Associate Medical Reviewer

2 weeks ago

Bengaluru, India Novo Nordisk Full time

Associate Medical Reviewer

**Category**:Clinical Development**Location**:Bangalore, Karnataka, IN**Department - Centralised Monitoring Unit (CMU)
- Bangalore**About the Department**:

- The Centralised Monitoring Unit (CMU)
- Bangalore, is a department within the Clinical Drug Development area. It is a perfect blend of skilled medical professionals (Medical reviewers) and technical programmers (Functional programmers, statistical monitors). Medical reviewers actively involved in Risk based medical monitoring in collaboration with the medical specialists from Denmark, with focus on ensuring overall patient safety and wellbeing of all clinical trial participants, by ensuring compliance to protocol and identifying potential clinically significant outliers that requires medical attention and medical data cleaning. The Functional Programmers develop operational visualisations in data visualization tools to support the trial teams on proactive centralised monitoring and Statistical Monitors perform detection of unusual data patterns, systematic errors and potential lack of compliance or fraud across trials.**The Position**:
- Responsible for contribution to or participation in trial planning activities related to medical review.
- Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites.
- Responsible for presenting findings of Medical Review to relevant Medical Specialist to enable decision making. Responsible for documenting medical review in the sponsor TMF.
- Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialist during trial conduct.
- Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform Medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review.

**Qualifications**:

- Minimum as Postgraduate in Medicine or other relevant (MBBS & MD in pharmacology preferred, MBBS & MD in other clinical/paraclinical areas with relevant experience in clinical patient management/ clinical research).
- 1 years of experience as Medical Reviewer is preferred.
- Good knowledge of ICH(International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use), GCP (Good clinical Practice).
- Demonstrated computer skills (MS Office, MS Project, PowerPoint).
- Excellent understanding of medical terminology and clinical trial activities.
- Excellent written and spoken English.

**Working at Novo Nordisk**
- At Novo Nordisk, we create value by putting patients first. Every ten seconds two people are diagnosed with diabetes, and more than 371 million people worldwide need us. Working here is not just a way to make a living, but a way to make a difference.**Contact**-
**Deadline**
- 15th November 2023- We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.- At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

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