Manage single and multi-service projects, ensuring quality deliverables on time
Provide expert skills as part of a Clinical Data Management (CDM) team
Serve as internal or external point of contact on standalone coding studies or accounts
Maintain post-coding dictionary up-versioning synonym and coding reconciliation
Perform Dictionary up-versioning activities
Perform external verbatim coding of data from non-EDC sources
Perform comprehensive quality control procedures
Perform Serious Adverse Event (SAE) coding reconciliation activities
Collaborate with customers and develop solutions and action plans for issues
Proactively identify, solve quality issues and deliver projects as per agreed timeline
Identify and implement processes and quality improvement initiatives
Provide review and expert opinion in developing, revising, and maintaining standard operating procedures
Develop and maintain good communications and working relationships with the CDM team and client stakeholders

High School Diploma or equivalent
Pharmacy, dental, medical, nursing, life sciences or related field qualification or educational equivalent
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 in handling complex customer negotiations and bid defense meeting
Thesaurus management experience
Excellent knowledge of Medical Dictionaries used for coding (e.g. MedDRA, WHODD, ICD9, etc.)
Excellent knowledge of Medical Terminology, Pharmacology, Anatomy, and Physiology
Advanced knowledge of data management processes and systems
Excellent understanding of clinical drug development process
Good project management skills related to all phases of clinical studies
Excellent knowledge of operating procedures and work instructions
Excellent English written and oral communication skills.

Clinical Coding Analyst

Key skills