The Source department of Chiltern acts in a similar way to that of a staffing solutions provider. The department is currently seeking a Data Entry/Registries Associate in Poland to work for our client a leading Biotech company. Candidates will be employed through Chiltern’s Poland entity to work directly for our client. The role is working on a reduced fte.
-To enroll patients in to the applicable Registries LSD database using Electronic Data Capture (EDC) and entering information in (electronic) Case Report Forms (eCRFs)
-Data entry of medical history from patient notes in to the Registries electronic CRF’s using Electronic Data Capture (EDC) under the supervision of the Principal Investigator.
-To update eCRF’s of existing enrolled patients for all follow up assessments after initial data entry of patient’s medical history.
-To liaise with site personnel in regards to patient notes.
-To liaise with site staff to resolve data queries that arise during the CRF completion.
-To assist site staff with the maintenance of patient consent lists for the Registries and the distribution of information to potential candidates for the Registries.
-To assist site personnel with other tasks as requested and required.
•Must be fluent in Polish and a good level of English
•Would suit candidates with Data Entry or CTA experience
To apply for this position, please send your CV to email@example.com, for a confidential discussion please call Nicky Cooke on + 44 1753 216 729.
For more extensive information about Chiltern, please visit our web site at www.chiltern.com
Please note that if your experience does not mirror that of our requirements for this role you may not receive a response.
PLEASE NOTE: AGENCY OR THIRD PARTY APPLICATIONS WILL NOT BE CONSIDERED. THANK YOU.
Candidates must be eligible to work in Poland
CTA, Data Entry, Clinical Trial Administrator, Registries, Registries Associate, Poland