CRA
Clinical Research Associate
We’re looking for Clinical Research Associate to join our team!
The CRA will perform clinical trial monitoring activities to:
- Ensure collection of accurate clinical data within prescribed timelines
- Identify, resolve, mitigate, and escalate risks and issues
- Support clinical Investigational team
- Collaborate with thirth party vendors/CRO/Sponsor
- Take responsibility for multiple studies
- work independently with team support
- deliver monitoring reports for sponsor approval as per given timelines
- Schedule site visits for monitoring as required by study protocol
You’ll be responsible for:
- Monitoring data - remotely, on site, and via other approved models
- Planning day-to-day activities for study monitoring and setting priorities by site.
- Preparing for and conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites.
- Working with the line manager and CM to ensure that visit metrics are maintained as required.
- Gauging the quality of clinical deliverables and addressing quality issues with team members.
- Managing query resolution with study sites
- Maintaining the project tracking system of subjects and site information.
- Participating in Investigators’ Meetings
- Maintaining contact with investigator sites via telephone calls between visits.
- Ensuring adherence to study timelines and budgets.
- Identifying and escalating potential risks and identifying retraining opportunities for site study teams.
Experience and Qualifications
- Human science degree (medicine/pharmacy/biology/dental)
- Skills acquired through experience or education
- English language (spoken/written)
The CRA will perform clinical trial monitoring activities to:
- Ensure collection of accurate clinical data within prescribed timelines
- Identify, resolve, mitigate, and escalate risks and issues
- Support clinical Investigational team
- Collaborate with thirth party vendors/CRO/Sponsor
- Take responsibility for multiple studies
- work independently with team support
- deliver monitoring reports for sponsor approval as per given timelines
- Schedule site visits for monitoring as required by study protocol
You’ll be responsible for:
- Monitoring data - remotely, on site, and via other approved models
- Planning day-to-day activities for study monitoring and setting priorities by site.
- Preparing for and conducting qualification, study initiation, interim monitoring, and close-out visits at investigator sites.
- Working with the line manager and CM to ensure that visit metrics are maintained as required.
- Gauging the quality of clinical deliverables and addressing quality issues with team members.
- Managing query resolution with study sites
- Maintaining the project tracking system of subjects and site information.
- Participating in Investigators’ Meetings
- Maintaining contact with investigator sites via telephone calls between visits.
- Ensuring adherence to study timelines and budgets.
- Identifying and escalating potential risks and identifying retraining opportunities for site study teams.
Experience and Qualifications
- Human science degree (medicine/pharmacy/biology/dental)
- Skills acquired through experience or education
- English language (spoken/written)
