disease clinical programs are feeding insights across our portfolio and paving the way for research and preclinical programs across larger patient populations. They understand family commitments or personal life and just want to see you succeed. 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. 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