At Sun Pharma, we commit to helping you “Create your own sunshine”— by fostering an environment where you grow at every step, take charge of your journey and thrive in a supportive community.
As you enter the Sun Pharma world, you’ll find yourself becoming ‘Better every day’ through continuous progress. Exhibit self-drive as you ‘Take charge’ and lead with confidence. Additionally, demonstrate a collaborative spirit, knowing that we ‘Thrive together’ and support each other’s journeys.”
Key Roles & Responsibilities
- Perform clinical data coding activities across assigned projects/program.
- May perform impact analysis for Medical Coding using MedDRA, WHO Drug and/or other relevant dictionary up versioning or as applicable.
- Validates/tests the coding set up and programming of coding reports; may also test databases, edit specifications or any coding related programming activities.
- Conduct data review (including but not limited to medical data review)
- Write and resolve data inconsistencies/discrepancies.
- May perform Serious Adverse Event (SAE) reconciliation activities.
- Works in strict adherence to SOPs and other applicable standards in compliance with Sun Procedural Documents, ICH-GCP and local regulations.
- Develop and maintain good communications and working relationships with the global clinical data management team.
- Additionally, can perform Clinical Data Management Reviewer role, if trained and as assigned under the guidance of Clinical Data Management Project Lead.
CompetenciesRequired:
- Minimum 3 years of clinical data coding experience including working knowledge using clinical data coding tools and applications.
- Experience of leading clinical data coding effort across global clinical studies preferred.
