Clinical Coding Analyst

IQVIA

. Manage single and multi-service projects, ensuring quality deliverables on time, within budget and to the customer’s satisfaction.

Posted 10/31/2026full-timeRemote • MexicoMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Clinical Data Management, including coding processes and quality control, while effectively managing multiple global projects and maintaining strong communication with stakeholders. Proficient in Medical Dictionaries and data management systems, with a solid understanding of the clinical drug development process.

Highest-signal resume keywords

Clinical Data ManagementMedical Dictionary KnowledgeProject Management SkillsData Management ProcessesAdvanced English Communication

ATS Keywords

Tailor your resume

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills

Coding ReconciliationQuality Control ProceduresThesaurus ManagementMedical TerminologyPharmacology KnowledgeAnatomy KnowledgePhysiology KnowledgeData Management SystemsMedidata RaveClinical Trials Experience

Soft Skills

Customer NegotiationProblem SolvingCollaborationCommunication SkillsRelationship Management

Industry Keywords

Clinical TrialsGlobal ProjectsCoding StudiesQuality Improvement InitiativesOperating Procedures

About the role

Key responsibilities & impact

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.

Requirements

What you’ll need

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.