Associate Data Manager

0-1 years

Not Disclosed

Bangalore

10 March 22, 2024

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm Skills: Causality Assessment, Communication Skills, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Narrative Writing, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Data Manager

Category: Data & AI

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.

Working At Novo Nordisk

At Novo Nordisk, we are driving change to defeat diabetes and other serious chronic conditions. Our treatments today are benefiting millions of people living with diabetes, obesity, and rare blood and endocrine diseases. From our labs to our factory floors, we are discovering and developing innovative biological medicines and making them accessible to patients throughout the world. Since the company was founded in Denmark more than 100 years ago, we have been translating the unmet medical needs of people living with serious chronic diseases into innovative medicines and delivery. Our focus is on these diseases, which affect hundreds of millions of people and are among the most urgent global health challenges. By combining our innovation and commercial excellence, we draw upon insights from patients and partners to transform bold ideas into life-saving and preventive medicines. Our ambition is to take the lead in each of these areas, driving change with an unfailing belief that it can be done.

Contact

To submit your application, please upload your CV online (click on Apply and follow the instructions).

Apply Now!

Deadline

31st March 2024.

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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