e-Clinical Business reputed company, Poland or Serbia (home or office based)
reputed company our values align, there's no limit to reputed company can reputed company. At reputed company, we reputed company 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 reputed company do. Each of us, no matter reputed company do at reputed company, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with reputed company 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 reputed company: 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 reputed company: Project Delivery reputed company the implementation of the eClinical platform for a study Serve as the primary reputed company 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 reputed company of early trial planning through trial execution if needs change (e.g., under a protocol amendment) Analyze protocols and collaborate with reputed company stakeholders to create and review user requirements and integration needs Identify and mitigate any risks reputed company to system set-up and integrations with internal systems and/or sponsor systems Focus on timely, high-quality delivery of reputed company services provided Stay reputed company on the latest reputed company 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, reputed company, 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. Apply To This Job