Novo Nordisk A/S is a Danish multinational pharmaceutical company and is currently hiring for the position mentioned below. Read the complete notification before applying
Role;- Associate Data Manager
Location: Bangalore, Karnataka, IN
Department –Trial Data Management
Are you passionate about quality and simplification? Do you want to build quality within processes in the most efficient way? Do you have an innovative mindset to drive change in a future-ready environment and support your colleagues and stakeholders by challenging the status-quo in a friendly and open-minded way? If so, there is a job opportunity waiting for you as our new Associate Data Manager. At Novo Nordisk, we will challenge you to do the best work of your life. Apply Now.
About the Department
The Trial data management department was established in Bangalore, India in the month of September 2007 and has significantly grown. It is a young, enthusiastic, and dynamic team with varied skillsets and professionals from diverse backgrounds such as pharmacy, life-sciences, physiotherapy, computer/information sciences and business administration. The key objective of the department is to ensure high quality data delivery to the stakeholders. The involvement of various groups in data management is significant in key stages of trial setup, conduct and closeout.
The Position:
The Associate Data Manager will coordinate and ensure timely completion of discrepancy Management activities for assigned projects following appropriate regulatory guidelines, company, and department SOPs. The Associate Data Manager should secure that all trial work is adhered to current DM standards. Responsible to review basic data and discrepancy review should be done with a DM perspective with reference to NN procedures and instructions and by common DM knowledge in an acceptable standard.
- The Associate Data Manager should be able to identify risks and incorporate preventive/mitigating actions in the plan. Responsible for supporting end users and must act independently, following the strategic objectives of the standards governance bodies and the company in general is recognized as responsible for supporting end users and must act independently, following the strategic objectives of the standards governance bodies and the company in general.
- The Associate Data Manager should have attention on irregularities, deviations and should therefore arrive for the probable solutions for the foreseen risks and thus to decide on the relevant proposals for actions.
- Ensuring the integrity of clinical trial databases. Perform basic data and discrepancy review Write data clarifications and resolve/update as per trial requirements.
- Develop and maintain good communications and working relationships with Trial Data Management team. Perform UAT of the database as directed by the Clinical Project Lead (CPL).
- Responsible to Review basic data and discrepancy review should be done with a DM perspective with reference to NN procedures and instructions and by common DM knowledge in an acceptable standard.
Qualification:
- MSc/BSc in Natural/Life Science or comparable degree in medicine, nursing, pharmacy, veterinary science or clinical information management or equivalent qualifications
- Preferably a degree in computer science or equivalent professional experience.
- Preferably 0-2 years of data management experience and the majority of this within Pharma Industry or Development.
- Preferably knowledge of clinical development.
- Ability to build and maintain solid internal networks.
- Good communication, presentation, and negotiation skills
- Ability to plan well and handle complex tasks simultaneously and independently.
- Good team player with communication and stakeholder management skills.
- Analytical and result oriented.
- Proactive and resilient to changes.
Contact
To submit your application, please upload your CV online (click on Apply and follow the instructions).
Apply Now!
Deadline
31st March 2024.
