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Exciting Job Opportunities at Fortrea: Join Us as a Programmer Analyst, Senior Safety Writer, or Senior Principal Statistical Programmer!

Job highlights

Work/Life Balance

Time management

challenging projects

Insurance

Are you looking for a rewarding career in the pharmaceutical and clinical research industry? Fortrea is hiring for three key roles that offer tremendous growth opportunities and the chance to make a significant impact on global health.

About Fortrea

Fortrea is a leading global provider of drug development and data solution services, delivering quality and reliable results with the highest standards of compliance. Our mission is to enhance patient outcomes through strategic and innovative approaches to clinical research. With a robust workforce dedicated to excellence, we pave the way for new therapies and advance healthcare solutions worldwide.

Open Positions

We have three exciting job openings:

1. Programmer Analyst

Location: Remote (Bangalore)
Job Requisition ID: 25836
Employment Type: Full-time
Apply By: March 21, 2025

Job Description:
As a Programmer Analyst, you will engage in independent programming activities, primarily using Medidata Rave or SAS, across multiple projects. You’ll develop solutions to technical issues pertaining to EDC tools, maintain study databases, and create programming specifications for dataset creation.

Responsibilities:

  • Perform SAS programming for dataset creation and quality control.
  • Collaborate in developing visual analytics dashboards using tools like Spotfire/Tableau.
  • Mentor team members on EDC tools and SAS programming.
  • Ensure compliance with regulations and Fortrea SOPs.

2. Senior Safety Writer

Location: Mumbai
Job Requisition ID: 25953
Employment Type: Full-time
Apply By: March 21, 2025

Job Description:
In this role, you will lead the preparation and review of aggregate safety reports, ensuring timely delivery of quality documents. Utilizing your safety domain knowledge, you will manage project scope and responsibilities while coaching junior team members.

Responsibilities:

  • Write and review safety reports for global regulatory submissions.
  • Draft responses to health authority questions and collaborate with stakeholders.
  • Conduct signal detection activities and author signal reports.
  • Mentor and train medical writers and junior associates.

3. Senior Principal Statistical Programmer

Location: Bangalore
Job Requisition ID: 251355
Employment Type: Full-time
Apply By: March 18, 2025

Job Description:
As a Senior Principal Statistical Programmer, you will lead statistical programming activities, from study set-up to completion. You will guide programmers, develop complex SDTM and ADaM datasets, and mentor team members effectively.

Responsibilities:

  • Oversee all programming activities for clinical studies.
  • Develop and maintain SAS programs and define XML/PDFs.
  • Respond to QA and client audits, improving efficiency within the team.
  • Mentor junior programmers on best practices and processes.

Qualifications Required

For all positions, a degree in life sciences or relevant technical fields is essential. Candidates must also have a strong command of English and excellent communication skills. Experience in the pharmaceutical industry is highly desired, with specific role requirements varying by position, such as SAS programming proficiency for the Programmer Analyst and statistical programming expertise for the Senior Principal Statistical Programmer.

Application Link For Programmer Analyst

Application Link For Senior Safety Writer

Application Link For Senior Principal Statistical Programmer

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