Life Sciences Jobs CT Submission Specialist at BMS Hyderabad
CT Submission Specialist opportunity at BMS for life sciences professionals
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CT Submission Specialist – Life Sciences Jobs at BMS | Apply Now

Looking to advance your career through impactful life sciences jobs? BMS is hiring for CT Submission Specialist Jobs in Hyderabad, offering professionals the opportunity to support FDA submissions and global clinical trial documentation. This role is ideal for candidates seeking structured growth in regulatory operations, clinical trial transparency, and document management within a globally recognized biopharmaceutical company.

  • Job Title: CT Submission Specialist
  • Location: Hyderabad
  • Job ID: R1596335

About the Company:

Bristol Myers Squibb (BMS) is a leading global biopharmaceutical company driven by the mission to transform patients’ lives through science. Known for innovation, inclusion, and integrity, BMS provides professionals with a collaborative environment where life sciences jobs directly contribute to life-changing therapies across oncology, immunology, and cell therapy.

Job Overview:

The CT Submission Specialist role at BMS supports the preparation, coordination, and quality review of clinical trial submission documents for regulatory authorities. The position works closely with Global Development Operations teams to ensure submission-ready compliance, timely delivery, and adherence to ICH, GCP, and FDA regulatory standards.

Key Responsibilities:

  • Support preparation and QC of clinical trial submission documents
  • Coordinate FDA submission deliverables within GDO teams
  • Ensure submission documents meet SRC requirements
  • Partner with Clinical Trial Support Specialists for document timelines
  • Review CSR appendices, financial disclosure tables, and related documents
  • Identify risks and escalate submission issues appropriately
  • Support trial transparency and regulatory compliance activities

Educational Requirements:

  • Bachelor’s degree in Life Sciences, or equivalent

Skills Required:

  • Strong understanding of clinical trial documentation and submissions
  • Knowledge of ICH, GCP, and regulatory guidelines
  • Experience with CTMS and document management systems
  • Familiarity with Veeva Vault Clinical and TMF systems
  • Strong communication, organizational, and project management skills

CT Submission Specialist Jobs at BMS offer professionals a unique opportunity to build meaningful careers in life sciences jobs. With exposure to global regulatory submissions and clinical development operations, this role provides long-term growth, professional stability, and purpose-driven work.

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