
10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
🔥 0 minutes ago
Where this job comes from
Posted on IQVIA's careers page, not through a job board
First seen by Remote Rocketship 0 minutes ago

10,000+ employees
💼 Consulting
🏭 Manufacturing
📣 Marketing
💰 $1G Post-IPO Debt on 2023-05
Consulting • Manufacturing • Marketing
IQVIA is a global leader in data analytics and technology solutions, dedicated to improving health outcomes. The company utilizes its Connected Intelligence platform to harness the power of advanced data analytics and artificial intelligence, facilitating innovation in healthcare. IQVIA focuses on various areas, including clinical research, technology, and consulting services to solve complex healthcare challenges and accelerate the delivery of new therapies to patients.
• Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction. • Provide expert skills as part of a Clinical Data Management team to provide quality data that meet customer needs. • Serve as internal or external point of contact on standalone coding studies or accounts. • Maintain post-coding dictionary up-versioning synonym and coding reconciliation to align coding to latest dictionary versions. • Perform dictionary up-versioning activities. • Perform external verbatim coding of data from non-EDC sources in line with required coding dictionary versions. • Perform comprehensive quality control procedures. • Perform Serious Adverse Event coding reconciliation activities. • Collaborate with customers and develop solutions and action plans for issues, escalations and road blocks. • Proactively identify and solve quality issues and deliver projects as per agreed timeline. • Identify and implement processes and quality improvement initiatives in the data management and coding function. • Provide review and expert opinion in developing, revising, and maintaining standard core operating procedures and work instructions. • Develop and maintain good communications and working relationships with the Clinical Data Management team and client stakeholders.
• High School Diploma or equivalent Pharmacy, Dental, Medical, Nursing, life sciences or related field qualification or educational equivalent. • Advanced English both written and communication skills, works in a global team. • 3/4 years of relevant experience in clinical trials within a similar function. • Proven competence in managing the delivery of coding or/and other data management processes for multiple global projects. • Experience handling complex customer negotiations and bid defense meeting. • Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.). • Thesaurus management experience. • Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology. • Advanced knowledge of data management processes and systems and advanced ability to apply this knowledge in practice; Medidata Rave is preferred. • Excellent understanding of the clinical drug development process. • Good project management skills related to all phases of clinical studies. • Excellent knowledge of operating procedures and work instructions and ability to apply them in practice. • Based in Mexico.
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