Senior Programmer for Pharmaceutical Industry

1 week ago

Bengaluru, Karnataka, India beBeeProgrammer Full time ₹ 1,04,000 - ₹ 1,30,878

A senior programmer is required to work as part of a statistical and programming team.

The role entails various responsibilities, including programming support, attending internal and client study team meetings, and mentoring less experienced team members.

Daily interactions involve communicating directly with other study team members and client key contacts, sharing updates on ongoing work, and collaborating with the internal team to deliver high-quality work on time.

Key responsibilities include:

  • Programming and QC datasets following specifications and good practice
  • Developing dataset specifications that conform to CDISC data standards
  • Attending and contributing to internal and client study team meetings
  • Mentoring less experienced team members

Additionally, the role involves daily interactions such as:

  • Communicating directly with other study team members and client key contacts
  • Sharing updates on ongoing work internally and at client meetings
  • Collaborating with the internal Veramed team to deliver high quality work on time
  • Contribute programming expertise and wider industry knowledge as required
  • Provide support and mentoring for more inexperienced members on the team

This role provides opportunities for growth and development into lead programmer or technical roles, gaining experience across different therapeutic areas and phases, presenting at conferences, peer mentoring and/or line management, developing innovative solutions, and contributing to initiatives that consider employees, the environment, and local communities.

A warm, friendly working environment is provided, along with a supportive, open-door management policy that aids in development and career progression. Exposure to a wide range of clients and projects allows for diversification of workload and close collaboration with leading pharma companies. The ability to own the role and develop skills and experience is also available.

Beneficial experience includes understanding of the clinical drug development process, awareness of industry and project standards, proficiency in using SAS or other statistical software, a good understanding of CDISC data standards, self-management skills, and ability to work independently and as part of a team.

This role is ideal for those passionate about contributing to high-quality deliverables, working closely with team members, and wanting to add value to a company.

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