Consultant Technology

Reposted 4 Days Ago
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Noida, Gautam Buddha Nagar, Uttar Pradesh, IND
Hybrid
Junior
Biotech • Pharmaceutical
The Role
Develop, unit-test, and troubleshoot data migrations for safety systems. Translate mapping specs into migration code and queries, collaborate with testing and validation, and take ownership of assigned modules.
Summary Generated by Built In
Company Description

This position is working for Prudentia, a PrimeVigilance company.

We are PrimeVigilance (part of Ergomed Group), a specialised mid-size pharmacovigilance service provider established in 2008. We are proud to have achieved global organic growth year after year, with staff based across Europe, North America and Asia all covering services within: Medical Information, Pharmacovigilance, Regulatory Affairs and Quality Assurance. 

PrimeVigilance provides first class support to our small to large pharmaceutical and biotechnology partners maintaining long lasting relationships and has become one of the global leaders in its field. We cover all therapy areas including medical device. 

We love investing in our staff by providing an excellent training and development platform. We value employee experience, well-being and mental health and we acknowledge that a healthy work life balance is a critical factor for employee satisfaction and in turn nurtures an environment from which a high-quality client service can be achieved. 

Come and join us in this exciting journey to make a positive impact in patient’s lives.  

Job Description

Responsible for development and unit testing of data migrations for safety systems. Should have good SQL knowledge to be able to develop migration code based on requirements. The work would involve understanding requirements, developing the code based on the requirements, working with testing team in identifying and resolving issues, and working with full ownership and responsibility of the assigned modules.

  • Assist with defining data migration requirements
  • Understand data migration requirements and mapping specifications
  • Develop data migration code and testing queries
  • Troubleshoot and resolve data migration issues
  • Collaborate with team members across development and validation

Qualifications

  • Computer science, Information Technology graduate
  • Minimum 2 years of experience in data migrations
  • Excellent analytical and problem-solving skills
  • Strong communication skills
  • Back-end and application knowledge of Argus
  • Strong SQL and PLSQL skills

Additional Information

We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders and ages can contribute and grow.  

To succeed we must work together with a human first approach. Why? because our people are our greatest strength leading to our continued success on improving the lives of those around us. 

We offer: 

  • Training and career development opportunities internally  

  • Strong emphasis on personal and professional growth 

  • Friendly, supportive working environment 

  • Opportunity to work with colleagues based all over the world, with English as the company language 

Our core values are key to how we operate, and if you feel they resonate with you then PrimeVigilance could be a great company to join!  

  • Quality 

  • Integrity & Trust  

  • Drive & Passion  

  • Agility & Responsiveness  

  • Belonging 

  • Collaborative Partnerships  

We look forward to welcoming your application. 

Top Skills

Argus
Plsql
SQL
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The Company
HQ: Raleigh, NC
535 Employees
Year Founded: 1997

What We Do

Founded in 1997, Ergomed is a global provider of high-quality services to the biopharmaceutical industry, spanning all phases of clinical trials, post-approval pharmacovigilance, and medical information. Ergomed’s fast-growing services business includes an industry-leading suite of specialist pharmacovigilance (PV) solutions, integrated under the PrimeVigilance brand, and Ergomed Clinical Research, a complete, global Phase I-IV clinical development and trial management services with a strong heritage in the development of drugs in rare diseases and oncology. • 1,400+ highly qualified professionals • Global full-service CRO • 25+ years of experience • Therapeutic specialization in oncology • Strong expertise in rare disease trials • Robust clinical safety system • Choice of leading drug safety databases Our key services include: • Clinical Research Services • Pharmacovigilance • Medical Information • Regulatory • Medical Writing • Site Management • Study Physician Support • Biostatistics • Patient Study Support

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