Study Coordinator for Cancer Clinical Trials

**Reference: 341_SS_VN**
**IDIBELL is looking for a **Study Coordinator for Cancer Clinical Trials**

**About the research group**

ICO-L’Hospitalet is a reference hospital for the clinical research in cancer. Their two units (UIC and UFF1) have been participating in 545 clinical trials with active recruitment or with current activities during 2021 and 676 patients decided to participate in them. Many of these trials are testing the most promising therapies in cancer and investigators involved in them are specialized and up-to-date with the latest advances in new treatments. UIC and UFF1 units they are the best professionals who carry out the most demanding clinical trials

**About the role**
- Coordination of Oncology Clinical Trials ( Solid Tumour neoplasms or Haematology Diseases ) into Functional Phase I Unit for early phases or Clinical Research unit for advanced phase trials.
- Support to Investigators and electronic tools implementation.
- Management of human tissues between different external referring sites.
- Administrative procedures during the study
- SAE completion
- Case Report Form training, completion and correction. Queries resolution.
- Communication with Sponsors and CROs.
- Preparation and attention to monitoring visits, audits and inspections, internal and external information meetings.

**Job requirements**

Professional experience
- At minimum of 6 months of experience in oncology or hematology cancer clinical trials ( as coordinator or data entry)
- Coordination or data entry in phase I, II and III cancer trials

Education and training
- Education: Bachelor degree in life Science
- Education In clinical trials and clinical research
- Education in Good Clinical Practices

Technical skills
- Office (Outlook, Excel, Word), internet, patient’s files
- Internet Browsers (Firefox, Chrome, Edge) and Patient’s Files

Soft skills
- To organize, order, and perform different activities with knowledge of their influence on the final outcome of a process. Understand the points of view of other people, give help. Ability to work under pressure.

Languages
- Good command of the English language
- Perfect command of Spanish and Catalan language
**We will value, but not required**
- Experience as Clinical trials Monitor
- Familiarity with SAP Argos Electronic Medical Record syste
- Previous experience in data management of oncology studies
- Previous experience in clinical trials (other than cancer)

**What do we offer**
- **Nº of positions: 1**:

- **Start date: as soon as posible**:

- **Contract duration: permanent linked to project**:

- **Estimated annual gross salary**: it is commensurate with qualifications and consistent with our pay ranges.
- You will be part of a **multicultural team**. We have a fun loving and friendly international work environment.
- **Flexible working schedule**:

- We know you have a life outside of work and we will work with you to make sure it's kept that way.
- Benefits of constant training are offered.
- We offer and promote diverse and inclusive conditions. Applicants are made free from any discrimination.

**Selection process**

**Data protection notice**

IDIBELL ensures that applicants’ personal data are processed as required by the EU General Data Protection Regulation (GDPR) and Spanish Law 3/2018 on Data Protection. Personal data is processed solely for the purpose of the selection procedure.

**Our institute**

IDIBELL is a research center that integrates the biomedical research of the Bellvitge University Hospital (HUB), the Catalan Institute of Oncology (ICO), and the University of Barcelona in the Bellvitge Campus (UB), and the Viladecans Hospital (HV). The research focuses of IDIBELL are cancer, neuroscience, translational medicine and regenerative medicine. Research, innovation and society are the pivots on which researchers work every day in order to improve the quality of life of citizens.

**Observations**

The 'HR Excellence in Research' award represents IDIBELL’s commitment to the implementation of Human Resources policies, which oversee the attracting and development of talent in an open, transparent, and based on personal merit, in alignment with the principles of the European Charter for Researchers and the Code of Conduct for the Recruitment Researchers (Charter and Code).

IDIBELL is committed to the principles of the Code of Conduct for the Recruitment of Researchers of the European Commission and the implementation of open, transparent and merit-based recruitment (OTMR).