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HomeCompaniesZailabusllc1Senior Clinical Trial Manager (Office Based - South SF 3X/wk)

Senior Clinical Trial Manager (Office Based - South SF 3X/wk)

Zailabusllc1 · South San Francisco, CA, United States · Hybrid · Deleted · $177,000–$229,000 / year · SmartRecruiters

Job facts

FieldValue
CompanyZailabusllc1
TitleSenior Clinical Trial Manager (Office Based - South SF 3X/wk)
Normalized title-
Department / teamClinical Ops
LocationSouth San Francisco, CA, United States
Work modelHybrid / Hybrid
Employment typeFull Time
Salary$177,000–$229,000 / year
Statusdeleted
ATS providerSmartRecruiters
Posted / first seen2026-03-13 / 2026-05-31
Changed / last seen2026-06-18 / 2026-06-16

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PageWhat it containsOpen
Company jobsActive postings from Zailabusllc1.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through SmartRecruiters.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in South San Francisco.Open
Department jobsActive postings in Clinical Ops.Open
Work model jobsActive Hybrid postings.Open
Lifecycle eventsOpen, update, close, and reopen events for this posting.Open
Original postingCanonical source or apply URL captured from the ATS.Open

Linked records

CompanyZailabusllc1
Sourcec6d48162-ec83-4edd-a3ec-c89b59e56f96
ATS providerSmartRecruiters

Description

Zai Lab Limited (NASDAQ: ZLAB; HKEX: 9688) is an innovative, research-based, commercial-stage biopharmaceutical company based in China and the United States focused on bringing transformative medicines for oncology, autoimmune disorders, infectious diseases, and neurological disorders to patients in China and around the world. Our goal is to leverage our competencies and resources to positively impact human health worldwide. Founded in 2014, our experienced team has secured partnerships with leading global biopharmaceutical  companies, generating a broad and late-stage pipeline of innovative drug candidates. Based on our proven  track record of  success, Zai Lab has earned the reputation as a trusted partner of choice for global biopharmaceutical companies seeking to not only access the Chinese market but also find a long-term strategic partner for global clinical development.  Our unique business model builds on our in-licensed assets and innovative partnerships to expand our internal discovery and development capabilities and has created a portfolio of potential best-in-class and/or first-in-class therapies. Zai currently has four products on the market in China Zai Lab was successfully listed on the Nasdaq Stock Market in September 2017 and completed secondary listing on Hong Kong Stock Exchange in September 2020. In 2022, Zai Lab became dual-primary listed on both the Nasdaq and the Hong Kong Stock Exchanges. Since its inception, Zai Lab has expanded significantly with several offices across China. In 2021, Zai Lab established its U.S. Headquarters in Cambridge, Massachusetts.  As of January 2022, the Company has a global team of approximately 2000 employees. The Senior Clinical Trial Manager will lead, manage and co-ordinate the operational strategy, risk management, and overall execution of clinical trials from study start-up to close out at a global level in accordance with ICH-GCP and applicable local regulations. Collaborate with cross functional stakeholders to ensure deliverables are met in terms of quality, compliance, budget, and timing. This role may work collaboratively on one trial or across several trials to support clinical operations activities. This position is based in our South San Francisco, CA office. Lead and coordinate a cross-functional study team to ensure the clinical trial progresses as planned. Accountable for the overall operational strategy and delivery (e.g., country and site selection/start-up, site contracts, patient recruitment and retention, etc.) of assigned clinical trials; ensuring that study-level deliverables are met according to timeline, budget, and quality requirements. Participates in developing and finalizing cross-functional activities to ensure delivery of critical clinical trial documents such as informed consent forms (ICFs), protocols, site and country budget templates, EDC, IxRS, central/specialty lab, ECG, imaging, PRO specifications, drug supply, biomarker/sample management plans, TMF, and CSRs. Drafts and implements study plans including; vendor oversight, risk, quality, safety, communication, trial monitoring, and TMF. Ensures TMF creation and QC completion. Supports EDC, IxRS, and CTMS systems and data maintenance. Tracks budget, timelines, milestones, and critical study activities, identifies issues and proposes potential resolutions. Accountable for the study budget and manages assigned vendor budget(s); communicates variances in actual versus forecasted spend in vendor budgets and presents an action plan for resolution. Drives the selection of vendors (participates in the Request for Proposal (RFP) process) on a global scale. Oversees delegated outsourced activities to ensure CRO and vendor delivery against the contracted scope of work. Leads the Investigator Meeting preparation and execution with the support from cross-functional team members Stays current on relevant therapeutic area knowledge and clinical research best practices. Ensures study adherence to ICH/GCP and company SOPs. REQUIRED: Undergraduate degree in a scientific or health-related discipline. Minimum of 8 years relevant experience of which 5 years are clinical experience in the pharmaceutical industry, including 3 years in study management or equivalent combination of education, training, and experience. Ability to work across several time zones. PREFERRED: Prior people management experience. Demonstrated ability in clinical study management processes and clinical/drug development. Highly effective verbal and written communication skills; effectively deliver key messages; aptitude to independently communicate with teams and stakeholders. Ability to effectively lead projects and persuade and influence peers; ability to build trusting and collaborative relationships globally. Experience with effective vendor management. Strong customer focus with investigators, functional peers, vendors, etc. Excellent planning and organizational skills. Working knowledge of international regulatory and ICH Good Clinical Practice guidelines. Maintains the highest standards of integrity and ethics. The pay range for this position at commencement of employment is expected to be between $177K and $229K/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. At Zai, we are proud of the gender diversity of our company and our promotion of women in biotech. We have achieved gender base pay equity at all levels, 58% of our employees are women and 54% of our management positions are held by women. We are committed to the health of patients and our planet. That’s why our environmental protection, social responsibility, and corporate governance strategy, called “Trust for Life” is integrated within our business. Disclaimer: This description is not intended to be construed as an exhaustive list of duties, responsibilities, or requirement for the position. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or based on disability. Zai Lab is committed to protecting the privacy and security of the information we collect and to being transparent about the purposes for which we use your information. We have a  Privacy Notice  which sets forth our policies and practices for handling the information we collect and use in the employment context.  Privacy Notice available upon request.

Full job record

Job IDd5171374add07b1623deeaba4c48ff333a0eb000
Org IDbfbd0547-f092-4da1-8b3d-1e2a7a5a2c1d
Source IDc6d48162-ec83-4edd-a3ec-c89b59e56f96
Board IDc6d48162-ec83-4edd-a3ec-c89b59e56f96
Providersmartrecruiters
Provider Job Key744000114725775
TitleSenior Clinical Trial Manager (Office Based - South SF 3X/wk)
Normalized Title
Statusdeleted
Activeno
Location TextSouth San Francisco, CA, United States
DepartmentClinical Ops
Team
Employment Typefull_time
Workplace Typehybrid
Remote Policyhybrid
CountryUnited States
RegionCA
CitySouth San Francisco
Salary RawZai Lab Limited (NASDAQ: ZLAB; HKEX: 9688) is an innovative, research-based, commercial-stage biopharmaceutical company based in China and the United States focused on bringing transformative medicines for oncology, autoimmune disorders, infectious diseases, and neurological disorders to patients in China and around the world. Our goal is to leverage our competencies and resources to positively impact human health worldwide. Founded in 2014, our experienced team has secured partnerships with leading global biopharmaceutical  companies, generating a broad and late-stage pipeline of innovative drug candidates. Based on our proven  track record of  success, Zai Lab has earned the reputation as a trusted partner of choice for global biopharmaceutical companies seeking to not only access the Chinese market but also find a long-term strategic partner for global clinical development.  Our unique business model builds on our in-licensed assets and innovative partnerships to expand our internal discovery and development capabilities and has created a portfolio of potential best-in-class and/or first-in-class therapies. Zai currently has four products on the market in China Zai Lab was successfully listed on the Nasdaq Stock Market in September 2017 and completed secondary listing on Hong Kong Stock Exchange in September 2020. In 2022, Zai Lab became dual-primary listed on both the Nasdaq and the Hong Kong Stock Exchanges. Since its inception, Zai Lab has expanded significantly with several offices across China. In 2021, Zai Lab established its U.S. Headquarters in Cambridge, Massachusetts.  As of January 2022, the Company has a global team of approximately 2000 employees. The Senior Clinical Trial Manager will lead, manage and co-ordinate the operational strategy, risk management, and overall execution of clinical trials from study start-up to close out at a global level in accordance with ICH-GCP and applicable local regulations. Collaborate with cross functional stakeholders to ensure deliverables are met in terms of quality, compliance, budget, and timing. This role may work collaboratively on one trial or across several trials to support clinical operations activities. This position is based in our South San Francisco, CA office. Lead and coordinate a cross-functional study team to ensure the clinical trial progresses as planned. Accountable for the overall operational strategy and delivery (e.g., country and site selection/start-up, site contracts, patient recruitment and retention, etc.) of assigned clinical trials; ensuring that study-level deliverables are met according to timeline, budget, and quality requirements. Participates in developing and finalizing cross-functional activities to ensure delivery of critical clinical trial documents such as informed consent forms (ICFs), protocols, site and country budget templates, EDC, IxRS, central/specialty lab, ECG, imaging, PRO specifications, drug supply, biomarker/sample management plans, TMF, and CSRs. Drafts and implements study plans including; vendor oversight, risk, quality, safety, communication, trial monitoring, and TMF. Ensures TMF creation and QC completion. Supports EDC, IxRS, and CTMS systems and data maintenance. Tracks budget, timelines, milestones, and critical study activities, identifies issues and proposes potential resolutions. Accountable for the study budget and manages assigned vendor budget(s); communicates variances in actual versus forecasted spend in vendor budgets and presents an action plan for resolution. Drives the selection of vendors (participates in the Request for Proposal (RFP) process) on a global scale. Oversees delegated outsourced activities to ensure CRO and vendor delivery against the contracted scope of work. Leads the Investigator Meeting preparation and execution with the support from cross-functional team members Stays current on relevant therapeutic area knowledge and clinical research best practices. Ensures study adherence to ICH/GCP and company SOPs. REQUIRED: Undergraduate degree in a scientific or health-related discipline. Minimum of 8 years relevant experience of which 5 years are clinical experience in the pharmaceutical industry, including 3 years in study management or equivalent combination of education, training, and experience. Ability to work across several time zones. PREFERRED: Prior people management experience. Demonstrated ability in clinical study management processes and clinical/drug development. Highly effective verbal and written communication skills; effectively deliver key messages; aptitude to independently communicate with teams and stakeholders. Ability to effectively lead projects and persuade and influence peers; ability to build trusting and collaborative relationships globally. Experience with effective vendor management. Strong customer focus with investigators, functional peers, vendors, etc. Excellent planning and organizational skills. Working knowledge of international regulatory and ICH Good Clinical Practice guidelines. Maintains the highest standards of integrity and ethics. The pay range for this position at commencement of employment is expected to be between $177K and $229K/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. At Zai, we are proud of the gender diversity of our company and our promotion of women in biotech. We have achieved gender base pay equity at all levels, 58% of our employees are women and 54% of our management positions are held by women. We are committed to the health of patients and our planet. That’s why our environmental protection, social responsibility, and corporate governance strategy, called “Trust for Life” is integrated within our business. Disclaimer: This description is not intended to be construed as an exhaustive list of duties, responsibilities, or requirement for the position. All personnel may be required to perform duties outside of their normal responsibilities from time to time, as needed. All qualified applicants will receive consideration for employment without regard to race, sex, color, religion, sexual orientation, gender identity, national origin, protected veteran status, or based on disability. Zai Lab is committed to protecting the privacy and security of the information we collect and to being transparent about the purposes for which we use your information. We have a  Privacy Notice  which sets forth our policies and practices for handling the information we collect and use in the employment context.  Privacy Notice available upon request.
Salary Min177,000
Salary Max229,000
Salary CurrencyUSD
Salary Periodyear
Source URLhttps://jobs.smartrecruiters.com/ZaiLabUSLLC1/744000114725775-senior-clinical-trial-manager-office-based-south-sf-3x-wk-
Apply URLhttps://jobs.smartrecruiters.com/ZaiLabUSLLC1/744000114725775-senior-clinical-trial-manager-office-based-south-sf-3x-wk-?oga=true
First Seen At2026-05-31 17:43:37Z
Last Seen At2026-06-16 11:46:00Z
Last Checked At2026-06-18 10:56:10Z
Last Changed At2026-06-18 10:56:10Z
Inactive At2026-06-18 10:56:10Z
Source Posted At2026-03-13 17:51:04Z
Source Updated At
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Extensions
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Rendered from the bluedoor Job Postings API. Reproduce it:

GET https://api.bluedoor.sh/job-postings/v1/jobs/d5171374add07b1623deeaba4c48ff333a0eb000?include=descriptionJSON
GET https://api.bluedoor.sh/job-postings/v1/orgs/bfbd0547-f092-4da1-8b3d-1e2a7a5a2c1dJSON
GET https://api.bluedoor.sh/job-postings/v1/sources/c6d48162-ec83-4edd-a3ec-c89b59e56f96JSON
GET https://api.bluedoor.sh/job-postings/v1/jobs/d5171374add07b1623deeaba4c48ff333a0eb000/eventsJSON