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Worldwide Clinical Trials — фармацевтикалық және биотехнологиялық компанияларға дәрі-дәрмек әзірлеудің бүкіл үдерісі бойы қолдау көрсететін жаһандық келісімшарттық зерттеу ұйымы. 30 жылдан астам тәжірибесі бар компания онкология, кардиология және сирек кездесетін ауруларды қоса алғанда, әртүрлі терапиялық бағыттарда клиникалық мониторинг, деректерді басқару, пациенттерді тарту және реттеушілік кеңес беру қызметтерін ұсынады. Оның тәсілі клиникалық зерттеулер саласындағы кең ауқымды сараптаманы күрделі зерттеулерге арналған жекелендірілген қолдау және бейімделген шешімдермен ұштастырады.
Senior Clinical Coding Specialist
Support clinical trial coding at Worldwide Clinical Trials by maintaining medical dictionaries, ensuring coding quality, preparing sponsor reports, and mentoring junior colleagues.
Сипаттама
- Support study start-up coding for existing and new EDC databases.
- Contribute to Data Management Plans and conduct User Acceptance Testing, including reviews of database specifications and CRFs.
- Manually code medical and medication terms.
- Prepare and check coding consistency reports for accuracy.
- Submit coding reports for Medical Monitor, peer, and sponsor reviews at project-defined intervals.
- Coordinate medical dictionary implementation and version updates.
- Work with sponsors to address general and project-specific coding matters.
- Deliver consistent, high-quality coding within study timelines.
- Coordinate dictionary licence validation and Worldwide licence renewals.
- Improve coding processes and technology, track results, and recommend next steps.
- Lead and mentor junior staff carrying out coding work.
- Attend sponsor and team meetings as needed.
- Track study coding budgets and potential CIS/OOS issues.
- Update management on coding deliverables, metrics, and issues.
- Ensure clinical coding operations comply with WCT SOPs.
- Provide cover for the Manager of Clinical Coding and Data Management.
- Carry out other assigned duties.
Талаптар
- A degree, preferably in life sciences, a nursing qualification, or relevant industry experience.
- Training or experience coding with standard industry dictionaries such as MedDRA and WHO-DD.
- At least three years of clinical data coding or related experience in the pharmaceutical, biotechnology, or medical device industries.
- Computer and numeracy skills, with willingness to adapt to different systems.
- Careful attention to detail and readiness to question the validity of entered data.
- Strong time-management and people-management skills.
- Ability to prioritize and handle multiple coding tasks and workloads.
- Strong interpersonal and communication skills.
- Ability to work effectively in a global environment.
Артықшылықтар
- Equal employment opportunity regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or any other class protected by applicable law.
- A diverse and inclusive workplace.
- Supportive, collaborative teams.
- Accessible leadership.
- A positive employee experience.
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