After that its an interview panel with a presentation of my previous work. 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 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. Conference Call to Discuss Third Quarter 2022 Results. Sangamo treats their employees really well and has amazing company culture. Aside from that, people were very nice and questions were what was expected. HR screen is just going over the Job Description and why Sangamo. Background and experience. Our ability to fund our projects enables us to execute and deliver on our mission. The process took 3 days. There can be no assurance that we and our collaborators will be able to develop commercially viable products. 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. 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. Four patients were withdrawn from enzyme replacement therapy (ERT) and maintained significantly elevated levels of -Gal A activity up to 28 weeks post withdrawal. Overall, 89% of employees would recommend working at Sangamo Therapeutics to a friend. Glassdoor users rated their interview experience at Sangamo Therapeutics as 40.0% positive with a difficulty rating score of 2.86 out of 5 (where 5 is the highest level of difficulty). I applied online. Coworkers are all very helpful and friendly. 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. Since the cutoff date, the fifth and final patient in the dose escalation phase who started the study on ERT has been withdrawn from ERT. Copyright 2008-2023, Glassdoor, Inc. "Glassdoor" and logo are registered trademarks of Glassdoor, Inc. Super friendly working environment and very nice people. 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. BRISBANE, Calif., February 22, 2023--SANGAMO THERAPEUTICS REPORTS RECENT BUSINESS HIGHLIGHTS AND FOURTH QUARTER AND FULL YEAR 2022 FINANCIAL RESULTS, BRISBANE, Calif., February 22, 2023--Sangamo Therapeutics Announces Evidence of Clinical Benefit in Phase 1/2 STAAR Study in Fabry Disease. media@sangamo.com, Sangamo Therapeutics Reports Recent Business Highlights and Second Quarter 2022 Financial Results, https://www.businesswire.com/news/home/20220804005384/en/, (unaudited; in thousands, except per share data), 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. The conference call dial-in numbers are (877) 377-7553 for domestic callers and (678) 894-3968 for international callers. Interview difficulty. Unorganized at best. Why Sangamo? All patients withdrawn have remained off ERT. As of the November 15, 2022, supplemental cutoff date, 13 patients exhibited supraphysiological levels of -Gal A activity, sustained for over two years for the patient with the longest follow-up. A pivotal data readout is estimated in late 2023 or early 2024. We expect our non-GAAP total operating expenses, excluding estimated non-cash stock-based compensation expenses of approximately $35 million, to be in the range of approximately $280 million to $290 million. A change of -17% or more over 10 trading days is a 9% . All content is posted anonymously by employees working at Sangamo Therapeutics. 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. Based on 2 interviews. Tell me about yourself? Sangamo Therapeutics, Inc. Careers Website www.sangamo.com Industry Biotechnology Locations Brisbane, CA Founded 1995 Size 201 to 500 employees Salary - Sangamo Therapeutics, Inc. 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. This is the Sangamo Therapeutics company profile. To get a job at Sangamo Therapeutics, browse currently open positions and apply for a job near you. Sangamo Therapeutics Inc (NASDAQ: SGMO) announced updated preliminary data as of October 20, 2022, the cutoff date from the Phase 1/2 STAAR study of isaralgagene civaparvovec, or ST-920, a wholly. Sangamo Therapeutics Reports Recent Business Highlights and Third Quarter 2022 Financial Results News Release Sangamo Therapeutics Announces Updated Preliminary Phase 1/2 Data in Fabry Disease Showing Continued Tolerability and Sustained Elevated -Gal A Enzyme Activity in Nine Patients News Release Consolidated net loss for the third quarter ended September 30, 2022 was $53.2 million, or $0.34 per share, compared to a net loss of $47.7 million, or $0.33 per share, for the same period in 2021. 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. Our platforms have yielded multiple clinical stage programs that could provide value in the near-to-mid-term. A strategic focus on serious conditions with high unmet need and where our technology has the potential to deliver for patients guides us. Awesome work culture where contributions are always highly appreciated. Duties of the advertised position and the involved project. 24/7 Wall St. Staff. Glassdoor has 55 Sangamo Therapeutics reviews submitted anonymously by Sangamo Therapeutics employees. HR screen is just going over the Job Description and why Sangamo. For Sangamo Therapeutics, science is a means to develop new medicines with the potential to transform the lives of patients living with serious genetic diseases. Fabry disease Reported data updates from the Phase 1/2 STAAR studys dose escalation phase; Dose expansion phase underway and dosing commenced; Phase 3 planning progresses. I interviewed at Sangamo Therapeutics. Sickle cell disease Dosed sixth patient, the second with a product candidate manufactured using improved methods; Phase 3 planning progresses. 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. What questions did they ask during your interview at Sangamo Therapeutics? Company seemed to have an outdated and rigid mindset. Sangamo was founded in 1995 as Sangamo BioSciences, Inc. in order to research new technologies for genome editing. How is diversity at Sangamo Therapeutics? General high turnover rate in biotech industry applies here as well. About a day or two. Sangamo Therapeutics is a genomic medicine company focused on leveraging our novel platforms and scientific expertise to advance clinical programs. 89% of employees would recommend working at, According to anonymously submitted Glassdoor reviews, Sangamo Therapeutics employees rate their compensation and benefits as 4.0 out of 5. These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. I interviewed at Sangamo Therapeutics (Richmond, CA) in Jul 2019. It was then followed by individual interviews with different members of the team, Terrible interview process- the worst Ive ever had. Be the first to find this interview helpful. The product candidate continues to be generally well tolerated in both patients. Guided by Science. Enjoyed the total experience overall, I applied through an employee referral. There is a unified sense of purpose. Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicines company, today reported recent business highlights and third quarter 2022 financial results. While not required, it is recommended you join 10 minutes prior to the event start. Analyst Report: Alnylam Pharmaceuticals, Inc. Analyst Report: BioMarin Pharmaceutical Inc. NasdaqGS - NasdaqGS Real Time Price. 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. No post about Sangamo Therapeutics, Inc. yet, Hemophilia Market to Showcase Robust Growth in the Upcoming Year to 2032 | MobileODT, Gals Bio Ltd, DiagnoseSt, Global mRNA Vaccine Market Size And Forecast | Argos Therapeutics BioNTech AG, CureVac AG, eTheRNA Immunotherapies, Ethris GmbH, Incellart, Moderna Sangamo Therapeutics Tiba Biotech, Translate Bio, Inc. Sioux City Catholic Globe, We don't have enough salaries for I interviewed at Sangamo Therapeutics (San Francisco, CA) in Aug 2020. 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. BRISBANE, Calif.--(BUSINESS WIRE)--Aug. 4, 2022-- 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. Do the numbers hold clues to what lies ahead for the stock? Three weeks. I am able to speak with VPs of many different departments with ease. Good, great, fine, virtual, lovely. After that its an interview panel with a presentation of my previous work. Sangamo Therapeutics is a genomic medicine company focused on leveraging our novel platforms and scientific expertise to advance clinical programs. We expect to present additional clinical updates from the STAAR study, including the first data from the expansion cohort, in the first half of 2023. Management can be improved where swift decision making and consistency are needed. We continue to expect non-GAAP total operating expenses, excluding estimated non-cash stock-based compensation expense of approximately $40 million, in the range of approximately $280 million to $310 million in 2022. 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. Due to the split at Richmond and Brisbane, there was confusion on which site to interview. Glassdoor has millions of jobs plus salary information, company reviews, and interview questions from people on the inside making it easy to find a job thats right for you. Our goal is to develop a wholly owned genomic medicine portfolio, which we fund via our collaborations with blue-chip biopharmaceutical partners, which have already brought in $815M in upfronts and milestones with billions in potential milestone payments. I applied through college or university. The process took 3 days. Interview experience. Reviews 5.0 1 reviews 5.0 Career Growth 5.0 Work - Life Balance 4.0 Compensation / Benefits 5.0 Company Culture 4.0 Management POPULAR 4.0 "Great overall biotech company" Get started with your Free Employer Profile. Share your interview experience. 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. Winning Companies champion board diversity by having 20% or more of their board seats held by women. Sangamo Therapeutics employees rate the overall compensation and benefits package 4.0/5 stars. Good overall compensation and benefits. Fantastic, Participants should register for, and access, the call using this link. 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. Renal Transplant Rejection Received Orphan Medicinal Product Designation from the European Commission; progressed manufacturing and clinical activities ahead of anticipated Q3 dosing. View all news about Sangamo Therapeutics, Inc. 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. This is the second patient in the study to receive a product candidate manufactured using improved methods that have been shown in internal experiments to increase the number of long-term progenitor cells in the final product. However, after the last interview I haven't heard back from them. Sangamo Therapeutics saw global potential for TxCell's lead candidate TX200 as the anchor of a pipeline of chimeric antigen receptor . This is based on 44 anonymously submitted reviews on Glassdoor. 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. My three times follow-up with two different HR reps was left unanswered. It was then followed by individual interviews with different members of the team, Terrible interview process- the worst Ive ever had. The decrease in total operating expenses on a GAAP basis was primarily due to the timing of certain research and development activities. When did GD start to be awful? A replay will be available following the conference call, accessible under Events and Presentations. Barclays Gene Editing & Gene Therapy Summit. Find a Great First Job to Jumpstart Your Career, Getting a Job Is Tough; This Guide Makes it Easier, Climb the Ladder With These Proven Promotion Tips, A Guide to Negotiating the Salary You Deserve. While not required, it is recommended you join 10 minutes prior to the event start. I interviewed at Sangamo Therapeutics (New York, NY). Over 50% of the patients have been enrolled in the Phase 3 AFFINE trial. The average Sangamo Therapeutics salary ranges from approximately $88,067 per year for a Research Associate II to $240,483 per year for an Associate Director. 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. Phase 3 study design, enabling activities and manufacturing readiness are in progress. Pros & Cons are excerpts from user reviews. I interviewed at Sangamo Therapeutics in Jan 2021. I interviewed at Sangamo Therapeutics (San Francisco, CA) in Aug 2020. Why Sangamo? These increases were partially offset by a decrease of $0.7 million in revenue related to our collaboration agreement with Biogen. 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. We expect to present updated data from the Phase 1/2 ALTA study via a poster presentation at the ASH Annual Meeting in December. Enzyme replacement therapy (ERT) withdrawal was completed for an additional two patients previously dosed in the STAAR study, achieving a total of four patients to date who have successfully been withdrawn. Cash, cash equivalents and marketable securities. Based on 2 interviews. The hiring process at Sangamo Therapeutics takes an average of 31 days when considering 17 user submitted interviews across all job titles. (This interview has been lightly edited for length and . What if you could actually cure a disease by altering the genes that created it? Employees also rated Sangamo Therapeutics 4.1 out of 5 for work life balance, 4.5 for culture and values and 3.8 for career opportunities. Gene editing is a very compelling concept for physicians. What are perks and other benefits like at Sangamo Therapeutics? There can be no assurance that we and our collaborators will be able to develop commercially viable products. Filler, words, noun, verb, et cetera. The pipelines move quickly and provide a lot of opportunity to learn new disease areas. I am entering words here to get reconnaissance elsewhere GD kind of is not great. It was well thought out and carried out professionally. How many more words to count? 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. Do shift work. 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. BRISBANE, Calif.--(BUSINESS WIRE)--Nov. 3, 2022-- I wasn't happy with the unprofessional manner. Financial Guidance for 2022 Reiterated (initial guidance provided on February 24, 2022). The call will also be webcast with live Q&A and can be accessed via a link on the Sangamo Therapeutics website in the Investors and Media section under Events and Presentations. Questions asked were appropriate and aimed at confirming the candidate possesses the required skills and would be a good fit into the company. This press release features multimedia. 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. How do employees rate the business outlook for Sangamo Therapeutics? Received Regenerative Medicine Advanced Therapy (RMAT) designation from the FDA for BIVV003. Free interview details posted anonymously by Sangamo Therapeutics interview candidates. Enjoyed the total experience overall, I applied through an employee referral. The process took 3 months. These improved manufacturing methods have been shown in internal experiments to increase the number of long-term progenitor cells in the final product. Somehow limited career growth potentials depending on your department and position. Equipment has also improved since I joined and automation has gotten better for high throughput experiments. 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. Changes wont be saved until you sign up for an Enhanced Profile subscription. Results Oriented. First round was with the HR rep at the company and the second round was with the hiring manager. Pfizer and Sangamo announced that recruitment has re-opened 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. Sickle cell disease Completed transition of program back to Sangamo; advanced manufacturing activities in anticipation of dosing in Q3; Phase 3 planning progresses. How many more words to count? Duties of the advertised position and the involved project. This report was sent to Briefing.com subscribers earlier today. We have a robust preclinical pipeline with programs in emerging areas that could provide value in the mid-to-long term. A pivotal readout is expected in the first half of 2024. Difficult. To learn more, visit www.sangamo.com and connect with us on LinkedIn and Twitter. Conference Call to Discuss Second Quarter 2022 Results. Management is very accessible. Background and experience. 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. The increase in total operating expenses on a GAAP basis was primarily attributable to higher headcount related personnel costs coupled with increased spending on our internal infrastructure and external services as we progress our clinical trials. 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