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82 IQVIA Biotech Jobs
Clin Process Spec 2
IQVIA Biotech
posted 4hr ago
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Flexible timing
Key skills for the job
Job Description
Role: An exciting opportunity to contribute to the development of first-in-class specialty medicines for patients in need within our healthcare division. You will be part of an established team that supports study teams across Phase I to Phase IV (both interventional and non-interventional) and Investigator Sponsored Studies, with or without CRO involvement. As a Clinical Trial Coordinator, you will oversee activities within a dedicated Center of Excellence, ensuring the operational success of clinical studies while collaborating with multiple cross-functional teams and CROs.
Responsibilities:
- Collaborate closely with clinical teams, offering support and specialized knowledge to ensure the successful and timely execution of clinical studies, while leveraging insights from senior leadership.
- Oversee and perform updates to the Clinical Trial Management System (CTMS) and associated databases, ensuring data integrity and compliance.
- Generate comprehensive reports, graphs, dashboards, newsletters, and data models to facilitate team meetings and enhance the decision-making process.
- Analyze diverse data sets, identify emerging data types, and synthesize information into actionable metrics and insights.
- Monitor data quality, proactively identify inconsistencies and risks, and implement corrective actions.
- Manage system access and ensure appropriate oversight of study resources, optimizing resource allocation and usage.
- Assisting and mentoring junior staff
Qualifications:
- Graduate background (e.g. Bachelor s degree) in scientific field plus substantial relevant professional experience (5 years or more in Clinical Development or equivalent) and very good knowledge and experience in own discipline and beyond
- Exceptional oral and written communication skills in English.
- Proven ability to thrive in an international, multicultural, and cross-functional matrix environment.
- Strong understanding of Clinical Operations policies and procedures, as well as ICH-GCP guidelines.
- Proficient in utilizing CTMS across all functionalities, ideally as a CTMS Super User.
- Highly experienced in generating reports from various IT systems, such as CTMS and Spotfire.
- Capable of effectively collecting and analyzing large-scale data sets from various sources for reporting purposes.
- Excellent qualitative and quantitative analytical skills.
- Ability to streamline and automate processes for increased efficiency.
- Proficient in computer skills, including advanced knowledge of MS Office (Word , PowerPoint ), Outlook, and TEAMS.
- Highly experienced in Excel , including Text, Date Time, Lookup Reference, Statistical Functions, and Pivot Tables.
- Strong administrative, coordination, and problem-solving abilities.
- Excellent time management and prioritization skills, with the capacity to work independently and efficiently under pressure.
. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com
Employment Type: Full Time, Permanent
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based on 21 employees
Flexible timing
Monday to Friday
No travel
Day Shift
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