Novo Nordisk•18 days ago
Associate Functional Programmer
Recruiter Fit Breakdown & Candid Summary
1
This role is ideal for junior professionals with 1-3 years of experience in the pharmaceutical or clinical data space looking to apply programming skills to clinical trials.
2
Candidates will work on generating standard and custom monitoring reports using various data and BI tools while ensuring data integrity.
3
Those without a background in life sciences, clinical data, or basic programming in languages like SAS, SQL, Python, or R should not apply.
Role Responsibilities
- 1Generate and maintain standard and customised monitoring reports including Trial, Central, Medical Monitoring, and Risk Indicator reports.
- 2Develop new programs or customise existing ones using tools such as Central Monitoring Platform (CMP), Qlik Sense, SQL, SAS, JMP, Power BI, Databricks, Pyt
- 3Translate stakeholder requirements into detailed specifications for report development.
- 4Produce ad-hoc reports for stakeholders covering adverse events, data cleaning cycles, protocol deviations, and subject lists.
- 5Create validation documentation, conduct peer reviews, and design report templates using data models or mock data.
- 6Participate in monitoring report meetings, record minutes, and follow up on action items.
Skills Matrix
Must-Have Skills
SAS
SQL
Python
General Competency
Qlik Sense
Power BI
Databricks
Nice-to-Have Skills
No optional skills specified for this role.
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