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Job Overview

  • Date Posted
  • Location (State / UT)
  • Expiration date
  • Experience
    8 Years
  • Gender
  • Desired Qualification
    Bachelor Degree, Master’s Degree, Doctorate Degree
  • Salary in (₹)

Job Description

Department – Global Safety GBS – SO Clinical Case Management

Category:  Clinical Development and Medical
Location: Bangalore, Karnataka, IN

The position:

As a Team Leader – you will be part of a diverse and dynamic team currently consisting of 62 dedicated employees, whereas the key responsibility of this position relies on Managing the Department including coaching/mentoring/training/support of direct reports and development plan process, driving continuous improvements, contribute to setting the direction for Global Safety-Global Business Support, ensuring that the business targets for the department are met. Resource planning and prioritization of department tasks to ensure optimal and flexible use of resources (including timely identification and resolution of resource gaps), and monitoring and reporting of department performance.

Team Leader is the primary driver in the process of optimisation of the operational case handling of serious adverse events, non-serious adverse events, and pregnancies on products. Contribute to the build-up of a strong team, which can work professionally in the operational handling of adverse events in close collaboration with affiliates and other partners. The tasks demand self-dependence and competence in making decisions, as well as flexibility, a good comprehensive view, and many-functioned, often international, cooperation. Maintain a network of safety contacts within HQ and affiliates.

  • Evaluate performance, job descriptions, and individual development plans for employees. Supervise the daily activity of the team, including vacation, planning, and other activities.
  • Ensure continuous development of employees, training/coaching in pharmacovigilance and in departmental functions as well as provision of knowledge about NN business. Monitor and ensure that KPIs for evaluation and reporting of adverse events is maintained.
  • To participate in the development and maintenance of departmental and functional procedures which have to ensure the observance of internal and external requirements for the management of safety information.
  • Close cooperation with other groups in Global Safety. Liaise with the Safety Reporting and IT in all aspects of E2B reporting; database and application management; data retrieval; custom reporting. Provide input to safety data exchange agreements and pharmacovigilance system description documents regarding the post-marketing surveillance process.
  • Establish and maintain effective project communications by representing the department at interdepartmental project team meetings to understand and adhere to the specific safety reporting requirement. Prepare for and/or participate in audits and inspections.
  • Bachelor’s degree is required. An educational background as a B. Pharm / B.D.S / M. Pharm / Life sciences is preferred.
  • A minimum of eight 8 or more years of Pharma industry experience or Pharmacovigilance experience
  • Solid knowledge of pharmacovigilance principles and international regulatory requirements regarding drug safety.
  • Ability to analyze quickly, yet with strict attention to minute detail, plan time and approaches to problems, and exercise creativity and judgment in resolving issues.
  • Being open-minded, curious, and willing to experiment to learn is part of our culture.
  • Dynamic, eager to learn, and have a strong quality mindset, able to create a dynamic and trusting environment.
  • Value different perspectives and display inclusive and cooperative behavior, proactive, and can quickly adapt to new and changing environments.
  • Should have a global mindset and enjoy building relations across organizational levels and geography learn and adapt quickly.
  • Excellent oral and written communication skills.

Apply on or Before 10th Feb 2023