Clinical Research Associate

3 mesi fa


Roma, Italia MSD A tempo pieno

**Job Description**:
The role 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, policies and procedures, quality standards and
adverse event reporting requirements internally and externally.
Acts as primary site contact and site manager throughout all phases of a clinical research study,
taking overall responsibility of allocated sites.
Actively develops and expands the territory for clinical research, finding and developing new
sites.
Participates in internal meetings and workstreams as SME for monitoring processes and
systems.

**Search Firm Representatives Please Read Carefully**

**Employee Status**:
Regular

**Relocation**:
**VISA Sponsorship**:
**Travel Requirements**:
**Flexible Work Arrangements**:
**Shift**:
**Valid Driving License**:
**Hazardous Material(s)**:
**Requisition ID**:R252377



  • 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....


  • Roma, Italia MSD A tempo pieno

    The role of **Associate Clinical Research Associate** support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. Under the oversight of the CRA manager the person ensures compliance of study conduct with ICH/GCP and country regulations,...


  • Roma, Lazio, Italia Tn Italy A tempo pieno

    Job Summary:Tn Italy is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with study protocols, regulations, and timelines.Key Responsibilities:Conduct site qualification, initiation, monitoring, and closeout visits...


  • Roma, Lazio, Italia Tn Italy A tempo pieno

    Job Summary:Tn Italy is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for monitoring and managing clinical trials, ensuring compliance with study protocols, regulations, and timelines.Key Responsibilities:Conduct site qualification, initiation, monitoring, and closeout visits...


  • Roma, Lazio, Italia Indiana Biosciences Research Institute A tempo pieno

    About the RoleWe are seeking a highly skilled Clinical Research Associate to join our team at Indiana Biosciences Research Institute. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials, ensuring that they are conducted in accordance with Good Clinical Practice (GCP) and regulatory requirements.Key...


  • Roma, Italia MSD A tempo pieno

    **Secondary** Language(s) Job Description**: We are looking for an **Ass. Clinical Research Associate** to join our Clinical Research Monitor Team. With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. **Responsibilities...


  • Roma, Italia Ora A tempo pieno

    **POSITION TITLE**: Clinical Research Associate I **DEPARTMENT **:Ora Europe **LOCATION**: Italy **_ Ora Values the Daily Practice of_** - Prioritizing Kindness - Operational Excellence - Cultivating Joy - Scientific Rigor_ - _______________________________________ **The Role**: Ora's Clinical Research Associate I (CRA I) develops strong clinical site...


  • Roma, Italia TFS HealthScience A tempo pieno

    **CRA Italy - 0.2/0.4 FTE - FREELANCE** **About this role** TFS HealthScience is a leading global, mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. Our expertise includes full service-capabilities, resourcing and functional service (FSP)...


  • Roma, Lazio, Italia Thermo Fisher Scientific A tempo pieno

    Job Summary:We are seeking a highly skilled Clinical Research Associate to join our team at Thermo Fisher Scientific. As a Clinical Research Associate, you will be responsible for ensuring the integrity and quality of clinical trials.Key Responsibilities:Conduct on-site visits to monitor clinical trials and ensure compliance with regulatory...


  • Roma, Italia Meditrial Europe Ltd. A tempo pieno

    Meditrial is a full-service digital research organization with a foundation in clinical trial research, education, regulatory and market access. Meditrial has been leading the medical tech industry by delivering unparalleled outcomes for innovators. Our successful track record supporting medical device and biotechnology companies in all phases of clinical...


  • Roma, Italia Cmed A tempo pieno

    The Aixial Group is an International Contract Research Organization (CRO), a member of the ALTEN Group, providing complex services in clinical trials (phase I-IV) and non-interventional studies. Our offices are located in France, UK, US, Belgium, Czech Republic, Switzerland, Denmark, Romania, and India. The CRO occupies a unique position in the clinical...


  • 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...


  • Roma, Italia ABBVIE A tempo pieno

    For our Commercial offices, based in Rome, we are looking for a Clinical Research Associate II, with following responsibilities: - Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations,...


  • Roma, Italia MSD A tempo pieno

    Job DescriptionCurrent Employees apply HERECurrent Contingent Workers apply HERESecondary Language(s) Job Description:We are looking for an Ass. Clinical Research Associate to join our Clinical Research Monitor Team.With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study,...


  • 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...


  • Roma, Italia ABBVIE A tempo pieno

    **Key responsibilities**: - Monitors activities conducted by clinical investigative sites as they relate to AbbVie clinical studies to ensure successful execution of the protocol. Ensures adherence to federal regulations and applicable local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), Monitoring...


  • Roma, Italia MSD A tempo pieno

    **Job Description**: With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site...


  • Roma, Italia MSD A tempo pieno

    With support of SrCRA/CRA and/or CRA Manager, acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites. - Develops strong site relationships and ensures continuity of site relationships through all phases of the trial. - Performs clinical study site management/monitoring...


  • Roma, Italia Sitero LLC A tempo pieno

    Sitero is an emerging leader in Clinical services and software solutions for the life sciences industry. We have experience and expertise in a diverse range of therapeutic areas and focus on innovative, technology-enabled solutions that allow our clients to focus on their core strengths. For early phase studies through Phase III clinical trials, our...


  • Roma, Italia MSD A tempo pieno

    We aspire to be the premier research-intensive biopharmaceutical company in the world. We demonstrate our commitment to patients and population health by increasing access to health care through far-reaching policies, programs and partnerships. Today, we continue to be at the forefront of research to prevent and treat diseases that threaten people and...