Home › Companies › Iblyjb Fa Ocs Oraclecloud Com CX 2001 › Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must
Iblyjb Fa Ocs Oraclecloud Com CX 2001 · United States; United States - Remote - Eastern Time, Cambridge, MA, US · Hybrid · Active · Oracle Recruiting Cloud / Fusion HCM
Job facts
| Field | Value |
|---|---|
| Company | Iblyjb Fa Ocs Oraclecloud Com CX 2001 |
| Title | Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must |
| Normalized title | - |
| Department / team | Statistical Programming - FSP |
| Location | United States |
| Work model | Hybrid / Hybrid |
| Employment type | Full Time |
| Salary | - |
| Status | active |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
| Posted / first seen | 2026-05-14 / 2026-05-31 |
| Changed / last seen | 2026-05-31 / 2026-06-06 |
Related slices
| Page | What it contains | Open |
|---|---|---|
| Company jobs | Active postings from Iblyjb Fa Ocs Oraclecloud Com CX 2001. | Open |
| Company breakdowns | Role, location, ATS, and work model facets for this company. | Open |
| ATS provider jobs | Active postings observed through Oracle Recruiting Cloud / Fusion HCM. | Open |
| Provider filtered search | The same provider as a filtered job collection. | Open |
| Department jobs | Active postings in Statistical Programming - FSP. | Open |
| Work model jobs | Active Hybrid postings. | Open |
| Lifecycle events | Open, update, close, and reopen events for this posting. | Open |
| Original posting | Canonical source or apply URL captured from the ATS. | Open |
Linked records
| Company | Iblyjb Fa Ocs Oraclecloud Com CX 2001 |
| Source | 118dd8bd-c51f-43c2-93a6-817304220200 |
| ATS provider | Oracle Recruiting Cloud / Fusion HCM |
Description
Description
Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
Position Overview:
As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Early or Late-stage clinical trials. This role is Hybrid office based in PA (Preferred) OR NJ .
Our values We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology.
Responsibilities
How you will contribute:
Generating and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Production and QC / validation programming Generating complex ad-hoc reports utilizing raw data Applying strong understanding/experience of Efficacy analysis Creating and reviewing submission documents and eCRTs Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries Performing lead duties when called upon Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Being adaptable and flexible when priorities change
Qualifications
Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have:
Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc. At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above. Having experience/expertise working on Early Development studies. Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters). Develop and validate global programming standards for ADaM datasets. Develop and validate global programming standards for efficacy analysis, safety analysis and reporting. Design and develop complex programming algorithms. Experience in one or more of the following will be preferred: R, SPlus, NonMem. Assist project teams in creating SDTM deliverables for Analysis and Reporting (A&R) and submission. Support project teams in preparing submission deliverables including use of Pinnacle 21 Enterprise. Up-versioning activities to specific versions of SDTM. Experience supporting Oncology studies would be a plus. Strong SAS data manipulation, analysis and reporting skills. Solid experience implementing the latest CDISC SDTM / ADaM standards. Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data. Submissions experience utilizing define.xml and other submission documents. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
Full job record
| Job ID | 11685599339e36cdd757db56ce89c5502cfdbd05 |
| Org ID | 1db7e607-b344-4109-abb0-4cfac49e25b6 |
| Source ID | 118dd8bd-c51f-43c2-93a6-817304220200 |
| Board ID | 118dd8bd-c51f-43c2-93a6-817304220200 |
| Provider | oracle_hcm |
| Provider Job Key | 1534 |
| Title | Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must |
| Normalized Title | — |
| Status | active |
| Active | yes |
| Location Text | United States; United States - Remote - Eastern Time, Cambridge, MA, US |
| Department | Statistical Programming - FSP |
| Team | — |
| Employment Type | full_time |
| Workplace Type | hybrid |
| Remote Policy | hybrid |
| Country | United States |
| Region | — |
| City | — |
| Salary Raw | Description Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview: As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Early or Late-stage clinical trials. This role is Hybrid office based in PA (Preferred) OR NJ . Our values We believe in applying scientific rigor to reveal the full promise inherent in data. We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. We prize innovation and seek intelligent solutions using leading-edge technology. Responsibilities How you will contribute: Generating and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming Production and QC / validation programming Generating complex ad-hoc reports utilizing raw data Applying strong understanding/experience of Efficacy analysis Creating and reviewing submission documents and eCRTs Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries Performing lead duties when called upon Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc. Being adaptable and flexible when priorities change Qualifications Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc. At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above. Having experience/expertise working on Early Development studies. Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters). Develop and validate global programming standards for ADaM datasets. Develop and validate global programming standards for efficacy analysis, safety analysis and reporting. Design and develop complex programming algorithms. Experience in one or more of the following will be preferred: R, SPlus, NonMem. Assist project teams in creating SDTM deliverables for Analysis and Reporting (A&R) and submission. Support project teams in preparing submission deliverables including use of Pinnacle 21 Enterprise. Up-versioning activities to specific versions of SDTM. Experience supporting Oncology studies would be a plus. Strong SAS data manipulation, analysis and reporting skills. Solid experience implementing the latest CDISC SDTM / ADaM standards. Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF. Strong QC / validation skills. Good ad-hoc reporting skills. Proficiency in Efficacy analysis. Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data. Submissions experience utilizing define.xml and other submission documents. Excellent analytical & troubleshooting skills. Ability to provide quality output and deliverables, in adherence with challenging timelines. Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners. |
| Salary Min | — |
| Salary Max | — |
| Salary Currency | — |
| Salary Period | — |
| Source URL | https://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1534 |
| Apply URL | https://iblyjb.fa.ocs.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/1534 |
| First Seen At | 2026-05-31 17:57:23Z |
| Last Seen At | 2026-06-06 19:15:54Z |
| Last Checked At | 2026-06-06 19:15:54Z |
| Last Changed At | 2026-05-31 17:57:23Z |
| Inactive At | — |
| Source Posted At | 2026-05-14 15:27:54Z |
| Source Updated At | — |
| Raw Payload Uri | s3://job-postings-prod-raw-590183727216/raw/provider=oracle_hcm/board=iblyjb.fa.ocs.oraclecloud.com|CX_2001/date=2026-06-06/2026-06-06T19-15-49-308Z-ccec882a74e70930a7c702c819603e19e4aed30447df56282a6570cecb0240df.json |
Event Fields
{
"content_hash": "0011c9e45c3a591e89349e8a54eb630fcdeacf88e9ac8b9225be3b8768486431",
"source_hash": "dea2bc1cca0118d5bd16a85c14562cf480d59cf3c9ebbfb35ca3d112c50057c0",
"last_changed_at": "2026-05-31T17:57:23.428Z",
"active_status": "active"
}Parsed Structured
{
"language": "en",
"location": {
"raw": "United States",
"city": null,
"region": null,
"country": "United States",
"is_remote": false,
"confidence": 0.8
},
"salary_max": null,
"salary_min": null,
"inferred_at": "2026-06-06T19:15:54.074Z",
"launch_scope": {
"reason": "english_us_canada",
"included": true,
"language": "en",
"location": {
"raw": "United States",
"city": null,
"region": null,
"country": "United States",
"is_remote": false,
"confidence": 0.8
},
"countries": [
"United States"
]
},
"remote_policy": "hybrid",
"salary_period": null,
"workplace_type": "hybrid",
"salary_currency": null
}Extensions
{}Native Structured
{
"detail": {
"Id": "1534",
"Title": "Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must",
"media": [],
"skills": [],
"JobType": null,
"Category": "Statistical Programming - FSP",
"JobGrade": null,
"JobLevel": null,
"JobShift": null,
"WorkDays": null,
"WorkHours": null,
"WorkYears": null,
"Department": null,
"HotJobFlag": false,
"StudyLevel": null,
"WorkMonths": null,
"WorkerType": null,
"GeographyId": 300000000468633,
"JobFamilyId": 300000005587713,
"JobFunction": "Statistical Programming",
"JobSchedule": "Full time",
"BusinessUnit": null,
"ContractType": null,
"Organization": null,
"TrendingFlag": false,
"workLocation": [
{
"Country": "US",
"Region1": "Middlesex",
"Region2": "MA",
"Region3": null,
"Building": null,
"Latitude": "42.36471",
"Longitude": "-71.1042",
"LocationId": 300000006095412,
"PostalCode": "02139",
"TownOrCity": "Cambridge",
"AddressLine1": "Remote",
"AddressLine2": null,
"AddressLine3": null,
"AddressLine4": null,
"LocationName": "United States - Remote - Eastern Time"
}
],
"ContentLocale": "en",
"HiringManager": null,
"LegalEmployer": null,
"RequisitionId": 300000086607591,
"WorkplaceType": "Hybrid",
"BusinessUnitId": 300000005454386,
"OrganizationId": 1,
"GeographyNodeId": 300000005464575,
"JobFunctionCode": "Statistical Programming",
"LegalEmployerId": 300000005464001,
"PrimaryLocation": "United States",
"RequisitionType": "Professional",
"NumberOfOpenings": null,
"WorkplaceTypeCode": "ORA_HYBRID",
"BeFirstToApplyFlag": false,
"otherWorkLocations": [],
"secondaryLocations": [],
"ExternalContactName": null,
"ShortDescriptionStr": "Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.",
"ExternalContactEmail": null,
"ExternalPostedEndDate": null,
"OtherRequisitionTitle": null,
"requisitionFlexFields": [],
"ApplyWhenNotPostedFlag": false,
"DomesticTravelRequired": null,
"ExternalDescriptionStr": "<div><div><strong>Sponsor-dedicated:</strong></div><div> </div><div>Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer, you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.</div><div><br> </div><div><strong>Position Overview: </strong></div><div><br> </div><div>As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Early or Late-stage clinical trials. <strong>This role is Hybrid office based in PA (Preferred) OR NJ</strong>.</div></div><div><br> </div><div><div><strong>Our values</strong></div><div><ul><li>We believe in applying scientific rigor to reveal the full promise inherent in data.</li><li>We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.</li><li>We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.</li><li>We prize innovation and seek intelligent solutions using leading-edge technology.</li></ul></div></div>",
"ObjectVerNumberProfile": null,
"PrimaryLocationCountry": "US",
"CorporateDescriptionStr": "",
"ExternalPostedStartDate": "2026-05-14T15:27:54+00:00",
"ExternalQualificationsStr": "<p><strong>Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: </strong> </p><div><ul><li>Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.</li><li>At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.</li><li><strong>Having experience/expertise working on Early Development studies. Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters).</strong></li><li>Develop and validate global programming standards for ADaM datasets.</li><li>Develop and validate global programming standards for efficacy analysis, safety analysis and reporting.</li><li>Design and develop complex programming algorithms.</li><li>Experience in one or more of the following will be preferred: R, SPlus, NonMem.</li><li>Assist project teams in creating SDTM deliverables for Analysis and Reporting (A&R) and submission.</li><li>Support project teams in preparing submission deliverables including use of Pinnacle 21 Enterprise.</li><li>Up-versioning activities to specific versions of SDTM.</li><li>Experience supporting Oncology studies would be a plus.</li><li>Strong SAS data manipulation, analysis and reporting skills.</li><li>Solid experience implementing the latest CDISC SDTM / ADaM standards.</li><li>Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF.</li><li>Strong QC / validation skills.</li><li>Good ad-hoc reporting skills. </li><li>Proficiency in Efficacy analysis.</li><li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.</li><li>Submissions experience utilizing define.xml and other submission documents.</li><li>Excellent analytical & troubleshooting skills.</li><li>Ability to provide quality output and deliverables, in adherence with challenging timelines.</li><li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.</li></ul></div>",
"InternalQualificationsStr": "<p><strong>Here at Cytel we want our employees to succeed and we enable this success through consistent training, development and support. To be successful in this position you will have: </strong> </p><div><ul><li>Bachelor’s degree in one of the following fields Statistics, Computer Science, Mathematics, etc.</li><li>At least 8 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor’s degree or equivalent. At least 6 years of related experience with a master’s degree or above.</li><li><strong>Having experience/expertise working on Early Development studies. Programming expertise with clinical endpoint data (efficacy and safety) and pharmacokinetic data (raw concentration data, derived PK parameters).</strong></li><li>Develop and validate global programming standards for ADaM datasets.</li><li>Develop and validate global programming standards for efficacy analysis, safety analysis and reporting.</li><li>Design and develop complex programming algorithms.</li><li>Experience in one or more of the following will be preferred: R, SPlus, NonMem.</li><li>Assist project teams in creating SDTM deliverables for Analysis and Reporting (A&R) and submission.</li><li>Support project teams in preparing submission deliverables including use of Pinnacle 21 Enterprise.</li><li>Up-versioning activities to specific versions of SDTM.</li><li>Experience supporting Oncology studies would be a plus.</li><li>Strong SAS data manipulation, analysis and reporting skills.</li><li>Solid experience implementing the latest CDISC SDTM / ADaM standards.</li><li>Knowledge of submission standards CDISC SDTM, Define.XML, SDRG, aCRF.</li><li>Strong QC / validation skills.</li><li>Good ad-hoc reporting skills. </li><li>Proficiency in Efficacy analysis.</li><li>Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials’ data.</li><li>Submissions experience utilizing define.xml and other submission documents.</li><li>Excellent analytical & troubleshooting skills.</li><li>Ability to provide quality output and deliverables, in adherence with challenging timelines.</li><li>Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.</li></ul></div>",
"OrganizationDescriptionStr": "",
"primaryLocationCoordinates": [
{
"Latitude": "39.82844",
"Longitude": "-98.57939",
"CountryCode": "US",
"GeographyId": 300000000468633,
"GeographyNodeId": 300000005464575
}
],
"ExternalResponsibilitiesStr": "<p><strong>How you will contribute:</strong></p><p> </p><ul><li>Generating and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas</li><li>Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming</li><li>Production and QC / validation programming</li><li>Generating complex ad-hoc reports utilizing raw data</li><li>Applying strong understanding/experience of Efficacy analysis</li><li>Creating and reviewing submission documents and eCRTs</li><li>Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries</li><li>Performing lead duties when called upon</li><li>Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.</li><li>Being adaptable and flexible when priorities change</li></ul>",
"InternalResponsibilitiesStr": "<p><strong>How you will contribute:</strong></p><p> </p><ul><li>Generating and validating statistical programming deliverables (SDTM, ADAM, TFL's) in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas</li><li>Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy (ISS/ISE), utilizing SAS programming</li><li>Production and QC / validation programming</li><li>Generating complex ad-hoc reports utilizing raw data</li><li>Applying strong understanding/experience of Efficacy analysis</li><li>Creating and reviewing submission documents and eCRTs</li><li>Communicating with and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries</li><li>Performing lead duties when called upon</li><li>Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.</li><li>Being adaptable and flexible when priorities change</li></ul>",
"InternationalTravelRequired": null
},
"list_job": {
"Id": "1534",
"Title": "Senior Statistical Programmer FSP-Hybrid 3 days a week in PA a must",
"JobType": null,
"Distance": 1778716800000,
"JobShift": null,
"Language": "US",
"WorkDays": null,
"JobFamily": null,
"Relevancy": 2,
"WorkHours": null,
"Department": null,
"HotJobFlag": false,
"PostedDate": "2026-05-14",
"StudyLevel": null,
"WorkerType": null,
"GeographyId": 300000000468633,
"JobFunction": null,
"JobSchedule": null,
"BusinessUnit": null,
"ContractType": null,
"ManagerLevel": null,
"Organization": null,
"TrendingFlag": false,
"workLocation": [
{
"Country": "US",
"Region1": "Middlesex",
"Region2": "MA",
"Region3": null,
"Building": null,
"Latitude": 42.36471,
"Longitude": -71.1042,
"LocationId": 300000006095412,
"PostalCode": "02139",
"TownOrCity": "Cambridge",
"AddressLine1": "Remote",
"AddressLine2": null,
"AddressLine3": null,
"AddressLine4": null,
"LocationName": "United States - Remote - Eastern Time"
}
],
"LegalEmployer": null,
"MediaThumbURL": null,
"WorkplaceType": "Hybrid",
"BusinessUnitId": 300000005454386,
"OrganizationId": 1,
"PostingEndDate": null,
"LegalEmployerId": 300000005464001,
"PrimaryLocation": "United States",
"WorkDurationYears": null,
"WorkplaceTypeCode": "ORA_HYBRID",
"BeFirstToApplyFlag": false,
"WorkDurationMonths": null,
"otherWorkLocations": [],
"secondaryLocations": [],
"ShortDescriptionStr": "Our commitment to developing our staff is only surpassed by our commitment to advancing treatment options available to patients. At Cytel, we work hard to create successful careers with significant professional growth for our employees and as a result work hard to make Cytel successful. Cytel is a place where talent, experience, and integrity come together to advance the state of clinical development.",
"requisitionFlexFields": [],
"DomesticTravelRequired": null,
"PrimaryLocationCountry": "US",
"ExternalQualificationsStr": null,
"ExternalResponsibilitiesStr": null,
"InternationalTravelRequired": null
},
"detail_meta": {
"url": "https://iblyjb.fa.ocs.oraclecloud.com/hcmRestApi/resources/latest/recruitingCEJobRequisitionDetails?expand=all&onlyData=true&finder=ById;Id=%221534%22,siteNumber=CX_2001",
"http_status": 200,
"content_type": "application/json",
"response_bytes": 11810
},
"detail_errors": []
}Get this page with API
Rendered from the bluedoor Job Postings API. Reproduce it:
GET https://api.bluedoor.sh/job-postings/v1/jobs/11685599339e36cdd757db56ce89c5502cfdbd05?include=descriptionJSONGET https://api.bluedoor.sh/job-postings/v1/orgs/1db7e607-b344-4109-abb0-4cfac49e25b6JSONGET https://api.bluedoor.sh/job-postings/v1/sources/118dd8bd-c51f-43c2-93a6-817304220200JSONGET https://api.bluedoor.sh/job-postings/v1/jobs/11685599339e36cdd757db56ce89c5502cfdbd05/eventsJSON