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Clinical Trials Associate - Japanese Speaking

Richmondpharm · London, Southwark, SE1 1YR, United Kingdom · Active · BambooHR

Job facts

FieldValue
CompanyRichmondpharm
TitleClinical Trials Associate - Japanese Speaking
Normalized title-
Department / teamClinical Operations
LocationLondon, Southwark
Work model-
Employment typeContract
Salary-
Statusactive
ATS providerBambooHR
Posted / first seen2026-02-18 / 2026-05-30
Changed / last seen2026-05-30 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Richmondpharm.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through BambooHR.Open
Provider filtered searchThe same provider as a filtered job collection.Open
City jobsActive postings in London.Open
Department jobsActive postings in Clinical Operations.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

CompanyRichmondpharm
Source2015ec9c-642c-4c8a-beff-a51e3acad478
ATS providerBambooHR

Description

Title: Clinical Trials Associate - Japanese Speaking Location: London Bridge, London Term: 12-month FTC, Full Time Salary: £27,000 + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays & many more) Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), where we are conducting pioneering early phase healthy participants and patient participant trials. Our experienced and world-renowned team, our central London location and our global reach contribute to making Richmond Pharmacology an exciting and dynamic place to work. A new opportunity has opened at Richmond Pharmacology for a Clinical Trials Associate to join a specialised team providing clinical support to Research Physicians and volunteers taking part in the trials of innovative new therapies. This is an entry level role with a career path focused on development of clinical excellence in the delivery of a variety of Phase I-III clinical trials. Key tasks will include specific clinical procedures, ward rounds, ward maintenance, volunteer support and document management. Full training will be provided and candidates will be expected to pass assessments for key skills and maintain these to a high standard throughout. Requirements Previous experience working as a Healthcare Assistant Excellent communication skills and an engaging manner High energy, proactive and enthusiastic High attention to detail Available to work shifts (early, standard, late, night) including occasional weekends Customer service or hospitality sector experience would be attractive Successful candidates will need to pass DBS checks Key Tasks Clinical - phlebotomy, ECG, vitals etc - training in all procedures provided Documentation - study specific documents, from point of collection to quality checking Sample collection - efficient, safe collection of samples from volunteers including accurate labelling and management Volunteer support - looking after the needs and monitoring the safety of volunteers within the ward environment – Immediate Life Support (ILS) training provided Ward maintenance - ensuring the wards are clean, tidy and properly stocked for the care of volunteers Queries - raising queries and assisting in the resolution of queries to ensure study requirements are delivered appropriately As well as working daily with volunteers, you will need to interact effectively with all other departments internally and provide an efficient service to support the delivery of clinical trials. You will need to familiarise yourself with all SOP's for working within the business, as well as all details specific to the trials you will be working on. This is a physically demanding and intellectually challenging role and represents an excellent opportunity to learn and develop a comprehensive range of clinical and scientific skills. Development will incorporate all elements of working in a clinical environment including QC and Scheduling and will lead to progression along a clinically specialised career path. Application If you are interested in the role, please register your details, including a copy of your CV. Please note, while we try to respond to every candidate, the high volume of applications anticipated may make this impossible and we ask for your patience and understanding. If you have not heard from us within two weeks of making your application, please assume that you have not been successful on this occasion.

Full job record

Job IDe54fb986a80792f463485f231680b20772a14e69
Org IDcced26e9-533b-4e84-adbb-2a9a93769938
Source ID2015ec9c-642c-4c8a-beff-a51e3acad478
Board ID2015ec9c-642c-4c8a-beff-a51e3acad478
Providerbamboohr
Provider Job Key480
TitleClinical Trials Associate - Japanese Speaking
Normalized Title
Statusactive
Activeyes
Location TextLondon, Southwark, SE1 1YR, United Kingdom
DepartmentClinical Operations
Team
Employment Typecontract
Workplace Type
Remote Policy
Country
RegionSouthwark
CityLondon
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://richmondpharm.bamboohr.com/careers/480
Apply URLhttps://richmondpharm.bamboohr.com/careers/480
First Seen At2026-05-30 05:44:10Z
Last Seen At2026-06-06 10:31:30Z
Last Checked At2026-06-06 10:31:30Z
Last Changed At2026-05-30 05:44:10Z
Inactive At
Source Posted At2026-02-18 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=bamboohr/board=richmondpharm/date=2026-06-06/2026-06-06T10-31-28-488Z-f421df6ac5fc6b3732925e74c12c598616bded6a8a3800262387c49514b985a4.json
Event Fields
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Parsed Structured
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Extensions
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Native Structured
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    "description": "<p><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Title: Clinical Trials Associate - Japanese Speaking</span><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Location: London Bridge, London</span><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Term: 12-month FTC, Full Time</span><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Salary: £27,000 + Benefits (Private Medical, Private Dental, Pension, 25 days Annual leave plus bank holidays &amp; many more)</span></p>\n<p><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Richmond Pharmacology are an early phase Clinical Research Organisation (CRO), where we are conducting pioneering early phase healthy participants and patient participant trials. Our experienced and world-renowned team, our central London location and our global reach contribute to making Richmond Pharmacology an exciting and dynamic place to work.</span></p>\n<p><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">A new opportunity has opened at Richmond Pharmacology for a Clinical Trials Associate to join a specialised team providing clinical support to Research Physicians and volunteers taking part in the trials of innovative new therapies. This is an entry level role with a career path focused on development of clinical excellence in the delivery of a variety of Phase I-III clinical trials.</span></p>\n<p><br><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">Key tasks will include specific clinical procedures, ward rounds, ward maintenance, volunteer support and document management. Full training will be provided and candidates will be expected to pass assessments for key skills and maintain these to a high standard throughout.</span></p>\n<p><br><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Requirements<br></span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Previous experience working as a Healthcare Assistant</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Excellent communication skills and an engaging manner</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">High energy, proactive and enthusiastic</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">High attention to detail</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Available to work shifts (early, standard, late, night) including occasional weekends</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Customer service or hospitality sector experience would be attractive</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Successful candidates will need to pass DBS checks</span><br></li>\n</ul>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt; font-weight: bold\">Key Tasks<br></span></p>\n<ul>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Clinical - phlebotomy, ECG, vitals etc - training in all procedures provided</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Documentation - study specific documents, from point of collection to quality checking</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Sample collection - efficient, safe collection of samples from volunteers including accurate labelling and management</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Volunteer support - looking after the needs and monitoring the safety of volunteers within the ward environment – Immediate Life Support (ILS) training provided</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Ward maintenance - ensuring the wards are clean, tidy and properly stocked for the care of volunteers</span></li>\n<li><span style=\"font-family: Inter, sans-serif; font-size: 12pt\">Queries - raising queries and assisting in the resolution of queries to ensure study requirements are delivered appropriately</span><br></li>\n</ul>\n<p><br></p>\n<p><span style=\"color: rgba(0, 0, 0, 0.9); font-family: Inter, sans-serif; font-size: 12pt\">As well as working daily with volunteers, you will need to interact effectively with all other departments internally and provide an efficient service to support the delivery of clinical trials. You will need to familiarise yourself with all SOP's for working within the business, as well as all details specific to the trials you will be working on. This is a physically demanding and intellectually challenging role and represents an excellent opportunity to learn and develop a comprehensive range of clinical and scientific skills. Development will incorporate all elements of working in a clinical environment including QC and Scheduling and will lead to progression along a clinically specialised career path.</span><br><br></p>\n<p><br></p>\n<p><span style=\"font-family: Inter, sans-serif; font-size: 12pt\"><span style=\"font-weight: bold\">Application<br></span><span style=\"color: rgba(0, 0, 0, 0.9)\">If you are interested in the role, please register your details, including a copy of your CV. Please note, while we try to respond to every candidate, the high volume of applications anticipated may make this impossible and we ask for your patience and understanding. If you have not heard from us within two weeks of making your application, please assume that you have not been successful on this occasion.</span></span><br></p>",
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