Clinical Research Associate
5 days ago
We are seeking a highly skilled and experienced Centralized Monitor to join our team at IQVIA. As a Centralized Monitor, you will play a key role in ensuring the quality and integrity of clinical trials.
Key Responsibilities:- Perform centralized monitoring activities on assigned projects and evaluate the quality and integrity of the study as per the protocol, SOPs, and respective regulations 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 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.
- Evaluate and escalate quality issues pertaining to sites to respective Centralized Monitoring Lead/Sr. Centralized Monitor.
- May perform subject-level data review that requires 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.
- Bachelor's degree in life sciences or related field.
- At least 1 year of experience in clinical research field preferred.
- Fluency in Afrikaans and English is essential.
- Must be able to speak, read, and write Dutch.
IQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.
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Bloemfontein, Orange Free State, South Africa Parexel Full time{"title": "Senior Regulatory Affairs Associate", "description": "Key ResponsibilitiesAs a Senior Regulatory Affairs Associate at Parexel, you will be responsible for ensuring the timely performance of work within a project scope to the quality expectations of internal stakeholders and clients.You will bring your specialist knowledge of clinical trial...
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