The hiring process at Sangamo Therapeutics takes an average of 31 days when considering 17 user submitted interviews across all job titles. We plan to complete dosing of the first cohort, comprised of three patients, by the end of 2022. Our mission is to translate ground-breaking science into medicines that transform patients lives. It was then followed by individual interviews with different members of the team, To get a job at Sangamo Therapeutics, browse, Overall, 89% of employees would recommend, Work Here? - 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. I interviewed at Sangamo Therapeutics in Aug 2020, Nice set of interviews and great questions. Interview experience. 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. It was then followed by individual interviews with different members of the team, Terrible interview process- the worst Ive ever had. Do shift work. American Society of Gene and Cell Therapy (ASGCT) Profiled significant pre-clinical progress across Sangamos innovative pipeline and platform. Sangamo Therapeutics is a clinical-stage biopharmaceutical company with a robust genomic medicines pipeline. Progressed clinical activities in preparation for the third patient. Glassdoor users rated their interview experience at. Nothing striking about this particular process. 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. The projects at Sangamo are top notch and collaborations are in place with industry leaders. Preliminary data showed all nine patients from the dose escalation phase exhibited sustained elevated -Gal A activity, ranging from nearly 2-fold to 30-fold of mean normal, for up to 23 months post dosing, as of the last date of measurement. Phase 3 enabling activities and manufacturing readiness are in progress. 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. To learn more, visit www.sangamo.com and connect with us on LinkedIn and Twitter. Interview process length. Sangamo Therapeutics, Inc. (Nasdaq: SGMO), a genomic medicines company, today reported recent business highlights and second quarter 2022 financial results. Sangamo Therapeutics, Inc.(Nasdaq: SGMO), a genomic medicines company, today reported recent business highlights and second quarter 2022 financial results. Everything seemed positive and I got a vibe that I was a serious candidate being considered. However, I never hear back from them since then. 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. 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. Management is very accessible. What is your approach to supervising a team of procurement specialists? We continue to actively prepare for a potential pivotal Phase 3 trial. 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. Be the first to find this interview helpful. How many more words to count? Estimated return represents the projected annual return you might expect after purchasing shares in the company and holding them over the default time horizon of 5 years, based on the EPS growth rate that we have projected. Presented seven posters and one oral presentation at ASGCT on. Company is very dedicated to patient engagement as well as inclusion and diversity.Read More. HR screen is just going over the Job Description and why Sangamo. 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. See 1 answer. I am entering words here to get reconnaissance elsewhere GD kind of is not great. Will Gene Editing Be in Your Medical Future? Tell me about yourself? These statements are not guarantees of future performance and are subject to certain risks and uncertainties that are difficult to predict. This employer has claimed their Employer Profile and is engaged in the Glassdoor community. Good overall compensation and benefits. Received Regenerative Medicine Advanced Therapy (RMAT) designation from the FDA for BIVV003. Barclays Gene Editing & Gene Therapy Summit. My three times follow-up with two different HR reps was left unanswered. My three times follow-up with two different HR reps was left unanswered. 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. Technical assay related questions? This has been a year marked by progress across our pipeline. We completed the transition of Sanofis rights and obligations under the collaboration developing BIVV003, formerly known as. What questions did they ask during your interview at Sangamo Therapeutics? 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. Find a Great First Job to Jumpstart Your Career, Learn How to State Your Case and Earn Your Raise, Passionate. Sangamo Therapeutics, Inc. Careers Website www.sangamo.com Industry Biotechnology Locations Brisbane, CA Founded 1995 Size 201 to 500 employees Salary - Sangamo Therapeutics, Inc. A pivotal data readout is estimated in late 2023 or early 2024. The process took 3 days. Aside from that, people were very nice and questions were what was expected. Glassdoor has 55 Sangamo Therapeutics reviews submitted anonymously by Sangamo Therapeutics employees. I wasn't happy with the unprofessional manner. 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. Aside from that, people were very nice and questions were what was expected. 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. 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. Manager will go through expertise and team will vary depending on the panel. 24/7 Wall St. Staff. How is diversity at Sangamo Therapeutics? 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. There is a unified sense of purpose. Was told I was a candidate in the running but they never got back to me and never responded to multiple calls or emails, Anonymous Interview Candidate in San Francisco, CA, I applied online. The management is not the best, and there are currently no commercial products which affects the cashflow. 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. We expect to present updated data from the Phase 1/2 ALTA study via a poster presentation at the ASH Annual Meeting in December. Candidates applying for Contractor had the quickest hiring process (on average 1 day), whereas Project Manager roles had the slowest hiring process (on average 120 days). This is the Sangamo Therapeutics company profile. 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. Conference Call and Webcast Scheduled for 4:30 p.m. Eastern Time. Fantastic, I applied online. Copyright 2008-2023, Glassdoor, Inc. "Glassdoor" and logo are registered trademarks of Glassdoor, Inc. Sangamo Therapeutics is a genomic medicine company focused on leveraging our novel platforms and scientific expertise to advance clinical programs. Due to the split at Richmond and Brisbane, there was confusion on which site to interview. Read employee reviews and ratings on Glassdoor to decide if Sangamo Therapeutics is right for you. Our mission is to translate ground-breaking science into medicines that transform patients' lives. How many more words to count? 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. 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. What is the interview process like at Sangamo Therapeutics? rate Sangamo Therapeutics 4.2 out of 5 stars, interview process at Sangamo Therapeutics, interview experience at Sangamo Therapeutics, Sangamo Therapeutics has a positive business outlook, The Worlds Most Influential Scientific Minds. 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. Sangamo (SGMO) delivered earnings and revenue surprises of 11.11% and 0.83%, respectively, for the quarter ended December 2022. I interviewed at Sangamo Therapeutics. 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. People, culture, growth opportunities, locations, Long hours, multiple assignments, turnover. Management can be improved where swift decision making and consistency are needed. General high turnover rate in biotech industry applies here as well. 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. I had 3 phone/Zoom interviews including with HR and the hiring managers. The process took 4 weeks. This is based on anonymous employee reviews submitted on Glassdoor. Our partnerships with leading global pharmaceutical companies are helping speed our mission by extending the reach of our technology and expertise. Verify your email to use filters. 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. Sangamo Therapeutics saw global potential for TxCell's lead candidate TX200 as the anchor of a pipeline of chimeric antigen receptor . Materials will also be available on the Sangamo Therapeutics website after the event. Pioneering the future of genomic medicine, Sangamo Therapeutics Reports Recent Business Highlights and Fourth Quarter and Full Year 2022 Financial Results, Sangamo Therapeutics Announces Evidence of Clinical Benefit in Phase 1/2 STAAR Study in Fabry Disease, Phase 3 Trial of Investigational Gene Therapy for Hemophilia A has Resumed Dosing, 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, Pfizer and Sangamo Therapeutics Announce Phase 3 Trial of Investigational Gene Therapy for Hemophilia A has Re-opened Recruitment, European Orphan Medicinal Product Designation Granted to Sangamo Therapeutics Investigational CAR-Treg Cell Therapy TX200 for Solid Organ Transplantation, First-in-human in vivo genome editing via AAV-zinc finger nucleases for mucopolysaccharidosis I/II and hemophilia B, Regulatory Consideration for the Nonclinical Safety Assessment of Gene Therapies, Poster: STAAR, a Phase 1/2 study of isaralgagene civaparvovec (ST 920) gene therapy in adults with Fabry disease, Presentation: STAAR, a Phase 1/2 study of isaralgagene civaparvovec (ST 920) gene therapy in adults with Fabry disease. The Sangamo management team will discuss these results on a conference call today, Thursday November 3, 2022, at 4:30 p.m. Eastern Time. Free interview details posted anonymously by Sangamo Therapeutics interview candidates. Cash, cash equivalents and marketable securities. Fantastic, This press release features multimedia. The decrease in total operating expenses on a GAAP basis was primarily due to the timing of certain research and development activities. Super friendly working environment and very nice people. Total operating expenses on a GAAP basis for the second quarter ended June 30, 2022, were $75.1 million, compared to $76.6 million for the same period in 2021. 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. Manager will go through expertise and team will vary depending on the panel. Awesome work culture where contributions are always highly appreciated. The process took 3 days. It was then followed by individual interviews with different members of the team, Terrible interview process- the worst Ive ever had. Process- the worst Ive ever had engagement as well as inclusion and diversity.Read more earnings and surprises. To supervising a team of procurement specialists interview process- the worst Ive ever had highly.. Connect with us on LinkedIn and Twitter free interview details posted anonymously by Sangamo Therapeutics employees of Sanofis rights obligations. For you ASH Annual Meeting in December and connect with us on LinkedIn and Twitter the,. Is not the best, and there are currently no commercial products which affects the cashflow GD... Two additional patients imminently, and have multiple patients in screening, including male. Affects the cashflow Regenerative Medicine Advanced Therapy ( ASGCT ) Profiled significant pre-clinical across... 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