Clinical Research Associate I

6 giorni fa

Roma, Italia Labcorp A tempo pieno

**Responsibilities include**:

- All details of site management as prescribed in the project plans
- Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks
- Negotiation of study budgets with potential investigators and cooperation with Labcorp Drug Development legal department with statements of agreements
- Serious Adverse Event (SAE) reporting, production of reports, narratives and follow up of SAEs.
- Case Report Forms (CRF) review; query generation and resolution against established data review guidelines on Labcorp Drug Development or client data management systems

**Requirements**:

- Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
- Excellent understanding of Serious Adverse Event (SAE) reporting
- Ability to resolve project-related problems and prioritize workload for self and team
- You have previous clinical research monitoring Experience (including pre-study, initiation, routine monitoring and closeout visits).

**Labcorp is proud to be an Equal Opportunity Employer**:
As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.

For more information about how we collect and store your personal data, please see our Privacy Statement.

  • Clinical Research Associate, Italy

    2 giorni fa

    Roma, Italia EastHORN Clinical Services A tempo pieno

    **Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....

  • Clinical Research Associate

    2 settimane fa

    Roma, Italia AL Solutions A tempo pieno

    Clinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:Oversight and...

  • Clinical Research Associate

    2 settimane fa

    Roma, Italia AL Solutions A tempo pieno

    Clinical Research Associate – International CRO – ItalyMy client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France. We're looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused.Key Responsibilities:Oversight and...

  • Clinical research associate.

    7 giorni fa

    Roma, Italia AL Solutions A tempo pieno

    Clinical Research Associate – International CRO – Italy My client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France . We're looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused. Oversight and monitoring of a single...

  • Clinical Research Associate

    2 giorni fa

    Roma, Italia AL Solutions A tempo pieno

    Clinical Research Associate – International CRO – Italy My client, an international mid-sized CRO, is seeking an experienced CRA to support and take responsibility for a Phase 3 study in France . We’re looking for someone who works confidently on their own, shows strong proactivity, and is highly quality focused. Key Responsibilities: Oversight and...

  • Lead Clinical Research Associate

    16 ore fa

    Roma, Italia Ora A tempo pieno

    **POSITION TITLE**: Lead Clinical Research Associate **DEPARTMENT**: Ora Europe **LOCATIONS**:Remote, Italy **Ora Values the Daily Practice of ** - Prioritizing Kindness - Operational Excellence - Cultivating Joy - Scientific Rigor_ At Ora, we are building the future of ophthalmic clinical research. As the world's leading full-service ophthalmic drug and...

  • Clinical Research Associate

    7 giorni fa

    Roma, Italia The BIG Jobsite A tempo pieno

    The Clinical Research Associate position at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with a medical and/or health/life science background who want to explore the research field and be part of a team bringing...

  • Clinical Research Associate

    2 settimane fa

    Roma, Italia TFS HealthScience A tempo pieno

    Overview: TFS HealthScience is excited to be expanding our **Strategic Resourcing Solutions (SRS) **team and we are looking for an experienced, highly motivated **Clinical Research Associate** who shares our vision of providing clinical research excellence. Our SRS team is a highly experienced international group of professionals led by an industry...

  • Position: Clinical Research Associate

    4 giorni fa

    Provincia di Roma, Lazio, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is a full-service clinical research organization (CRO) dedicated to clinical trial conduct, medical education, regulatory affairs and market access. Our offices are located in Germany, Italy, Switzerland, UK, United States and our teams rely on digital tools to work collaboratively to achieve shared goals. Since 2008, Meditrial delivers...

  • Clinical Research Associate

    6 giorni fa

    Roma, Italia MSD A tempo pieno

    The role of Clinical Research Associate is accountable for performance and compliance for assigned protocols and sites in a country. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations, our Company policies and procedures, quality standards and adverse event reporting requirements...