Clinical Research Associate(Remote Monitoring)

**Clinical Research Associate( Work from Home)**

**About the company**:
**We **provide enterprise grade platforms that accelerates adoption of Kubernetes and Data.

Gravity, our flagship platform, provides a simplified Kubernetes experience for developers by removing all the removing all the underlying complexities. Developers can use tailor-made workflows to deploy their Microservices, Workers, Data and MLOps workloads to Kubernetes environments across multiple Cloud Providers. Gravity takes care of all the Kubernetes related orchestration such as cluster provisioning, workload deployments, configuration and secret management, scaling and provisioning of cloud services. Gravity also provides out of the box Observability for workloads helping developers to get started with Day 2 operations quickly.

Dark Matter provides a unified data platform for enterprises to extract value out of their data lakes. Data Data Engineers and Data Analysts can discover datasets in enterprise data lakes through an Augmented Data Catalog. Data Profile, Data Quality & Data Privacy are deeply integrated within the catalog to provide an immediate snapshot of datasets in Data Lakes. Organizations can maintain Data Quality by defining quality rules that automatically monitor Accuracy, Validity and Consistency of data to meet their data governance standards. The built-in Data Privacy engine can discover sensitive data in your data lakes and can take automated actions (such as redactions) through an integrated Policy and Governance engine

**Roles and Responsibilities**

**Remote monitoring**:Remote monitoring: CRAs need to master remote monitoring techniques and understand electronic data capture systems.

**Virtual engagement**:CRAs need to be able to engage with patients virtually **.**

**Data integrity**:CRAs need to ensure data integrity and compliance remotely, which requires a deep understanding of digital platforms and problem-solving skills.

**Communication**: CRAs need to have heightened communication skills.

**Adaptability**:CRAs need to be adaptable.

**Site processes**:CRAs act as site processes specialists, ensuring that the trial is conducted according to the approved protocol, guidelines, regulations, and SOPs.

**Study progress**:CRAs review study progress, including the quality and accuracy of data collection, compliance of patients to trial visits and assessments, and investigational product accountability.

**Clinical practices**:CRAs ensure good clinical practices are maintained throughout the trial and offer direction when need **ed.**

**Audit readiness**:CRAs ensure audit readiness.

**Virtual engagement**:CRAs need to be able to engage with patients virtually.

**Data integrity**:CRAs need to ensure data integrity and compliance remotely, which requires a deep understanding of digital platforms and problem-solving skills.

**Communication**:CRAs need to have heightened communication skills.

**Adaptability**:CRAs need to be adaptable.

**Site processes**:CRAs act as site processes specialists, ensuring that the trial is conducted according to the approved protocol, guidelines, regulations, and SOPs.

**Study progress**:CRAs review study progress, including the quality and accuracy of data collection, compliance of patients to trial visits and assessments, and investigational product accountability.

**Clinical practices**:CRAs ensure good clinical practices are maintained throughout the trial and offer direction when needed.

**Audit readiness**:CRAs ensure audit readiness

**Requirements and Skills**
- Hold a Master's/bachelor's degree in Pharma, Science/ Computer Science, Information Systems, or a related field
- Have 3 to 8 years of work experience as Clinical Research Associate or similar CMS domain development role.
- Problem-solving attitude
- Team Sprit