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HomeCompaniesParexeleClinical Business Lead - based in Romania, Serbia, Poland, Spain, South Africa

eClinical Business Lead - based in Romania, Serbia, Poland, Spain, South Africa

Parexel · South Africa-Bloemfontein-Remote; 8 Locations; Serbia-Belgrade; Spain-Remote; Poland-Warsaw-Business Garden; Poland-Remote; Serbia-Remote; Romania-Remote; Spain-Madrid · Remote · Active · Workday Recruiting

Job facts

FieldValue
CompanyParexel
TitleeClinical Business Lead - based in Romania, Serbia, Poland, Spain, South Africa
Normalized title-
Department / team-
LocationSouth Africa
Work modelRemote / Remote
Employment type-
Salary-
Statusactive
ATS providerWorkday Recruiting
Posted / first seen2026-06-05 / 2026-06-06
Changed / last seen2026-06-06 / 2026-06-06

Related slices

PageWhat it containsOpen
Company jobsActive postings from Parexel.Open
Company breakdownsRole, location, ATS, and work model facets for this company.Open
ATS provider jobsActive postings observed through Workday Recruiting.Open
Provider filtered searchThe same provider as a filtered job collection.Open
Work model jobsActive Remote 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

CompanyParexel
Sourcea38f5933-8d87-4b90-bb56-84b4c1881427
ATS providerWorkday Recruiting

Description

When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. The role can be fully home based in Romania, Serbia, Poland, Spain, South Africa Picture Yourself At Parexel: The role leads the implementation of technology at a clinical trial’s outset, ensuring timely start-up, quality delivery, and compliance with the study protocol and client contracted services. The individual has responsibility for the design, requirements gathering, requirements documentation, and configuration. What You'll Do At Parexel: Project Delivery Lead the implementation of the eClinical platform for a study Serve as the primary point of contact internally and with external customers as needed regarding study technology, data integrations, and requirements Collaborate with Project Leaders, Project Specialists, and other study team members on study technology needs from the point of early trial planning through trial execution if needs change (e.g., under a protocol amendment) Analyze protocols and collaborate with all stakeholders to create and review user requirements and integration needs Identify and mitigate any risks related to system set-up and integrations with internal systems and/or sponsor systems Focus on timely, high-quality delivery of all services provided Stay current on the latest Parexel technology offerings, integration issues, and relevant clinical trial process developments in the industry Client Management Interact with external clients as needed for discussion on technology set-up, modifications, and integrations Demonstrate a proactive approach to providing solutions in a timely manner Here are a few requirements specific to this advertised role: Proven experience in clinical trials (CRO/Pharma) Experience in clinical trial systems (e.g., CTMS, EDMS, EDC, IVRS, reporting tools) and in configuration of these systems Global virtual team coordination experience for trial technology set-up Ability to develop detailed awareness of Clinical Research Services, external vendor software and tools with practical knowledge of how these applications work and provide efficiency to operations Knowledge of SOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application Experience or knowledge of data standards such as CDISC SDTM Strong ability to work to tight deadlines Fluent English Educated to a degree level Strong customer focus Excellent verbal and written communication skills Good project management skills In depth understanding and experience of clinical trial processes Demonstrated adeptness in learning new systems and function in an evolving technical environment

Full job record

Job IDc724715b1b8a0b4de1dbffc138927fa1de92a685
Org ID0c6955f0-4e0e-43b2-98b7-c020651fe1bc
Source IDa38f5933-8d87-4b90-bb56-84b4c1881427
Board IDa38f5933-8d87-4b90-bb56-84b4c1881427
Providerworkday
Provider Job Key/job/South-Africa-Bloemfontein-Remote/eClinical-Business-Lead---based-in-the-UK-South-Africa-or-selected-EU-locations_R0000036452
TitleeClinical Business Lead - based in Romania, Serbia, Poland, Spain, South Africa
Normalized Title
Statusactive
Activeyes
Location TextSouth Africa-Bloemfontein-Remote; 8 Locations; Serbia-Belgrade; Spain-Remote; Poland-Warsaw-Business Garden; Poland-Remote; Serbia-Remote; Romania-Remote; Spain-Madrid
Department
Team
Employment Type
Workplace Typeremote
Remote Policyremote
CountrySouth Africa
Region
City
Salary Raw
Salary Min
Salary Max
Salary Currency
Salary Period
Source URLhttps://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/South-Africa-Bloemfontein-Remote/eClinical-Business-Lead---based-in-the-UK-South-Africa-or-selected-EU-locations_R0000036452
Apply URLhttps://wd1.myworkdaysite.com/recruiting/parexel/Parexel_External_Careers/job/South-Africa-Bloemfontein-Remote/eClinical-Business-Lead---based-in-the-UK-South-Africa-or-selected-EU-locations_R0000036452
First Seen At2026-06-06 09:44:42Z
Last Seen At2026-06-06 09:44:42Z
Last Checked At2026-06-06 09:44:42Z
Last Changed At2026-06-06 09:44:42Z
Inactive At
Source Posted At2026-06-05 00:00:00Z
Source Updated At
Raw Payload Uris3://job-postings-prod-raw-590183727216/raw/provider=workday/board=wd1.myworkdaysite.com|parexel|Parexel_External_Careers/date=2026-06-06/2026-06-06T09-44-03-769Z-d8971a44a3c4aa5e8991760bf3f97217cce82940a3203cd02265c8253b6dbb66.json
Event Fields
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Parsed Structured
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Extensions
{}
Native Structured
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    "jobDescription": "<p><b>When our values align, there&#39;s no limit to what we can achieve.</b><br /> <br />At Parexel, we all share the same goal - to improve the world&#39;s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.</p><p>Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we&#39;re committed to making a difference.</p><p></p><p></p><p><u><b>The role can be fully home based in Romania, Serbia, Poland, Spain, South Africa</b></u></p><p></p><p><b>Picture Yourself At Parexel:</b></p><p></p><p>The role leads the implementation of technology at a clinical trial’s outset, ensuring timely start-up, quality delivery, and compliance with the study protocol and client contracted services. The individual has responsibility for the design, requirements gathering, requirements documentation, and configuration.</p><p></p><p><b>What You&#39;ll Do At Parexel:</b></p><p></p><p><b><i>Project Delivery</i></b></p><p></p><ul><li><p>Lead the implementation of the eClinical platform for a study</p></li><li><p>Serve as the primary point of contact internally and with external customers as needed regarding study technology, data integrations, and requirements</p></li><li><p>Collaborate with Project Leaders, Project Specialists, and other study team members on study technology needs from the point of early trial planning through trial execution if needs change (e.g., under a protocol amendment)</p></li><li><p>Analyze protocols and collaborate with all stakeholders to create and review user requirements and integration needs</p></li><li><p>Identify and mitigate any risks related to system set-up and integrations with internal systems and/or sponsor systems</p></li><li><p>Focus on timely, high-quality delivery of all services provided</p></li><li><p>Stay current on the latest Parexel technology offerings, integration issues, and relevant clinical trial process developments in the industry</p></li></ul><p></p><p><b><i>Client Management</i></b></p><p></p><ul><li><p>Interact with external clients as needed for discussion on technology set-up, modifications, and integrations</p></li><li><p>Demonstrate a proactive approach to providing solutions in a timely manner</p></li></ul><p></p><p><b>Here are a few requirements specific to this advertised role:</b></p><p></p><ul><li><p>Proven experience in clinical trials (CRO/Pharma)</p></li><li><p>Experience in clinical trial systems (e.g., CTMS, EDMS, EDC, IVRS, reporting tools) and <u>in configuration of these systems</u></p></li><li><p>Global virtual team coordination experience for trial technology set-up</p></li><li><p>Ability to develop detailed awareness of Clinical Research Services, external vendor software and tools with practical knowledge of how these applications work and provide efficiency to operations</p></li><li><p>Knowledge of SOPs/Guidelines/System Life Cycle methodologies, ICH-GCP and any other applicable local and international regulations such as 21 CFR Part 11 and proven practical application</p></li><li><p>Experience or knowledge of data standards such as CDISC SDTM</p></li><li><p>Strong ability to work to tight deadlines</p></li><li><p>Fluent English</p></li><li><p>Educated to a degree level</p></li><li><p>Strong customer focus</p></li><li><p>Excellent verbal and written communication skills</p></li><li><p>Good project management skills</p></li><li><p>In depth understanding and experience of clinical trial processes</p></li><li><p>Demonstrated adeptness in learning new systems and function in an evolving technical environment</p></li></ul>",
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