Suki Dhamu Email & Phone Number

London Area, United Kingdom

London, England, United Kingdom

• Responsible for coding in MedDRA and WHO-DD of all adverse events, concomitant therapies and concomitant diagnosis in all clinical trials. • Conducted medical coding activities following company/study specific coding guidelines• Reviewed coding Reports ensuring consistency within and across projects. • Supervised the medical coding performed by External Service providers, including training, review of Coding reports and the deliverables to ensure study targets were met.• MedDRA and WHO-DD upversion was performed according to SOPs and guidance documents• Updates to the synonym tables we done on a regular basis to keep the lists up to date• Worked with Drug Safety/Pharmacovigilance to ensure consistent working practices between Clinical Coding and Safety MedDRA and WHO-DD coding. • SMQ’s, SDGs, Customised MedDRA Queries (CMQs) and Customised drug groupings (CDGs) were provided on request with guidance from Drug Safety/Pharmacovigilance.

London, England, United Kingdom

• Provide exceptional standard of service to clients and anticipate future needs to improve client relationship• Point person for assigned projects to co-ordinate coding and reviews globally• Provide expertise in set-up of the metrics collection automation and other review (e.g. coding processes and quality), including automation of a manual metrics collection process, using macro programming, thus reducing time and error rate of the manual process.• Set-up of a standard specifications for Coding Reports. Programmers were asked to standardize all the reports using the standard specification which included the formulas to help reduce review time for internal and medical reviews.• Communicating to understand complicated/unclear issues, by picking up the phone and defining the problems and resolving the issues quickly, thus reducing time spent on emails and meetings.• Key achievements• Contribute to the implementation of a Coding Automation tool – enabling efficient review of coded data• Subject Matter Expert in Coding and Upversion of projects, MedDRA /WHODrug• Increased automation - Coding Reports to reduce time and effort of reviewing. Key fields duplicated on rows highlighted, using excel formulas. A status flag added to show which term has changed, is new or unchanged (previously reviewed). • Initiate macro programming in small steps to automate the manual process during the Quality metrics review. Quality metrics are required for each study at a global level. Collection of quality metrics with a view to automation is near completion, creating a significantly reduced error rate and reduced manual time.• Output existing Metrics Inform report, identify live studies and relevant information/columns to modify to required Quality Metrics Report. Formulas applied to calculate the required quality metrics, replacing manual coding metric collection.

• Use in-depth experience of Coding skills to develop tools and process improvement to benefit the Coding Team• Perform coding/review, using MedDRA/WHODrug, other Sponsor specified dictionaries, and provide support for difficult coding• Participate in system upgrades (E.g., Upversion), UAT for Coding environment• Provide support, training, mentoring, feedback, and performance/competency input for all dictionary specialists

Maidenhead, England, United Kingdom

• Executes Data Management coding functions in accordance with Chiltern and/or Sponsor Standard Operating Procedures (SOPs), guidelines, and global standards• Maintains coding integrity and ensure consistency across all project’s Key responsibilities• Collaborates with Chiltern and Sponsor Data Management (DM), other departments to ensure timely completion of coding tasks.

London, England, United Kingdom

• Performs the medical coding and review of clinical data for the clinical research programmes of IPSEN Group in an accurate, consistent and timely manner in accordance with the company standard medical coding guidelines• Ensures the coding manuals were used to review and resolve MedDRA and WHO-DD failures by coding terms, or generating/issuing queries as appropriate• Upgrade of dictionary versions

London, England, United Kingdom

Harlow, Hertfordshire

• Data management for Phase 1 Neuroscience studies, from set up to lock• Working with the Study Team to define requirements for Inform databases for various studies• Programming and/or working with external programmers to set up Inform database• The testing and validation of Inform databases• Worked with remaining Paper Studies

Harlow, Hertfordshire

• Providing technical support to output data for Medical Physicians to be able to examine trends in medical and drug data• Migration and review of Pharmacovigilance data to new systems with the Safety scientists and physicians

Harlow, Hertfordshire

• Development and implementation of departmental organizational structure & performance measures• Heading a Therapeutic area team with coordination of workload and coding/reviewing management• Heading a Functional Team, coordinating the improvement of MedDRA-related processes and systems• Contributed to GSK systems upgrades and heading the GSK MedDRA migration sub-team• GSK Dictionary system implementation