Associate Clinical Research Associate

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,...

**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....

**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...

Freelance CRA Opportunity in ItalyRbw Consulting Llp are partnered with a small European CRO seeking a non-certified Freelance Clinical Research Associate to monitor two sites in Rome for an ongoing medical device study.Due to this being a Medical Device project, you do not need to be certifiedYour Role:Conduct site visits, including initiation, monitoring,...

**POSITION TITLE**: Lead Clinical Research Associate **DEPARTMENT**: Ora Europe **LOCATIONS**:Poland, Spain or 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...

**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...

Job SummaryWe are seeking a highly skilled Associate Director to join our Clinical Research team at MSD. This role will be responsible for managing a team of Clinical Research Associates (CRAs) and ensuring excellent study and site performance.Key ResponsibilitiesManage a team of 6-14 CRAs and ensure strict adherence to local regulations, company SOPs, and...

**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)...

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...

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...

POSITION TITLE: Lead Clinical Research Associate DEPARTMENT: Ora Europe LOCATIONS: Poland, Spain or 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...

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...

About ICONICON is a leading provider of outsourced development and commercialisation services to the pharmaceutical, biotechnology and medical device industries.Your New RoleWe are seeking an experienced Clinical Research Associate to join our team in a Clinical Research Associate role. As a CRA, you will be responsible for coordinating all activities for...

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...

**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...

**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...

**Opportunity for Freelance CRAs in Italy**Pharmiweb is looking for a dedicated Freelance Clinical Research Associate to join our dynamic team in Italy. As a Freelance CRA, you will play a key role in monitoring clinical trials for medical devices.**Key Responsibilities:**Monitor clinical trials for medical devicesStrong organizational and communication...

**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...

**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...

At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own It’ culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Integrity, Collaboration, Agility...