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.
This position is available in the following EMEA locations - Romania, Poland, Serbia, South Africa and we offer fully remote home based working.
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
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
A little about us:
Highly qualified and dynamic team. Multinational working environment. Smooth induction and training program. We offer competitive financial packages, training, and development. Expect exciting professional challenges but with a healthy work/life balance. We value your welfare just as highly as that of our patients.
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