18 annunci per il ruolo di communication specialist - argelato, emi (recruiting in corso)

CRA (Level II)
Thermo Fisher Scientific —Bologna, Emilia-Romagna
- Tempo pieno
- Remoto
- Gestionale
- Inglese
- Microsoft Office
2 giorni
Infrastructure Specialist (IT04)
Datalogic —Calderara di Reno, Emilia-Romagna
- 38.000 € - 45.000 € all'anno
- Gestionale
- Inglese
- Laurea triennale
Entry-Level User Support Specialist | Space Sector
Etinars —Bologna, Emilia-Romagna
- Microsoft Outlook
- Inglese
- Microsoft Office
Candidatura rapida
Junior Sales Representative (Recent Graduate / Entry Level)-Italy
Cordis —Bologna, Emilia-Romagna
- Tempo pieno
- Remoto
- Medicina
- Vendite
- Inglese
SAP Controlling Business Analyst
Datalogic —Calderara di Reno, Emilia-Romagna
- 38.000 € - 45.000 € all'anno
- Gestionale
- Inglese
- Laurea magistrale
Account Executive
WTW —Bologna, Emilia-Romagna
- Tempo pieno
- Inglese
- Microsoft Office
- Capacità di presentazione
Product Development Specialist Center Region Italy
Rijk Zwaan —Bologna, Emilia-Romagna
- Vendite
- Inglese
- Laurea triennale
Desktop Support Engineer | Space Sector
Etinars —Bologna, Emilia-Romagna
- Remoto
- Inglese
- Windows
Candidatura rapida
12 giorni
Italian-speaking Tech Support Specialist in Athens (with relocation package)
Next Job Abroad —Bologna, Emilia-Romagna
- Tempo pieno
- Inglese
- Esperienza di hotel
- Convenzioni aziendali
Candidatura rapida
Ground Segment Operations & Monitoring Specialist | Space
Etinars —Bologna, Emilia-Romagna
- Inglese
- Scripting
Candidatura rapida
IT Support Engineer - End-User & Workstation Services | Space Sector
Etinars —Bologna, Emilia-Romagna
- Remoto
- Inglese
- Windows
Candidatura rapida
14 giorni
.NET/Python Software Developer | Energy Sector
Etinars —Bologna, Emilia-Romagna
- 475 € - 500 € al giorno
- Ingegneria
- Inglese
- Laurea magistrale
Candidatura rapida
IT Service Management Support Engineer | Space
Etinars —Bologna, Emilia-Romagna
- Gestionale
- Inglese
- Competenze analitiche
Candidatura rapida
Junior Talent Acquisition Specialist - Cat. protetta L.68/99
CRIF —Bologna, Emilia-Romagna
- Remoto
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
IT Support Engineer – End-User & Infrastructure Services
Etinars —Bologna, Emilia-Romagna
- Tempo pieno
- Inglese
- Windows
- Microsoft Office
Candidatura rapida
Personal Assistant - Categorie Protette art.18 L.68/99
Etinars —Bologna, Emilia-Romagna
- Tempo pieno
- Inglese
- Microsoft Office
- IT
Financial Accountant (SAP/ERP) | European Space & Defence Programmes
Etinars —Bologna, Emilia-Romagna
- Microsoft Excel
- Sistemi ERP
- Inglese
Candidatura rapida
STEM Graduate – Junior System Administrator Linux (Fixed-Term | On-site)
Etinars —Bologna, Emilia-Romagna
- Tempo pieno
- Inglese
- Laurea magistrale
- Database
Candidatura rapida

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CRA (Level II)

Thermo Fisher Scientific -
Bologna, Emilia-Romagna

Candidati adesso

Dettagli della posizione

Tempo pieno
2 giorni fa

Qualifiche

Gestionale
Inglese
Microsoft Office
Laurea magistrale
Capacità di presentazione
Terminologia medica
Time management

Descrizione completa della posizione

Work Schedule

Standard (Mon-Fri)

Environmental Conditions

Office

Job Description

Join Us as a Clinical Research Associate (Level II) – Make an Impact at the Forefront of Innovation
We have successfully supported the top 50 pharmaceutical companies and more than 750 biotechs, spanning 2,700 clinical trials across 100+ countries in the last 5 years.

As part of our global team, you’ll have the opportunity to perform and coordinate all aspects of the clinical monitoring and site management process. As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments. Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability. You will ensure audit readiness and develop collaborative relationships with investigational sites. Detailed tasks and responsibilities assigned to your role are outlined in the task matrix.

What You’ll Do:

Monitors investigator sites with a risk-based monitoring approach applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site and remote monitoring activities. Assess investigational product through physical inventory and records review. Documents observations in reports and letters in a timely manner using approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner. Conducts monitoring tasks in accordance with the approved monitoring plan. Participates in the investigator payment process. Ensures a shared responsibility with other project team members on issues/findings resolution. Investigates and follows-up on findings as applicable.

Participates in investigator meetings as necessary. Identifies potential investigators in collaboration with the client company to ensure the acceptability of qualified investigative sites. Initiates clinical trial sites according to the relevant procedures to ensure compliance with the protocol and regulatory and ICH GCP obligations, making recommendations where warranted. Performs trial close out and retrieval of trial materials.
Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications.
Provides trial status tracking and progress update reports to the Clinical Team Manager (CTM) as required. Ensures study systems are updated per agreed study conventions (e.g. Clinical Trial Management System).
Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.
Responds to company, client and applicable regulatory requirements/audits/inspections.
Maintains & completes administrative tasks such as expense reports and timesheets in a timely manner.
Contributes to the project team by assisting in preparation of project publications/tools and sharing ideas/suggestions with team members.
Contributes to other project work and initiatives for process improvement, as required.

Education and Experience Requirements:

Master degree in a life science related field or equivalent and relevant formal academic / vocational qualification.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 1 years as a clinical research monitor).
Valid driver's license where applicable.

Knowledge, Skills and Abilities:

Proven clinical monitoring skills
Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
Demonstrated ability to attain and maintain a working knowledge of ICH GCPs, applicable regulations and procedural documents
Well-developed critical thinking skills, including but not limited to critical mindset, in-depth investigation for appropriate root cause analysis and problem solving
Ability to manage Risk Based Monitoring concepts and processes
Good oral and written communication skills, with the ability to communicate effectively with medical personnel
Ability to maintain customer focus through the utilization of good listening skills, attention to detail and the ability to perceive customers’ underlying issues
Good organizational and time management skills
Effective interpersonal skills
Attention to detail
Ability to remain flexible and adaptable in a wide range of scenarios
Ability to work in a team or independently as required
Good computer skills: solid knowledge of Microsoft Office and the ability to learn appropriate software
Good English language and grammar skills
Good presentation skills

Working Conditions and Environment:

Work is performed in an office/clinical/and/or home office environment with exposure to electrical office equipment.
Frequent drives to site locations. May also include some overnight stays.

Candidati adesso

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communication specialist offerte - argelato, emi

CRA (Level II)

Infrastructure Specialist (IT04)

Entry-Level User Support Specialist | Space Sector

Junior Sales Representative (Recent Graduate / Entry Level)-Italy

SAP Controlling Business Analyst

Account Executive

Product Development Specialist Center Region Italy

Desktop Support Engineer | Space Sector

Italian-speaking Tech Support Specialist in Athens (with relocation package)

Ground Segment Operations & Monitoring Specialist | Space

IT Support Engineer - End-User & Workstation Services | Space Sector

.NET/Python Software Developer | Energy Sector

IT Service Management Support Engineer | Space

Junior Talent Acquisition Specialist - Cat. protetta L.68/99

IT Support Engineer – End-User & Infrastructure Services

Personal Assistant - Categorie Protette art.18 L.68/99

Financial Accountant (SAP/ERP) | European Space & Defence Programmes

STEM Graduate – Junior System Administrator Linux (Fixed-Term | On-site)

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