DATA ENTRY :
Details :
Company : IBIMA Plataforma BIONAND
Field : Medical sciences / Cancer research
Country : Spain
Deadline : 29 Sep 2023 – 2:00 PM
Contract : Permanent
Job Status : Full-time
Per Week : 35 Hours
Description :
Collaborate In Research: Clinical-translational research in breast, prostate, gynaecological, digestive and germ cell cancers.
Job description :
- Collecting and entering data into various patient records and Case Report Forms (CRFs) for clinical trials.
- Prepare for monitoring visits and actively participate in them alongside the monitor as and when required.
- Familiarizing with the protocols of the different clinical trials conducted in the Medical Oncology Service.
- Understanding the testing schedule for each trial and the specific procedures required for each study
- Ensuring compliance with the protocols, as well as adhering to the Standards of Good Clinical Practice and relevant legislation, is of utmost importance
- Responsible for resolving any discrepancies or queries that arise during the data collection process.
- Responsible for handling the situation and ensuring that the data is properly managed and restored once the system is back online.
- Timely reporting of Serious Adverse Events to the promoter within 24 hours is a critical aspect of the role.
- Attending Investigator Meetings is an integral part of the responsibilities, as it allows you to stay updated on the progress and requirements of the trials.
- Managing the testing schedule for assigned protocols is another crucial aspect of the work. This involves coordinating activities related to pharmacokinetics, pharmacodynamics, genomics, radiological procedures, and patient monitoring.
- Updating the database with information regarding the number of trials conducted in the Medical Oncology Service and the corresponding number of patients enrolled in each trial.
Requirements :
- Data Entry experience (0.5 points per year worked, up to 2 points)
- Oncology experience (0.5 points per year worked, up to 1 point)
- Administrative, methodological, and computer knowledge (1 point – 0.5 points per course)
- Possession of updated GCPS and IATA certificates (1 point – 0.5 points per course)
- Experience in managing clinical trial platforms such as Inform, Rave, Chiphone, IXRS (2 points – 0.5 points per year of experience)
- These requirements should be validated with a certificate from a reputable organization or a declaration of competence.
Apply :
Send Via Mail to : ope@ibima.eu
