Data Entry Associate
6 months ago
Looking to jump-start your career?
We understand how important the first few years of your career are, which create the foundation of your entire professional journey. At Indegene, we promise you a differentiated career experience. You will not only work at the exciting intersection of healthcare and technology but also will be mentored by some of the most brilliant minds in the industry. We are offering a global fast track career where you can grow along with Indegene’s high-speed growth.
We are purpose-driven.
** **We enable healthcare organizations be future ready and our customer obsession is our driving force
**.** We ensure that our customers achieve what they truly want. We are bold in our actions, nimble in our decision-making, and industrious in the way we work.
**Data Entry Associate**
**You will be responsible for**:
"Confirm validity of case by identifying minimum criteria for case creation.
- Perform duplicate search to create either an initial case or a follow-up case.
- Understanding the principles and concepts associated with patient safety case-handling
process including regulatory requirements for reporting individual case safety reports.
- Identify serious adverse events and special scenario cases which includes lack of efficacy,
exposure, and pregnancy case, at risk cases, and product quality complaint only cases.
- Attach the relevant source documents or any safety information/queries/follow-up
information that is relevant to the case.
- Facilitate follow-up based on queries from Data entry/QC/MR or based on
inconsistent/missing information in the source file.
Responsible for coding which includes adverse event, medical history, Lab data, Indications
etc using standardized terminology from a medical coding dictionary, such as MedDRA.
- Code products (Suspect/co-suspect, Concomitant) as per Client conventions and Regulatory
requirements.
- Draft narratives."
**Your impact**:
**About you**:(Desired profile)
**Must have**:Understand the principles and concepts associated with case-handling process and overall Drug Research Process. - Cognitive abilities including verbal reasoning, attention to detail, and critical and analytical thinking. - Good knowledge on therapy area/medical terminology. - Good comprehension skills. - Good communication (verbal and written), with fluency in English and interpersonal skills.
**EQUAL OPPORTUNITY**
We are an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, national origin, gender identity, sexual orientation, disability status, protected veteran status, or any other characteristics.
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