Centralized Monitor, Dutch Speaking, Office Based
7 months ago
**Centralized Monitor - Dutch Speaking**:
**A**re you**:
- Someone who understands dynamics of working with the sites?
- Results driven and detail-oriented?
- Good at supporting others on problem solving?
- Good at planning, time management and prioritization?
- Skilled at software and computer use, that enjoys technology applied to data analysis?
- Able to communicate efficiently and work well across cultures and geographies?
- ** Can you speak, read and write Dutch?**
If you have answered ‘yes’ to any of the above questions, you might be the Centralized Monitor that we are looking for
**What is a Centralized Monitor?**
A Centralized Monitor (CM) is a key skilled and clinically experienced team member of IQVIA Centralized Monitoring Department. A CM provides remote project support and assistance across multiple projects, sites and teams and reviews the structured clinical data output with access to medical charts.
**What are the responsibilities of a CM?**
As a CM, you will:
- Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs respective regulation and guidelines.
- Ensure accurate completion and maintenance of internal systems, databases, tracking tools/reports for the project specific information.
- May perform Management of triggers and preparation of i-site pack for respective sites and countries for assigned study(ies).
- May assist in Developing required basic data analytics scope and performing the trend analytics for their respective study(ies).
- May participate in (study) team meetings and interaction with cross functional staff to verify information and/or triage new data issues or prior identified action items
- Escalate quality issues pertaining to site to respective Centralized Monitoring Lead / Sr. Centralized Monitor.
- May perform Subject Level Data Review that require further investigation with the clinical site to determine overall accuracy.
- Review any other information as necessary to determine overall readiness of the patient information for next level review.
- Interaction with sites/CRA and follow-up on study required milestones from the project start until close out.
- You must have a Bachelor's degree in life sciences or related field
- At least 1 year experience in clinical research field preferred.
- Fluency in Afrikaans and English is essential.
- ** Must be able to speak, read and write Dutch.
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