Medical Reviewer Professional

Novo Nordisk

2 - 5 years

4 - 8 Lacs

bengaluru

Posted:-1 days ago| Platform:

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Skills Required

medical mbbs data cleaning gcp stakeholder management compliance data systems clinical trials pharmacovigilance

Work Mode

Work from Office

Job Type

Full Time

Job Description

The Key Responsibilities

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

We are looking for a highly skilled and motivated individual who meets the following criteria:

A graduate degree in MBBS+MD with 2 to 5 years of experience
Good knowledge of ICH GCP guidelines.
Demonstrated computer skills (MS Office, MS Project, PowerPoint).
Excellent understanding of medical terminology and clinical trial activities, Experience with risk-based monitoring methodologies. - Familiarity with clinical trial data systems and tools.
Excellent written and spoken English, Strong analytical and result-oriented skills, Ability to plan and handle complex tasks independently, good communication and stakeholder management skills

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