PROCESS NOW CLOSED. Deadline for submission of applications: 15/12/2017 Reference: 15/2017 Number of vacancies: 1 Offer description: S’incorporarà, a jornada completa, al VHIO…
JOBS
The fellow needs to be board certified for medical oncology. The main focus of the Molecular Therapy Research Unit (Unitat de Investigació en Teràpia Molecular, UITM) is Early Drug Development of targeted therapies so this subject should be of special interest to the fellow. Prior experience in Clinical Research will be an added value. Since the fellow will deal with patients treated in Phase I trials, the ability to communicate in Spanish is necessary for the fellowship. English is needed for communication with sponsor and investigators.
Selection of candidates
· Interview
· Curriculum vitae
· Letter of motivation
· References.
The candidates should send the application to RRHH (rrhh@vhio.net).
An organized and team-oriented individual. The ideal candidate will be in charge of processing human blood and tissue samples derived from cancer patients, which is central to our group’s work. Previous experience culturing cell lines and processing and cryopreserving blood and tissue samples will be favorably considered, but are not essential. Flexibility in working schedule is required to allow processing of unexpected samples as well as samples that arrive late in the afternoon. Both full-time as well as part-time working schedule can be considered to allow for this flexibility.
Application:
Potential candidates should submit a curriculum vitae and letter of intent via email addressed to Alena Gros: rrhh@vhio.net
Review of applications will commence immediately.
Applicants must have a BSc and at least 2 years of experience in molecular biology techniques and animal experimentation.
Experience working in stem cells and cancer mouse models will be favourably considered.
Salary will be based on the specific profile and experience of the candidate.
If you are interested, please send a letter of intent, your CV and references to: mabad@vhio.net.
Buscamos una persona con:
– Estudios en biología, farmacia, enfermería o ciencias relacionadas con la salud.
– Conocimientos y experiencia en la gestión y monitorización de ensayos clínicos.
– Imprescindible buen nivel de inglés (Advance o superior).
– Imprescindible dominio de herramientas ofimáticas.
– El perfil del candidato será el de una persona con capacidad de organización, coordinación y trabajo en equipo.
– También será imprescindible la acreditación previa en ensayos clínicos, se valorará Máster en Monitorización de ensayos clínicos.
– Disponibilidad para viajar.
Requisits:
Busquem una persona amb:
– estudis en biologia, farmàcia, ,infermeria o ciències relacionades amb la salut
– coneixements sobre gestió d’assaigs clínics
– es valorarà experiència en assaigs clínics a nivell hospitalari
– es valorarà experiència en gestió de personal
– es valorarà acreditació en bones pràctiques clíniques
– imprescindible bon nivell d’anglès (Advanced o superior)
– imprescindible domini d’eines ofimàtiques
El perfil del candidat serà el d’una persona amb capacitat d’organització, coordinació, supervisió i treball en equip. Es essencial pel rol, la possessió d’excel·lents habilitats interpersonals i capacitat de lideratge.
També serà imprescindible l’acreditació d’experiència prèvia en assaigs clínics.
Es tracta d’un lloc de treball dins d’un grup dinàmic i ambiciós amb gran projecció.
We seek
A Quality Assurance Technician with experience in clinical trials, preferably a Bachelor´s degree, knowledge of GCP (Good Clinical Practice), experience in quality inspection, auditing and testing as well as implementing corrective action programs. The successful candidate will also have excellent computer skills (Microsoft Office and databases), knowledge of QA tools, concepts, methodologies and relevant regulatory requirements.
Key Competencies
The following competencies will also be favorably considered:
• Attention to detail
• Good verbal and written communicator
• Data collection and management
• Excellent analytical skills with the ability to problem solve and take decisions
• Good planning and organizational skills
• Customer service orientated
• Team player
Main Roles and Responsibilities
Draft quality assurance policies and procedures
Interpretation and implementation of quality assurance standards
Evaluate adequacy of quality assurance standards
Devise sampling procedures and indications for recording and reporting quality data
Review the implementation and efficiency of quality and inspection systems
Plan, conduct and monitor testing and inspection of materials and products to ensure finished product quality
Document internal audits and other quality assurance activities
Investigate customer complaints and non-conformance issues
Collect and compile statistical quality data
Analyze data to identify areas for improvement in the quality system
Develop, recommend and monitor corrective and preventive actions
Prepare reports to communicate outcomes of quality activities
Identify training needs and organize training interventions to meet quality standards
Coordinate and support on-site audits conducted by external providers
Evaluate audit findings and implement appropriate corrective actions
Monitor risk management activities
Manage document management systems
Guarantee ongoing compliance with quality and industry regulatory requirements
Applicants must have a PhD, BSc or MSc with at least 2 years relevant laboratory experience in molecular biology techniques. Experience in genomics will be favorably considered. Fluency in English and computer literacy are imperative.
Busquem candidat amb:
- Nivell d’estudis universitaris.
- Capacitat de donar suport adient, eficient i precís.
- Coneixements d’equipaments existents a centres de recerca.
- Formació específica en aquests tipus d’intal·lacions i normatives (Prevenció de Riscos Laborals).
- Usuari/a avançat d’eines ofimàtiques.
- Domini del castellà, català i anglès tant parlat com escrit.
- Estudios superiores – licenciado/a en ciencias relacionadas con la salud.
- Imprescindible dominio de herramientas informáticas como Excel y experiencia con bases de datos.
- Se valorará experiencia profesional en investigación clínica o preclínica.
- Se valorará conocimiento de estadísticas y en programación ( análisis de datos como programa R).
- Dominio del castellano y catalán tanto hablado como escrito y buen nivel de inglés
