Enablement Specialist – Medical Evidence – Warsaw, Poland
Do you want to be part of an award-winning clinical research organisation who is positively working towards improving the health and lives of millions?
Clintec have an excellent career opportunity for a determined and motivated Warsaw based Enablement Specialist who strives for excellence to join our team on a full time and permanent basis, working from our sponsor’s impressive and modern office in Warsaw.
As part of the Medical Evidence Enablement Team, the Enablement Specialist plays a key role in supporting the implementation of business processes, tools and technology platforms to enable evidence delivery within BioPharmaceuticals and Oncology Medical Evidence and Regional and Local Market evidence teams.
The Enablement Specialist has the unique opportunity to collaborate and build relationships with global and local market evidence delivery teams and will work closely with internal IT/enablement partners, external vendors, and service support teams to drive continuous process improvement, resolve operational issues, and provide maintenance and business acceptance testing support for Medical Evidence owned technology platforms, enterprise interfaces and tools.
Tools and technology platforms supported by this role include, but are not limited to, Evidence Connect, Veeva CTMS and eTMF, SharePoint Online and macro-enabled excel tools.
AS AN ENABLEMENT SPECIALIST YOU WILL:
Act as a subject matter expert on Medical Evidence tools and technology platforms
Act as the lead of the CTMS change control board and drive the analysis of the effect of Externally Sponsored Research system enhancements/changes on technology platforms.
Communicate upcoming system enhancements/changes and anticipated timelines to key stakeholders.
Participate in business acceptance testing for enhancements or changes to Medical Evidence technology platforms and tools
Provide business support for issue identification and resolution in Medical Evidence owned technology platforms and tools
Coordinate and deliver awareness/training sessions for Medical Evidence owned technology platforms to Global and Local evidence delivery teams
Provide operational support to evidence delivery teams as needed
Escalate and manage issues to resolution
Bachelors degree in business or technology relevant discipline
Excellent communication (verbal and written) and collaboration skills in English language
High level awareness of the overall pharmaceutical product development process, including stages of development and functional area
Exposure to IS/IT service support & deployment with focus on issue analysis or testing
Strong proficiency in key Microsoft Office programs (e.g., Word, PowerPoint, Excel, etc.)
WHAT CAN WE OFFER YOU?
At Clintec, we believe our people are our greatest asset and understand that the best performance comes from individuals who know they are part of a valued team. You can expect to receive expert training and guidance throughout your career with us, with the opportunity to develop, progress and travel globally.
We can offer you:
A competitive salary and benefits package including private health care, holiday allowance, sports programme and Christmas vouchers
Opportunity to work with a global pharmaceutical leader in a role fully dedicated to a single sponsor
Opportunity to work on ground-breaking, challenging studies in various therapeutic areas within a stunning, state of the art office environment in Warsaw
Real career development opportunities within a friendly and social team where you can truly shine and make an impact
Clintec (an IQVIA company), established for 22 years, is an award-winning, full-service global clinical research organisation. Our head quarter office is based in Scotland, UK and we have operations across 50+ countries worldwide.
We differ from other players in the clinical research industry as we combine the agility and flexibility typical of smaller CROs with the global coverage and management associated with large CROs.
We provide clinical research support services to clients in the pharmaceutical, biotechnology and medical device industries, assisting with key product development and managing clinical trials across all major therapeutic areas, with expertise in Oncology and Rare Disease studies.
To be considered for this role, please click the APPLY NOW button. Alternatively if you want to know more about job opportunities at Clintec or our company, please visit our website www.clintec.com or contact our internal recruitment team directly at firstname.lastname@example.org.
Clinical Research / Clinical Trials / CTMS / Enablement Specialist / Medical Evidence Pharmaceutical