Drug Safety Associate

0-3 years

Not Disclosed

Bangalore

10 March 4, 2024

Job Description

Job Type: Full Time Education: Any Graduate Skills: Communication Skills, Interpersonal Skill, Technical Skill

About the job

We are a technology-led healthcare solutions provider. We are driven by our purpose to enable healthcare organizations to be future ready. We offer accelerated, global growth opportunities for talent that’s bold, industrious and nimble. With Indegene, you gain a unique career experience that celebrates entrepreneurship, and is guided by passion, innovation, collaboration and empathy. To explore exciting opportunities at the convergence of healthcare and technology, check out www.careers.indegene.com

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.

If this excites you, then apply below.

Drug Safety 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:

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
Looking for Immediate Joiners only

EQUAL OPPORTUNITY

Indegene is proud to be an Equal Employment Employer and is committed to the culture of Inclusion and Diversity. We do not discriminate on the basis of race, religion, sex, colour, age, national origin, pregnancy, sexual orientation, physical ability, or any other characteristics. All employment decisions, from hiring to separation, will be based on business requirements, candidate’s merit and qualification.

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.

Latest Jobs

Pharma Jobs in India

Pharma Jobs in United States

Pharma Jobs in Germany

Pharma Jobs in Australia & England & Europe & Ireland & Remote & Saudi Arabia

Drug Safety Associate

Job Description

About the job

Latest Jobs

Senior Clinical Data Manager

Clinical Document Specialist, Clinical Documentation Management

Clinical Document Specialist, Clinical Documentation Management

Clinical Research Associate Ii

Clinical Research Associate

Senior Clinical Research Associate Ii

Medical Information And Adverse Event Intake Specialist

Scientific Specialist

Pharmacovigilance (Qppv)

Senior Pharmacovigilance (Pv) Compliance Manager

Pharma Jobs in India

Pharma Jobs in United States

Pharma Jobs in Germany

Pharma Jobs in Australia & England & Europe & Ireland & Remote & Saudi Arabia