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Bristol-Myers Squibb logo

Senior Manager - Submission Management

Bristol-Myers Squibb

Senior Manager - Submission Management

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 21, 2025

Number of Vacancies: 1

Job Description

Regulatory Strategy & Submission Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines. Assess core submission deliverables to ensure compliance, prepare and deliver eCTD submission dossiers for global markets. Drive the execution of the Global Submission Plan for assigned products, collaborating with global teams and proactively monitoring progress to ensure timely health authority submissions. Manage the submission production activities for assigned products including the lifecycle management of applications. Manage the submission production activities for queries, commitments, and other lifecycle management submissions with health authorities. Continuous Improvement Initiatives Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams. Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information. Ensure consistency of IND and marketing applications across projects, studies, and countries, aligning with regulatory standards and best practices. Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement. Apply now and help us shape the next generation of Submissions Manager - Clinical Trials! Lead a team of direct reports managing resource and allocation and assigned projects, provide training and mentoring to new staff, and support team with development and innovation. 7+ years relevant submissions experience and people management experience. Proficient knowledge of global regulatory practices, submission guidelines and requirements. Collaborates with key stakeholders and resolves cross-functional issues independently and generates solutions by weighing risks and dependencies. Support of other RISM members sharing expertise, providing guidance and serving as a SME. Communicates effectively in English and simplifies complex topics for presentations and workshops. Applies project management methodologies and strategic thinking to define objectives, track progress, and deliver results on increasingly more complex projects. Proficient with desktop software and able to instruct others. Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned.

About the Role/Company

  • The company focuses on shaping the next generation of Submissions Manager - Clinical Trials
  • The company values innovation and continuous improvement in regulatory processes

Key Responsibilities

  • Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements
  • Ensure alignment with regulatory standards and project timelines
  • Assess core submission deliverables to ensure compliance
  • Prepare and deliver eCTD submission dossiers for global markets
  • Drive the execution of the Global Submission Plan for assigned products
  • Collaborate with global teams and monitor progress to ensure timely health authority submissions
  • Manage submission production activities for assigned products including lifecycle management of applications
  • Manage submission production activities for queries, commitments, and other lifecycle management submissions with health authorities
  • Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams
  • Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information
  • Ensure consistency of IND and marketing applications across projects, studies, and countries
  • Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement
  • Lead a team of direct reports, managing resource allocation and assigned projects
  • Provide training and mentoring to new staff
  • Support team with development and innovation

Required Qualifications

  • + years of relevant submissions experience
  • People management experience
  • Proficient knowledge of global regulatory practices, submission guidelines, and requirements

Skills Required

  • Collaboration with key stakeholders
  • Resolution of cross-functional issues independently
  • Generation of solutions by weighing risks and dependencies
  • Effective communication in English
  • Simplification of complex topics for presentations and workshops
  • Application of project management methodologies and strategic thinking
  • Proficiency with desktop software and ability to instruct others

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Collaboration with key stakeholdersintermediate
  • Resolution of cross-functional issues independentlyintermediate
  • Generation of solutions by weighing risks and dependenciesintermediate
  • Effective communication in Englishintermediate
  • Simplification of complex topics for presentations and workshopsintermediate
  • Application of project management methodologies and strategic thinkingintermediate
  • Proficiency with desktop software and ability to instruct othersintermediate

Required Qualifications

  • + years of relevant submissions experience (experience)
  • People management experience (experience)
  • Proficient knowledge of global regulatory practices, submission guidelines, and requirements (experience)

Responsibilities

  • Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements
  • Ensure alignment with regulatory standards and project timelines
  • Assess core submission deliverables to ensure compliance
  • Prepare and deliver eCTD submission dossiers for global markets
  • Drive the execution of the Global Submission Plan for assigned products
  • Collaborate with global teams and monitor progress to ensure timely health authority submissions
  • Manage submission production activities for assigned products including lifecycle management of applications
  • Manage submission production activities for queries, commitments, and other lifecycle management submissions with health authorities
  • Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams
  • Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information
  • Ensure consistency of IND and marketing applications across projects, studies, and countries
  • Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement
  • Lead a team of direct reports, managing resource allocation and assigned projects
  • Provide training and mentoring to new staff
  • Support team with development and innovation

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Bristol-Myers Squibb logo

Senior Manager - Submission Management

Bristol-Myers Squibb

Senior Manager - Submission Management

Bristol-Myers Squibb logo

Bristol-Myers Squibb

full-time

Posted: November 21, 2025

Number of Vacancies: 1

Job Description

Regulatory Strategy & Submission Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements, ensuring alignment with regulatory standards and project timelines. Assess core submission deliverables to ensure compliance, prepare and deliver eCTD submission dossiers for global markets. Drive the execution of the Global Submission Plan for assigned products, collaborating with global teams and proactively monitoring progress to ensure timely health authority submissions. Manage the submission production activities for assigned products including the lifecycle management of applications. Manage the submission production activities for queries, commitments, and other lifecycle management submissions with health authorities. Continuous Improvement Initiatives Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams. Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information. Ensure consistency of IND and marketing applications across projects, studies, and countries, aligning with regulatory standards and best practices. Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement. Apply now and help us shape the next generation of Submissions Manager - Clinical Trials! Lead a team of direct reports managing resource and allocation and assigned projects, provide training and mentoring to new staff, and support team with development and innovation. 7+ years relevant submissions experience and people management experience. Proficient knowledge of global regulatory practices, submission guidelines and requirements. Collaborates with key stakeholders and resolves cross-functional issues independently and generates solutions by weighing risks and dependencies. Support of other RISM members sharing expertise, providing guidance and serving as a SME. Communicates effectively in English and simplifies complex topics for presentations and workshops. Applies project management methodologies and strategic thinking to define objectives, track progress, and deliver results on increasingly more complex projects. Proficient with desktop software and able to instruct others. Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned.

About the Role/Company

  • The company focuses on shaping the next generation of Submissions Manager - Clinical Trials
  • The company values innovation and continuous improvement in regulatory processes

Key Responsibilities

  • Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements
  • Ensure alignment with regulatory standards and project timelines
  • Assess core submission deliverables to ensure compliance
  • Prepare and deliver eCTD submission dossiers for global markets
  • Drive the execution of the Global Submission Plan for assigned products
  • Collaborate with global teams and monitor progress to ensure timely health authority submissions
  • Manage submission production activities for assigned products including lifecycle management of applications
  • Manage submission production activities for queries, commitments, and other lifecycle management submissions with health authorities
  • Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams
  • Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information
  • Ensure consistency of IND and marketing applications across projects, studies, and countries
  • Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement
  • Lead a team of direct reports, managing resource allocation and assigned projects
  • Provide training and mentoring to new staff
  • Support team with development and innovation

Required Qualifications

  • + years of relevant submissions experience
  • People management experience
  • Proficient knowledge of global regulatory practices, submission guidelines, and requirements

Skills Required

  • Collaboration with key stakeholders
  • Resolution of cross-functional issues independently
  • Generation of solutions by weighing risks and dependencies
  • Effective communication in English
  • Simplification of complex topics for presentations and workshops
  • Application of project management methodologies and strategic thinking
  • Proficiency with desktop software and ability to instruct others

Locations

  • Warsaw, United States

Salary

Salary not disclosed

Estimated Salary Rangemedium confidence

150,000 - 220,000 USD / yearly

Source: ai estimated

* This is an estimated range based on market data and may vary based on experience and qualifications.

Skills Required

  • Collaboration with key stakeholdersintermediate
  • Resolution of cross-functional issues independentlyintermediate
  • Generation of solutions by weighing risks and dependenciesintermediate
  • Effective communication in Englishintermediate
  • Simplification of complex topics for presentations and workshopsintermediate
  • Application of project management methodologies and strategic thinkingintermediate
  • Proficiency with desktop software and ability to instruct othersintermediate

Required Qualifications

  • + years of relevant submissions experience (experience)
  • People management experience (experience)
  • Proficient knowledge of global regulatory practices, submission guidelines, and requirements (experience)

Responsibilities

  • Collaborate with key stakeholders to define IND and marketing submission strategies and document requirements
  • Ensure alignment with regulatory standards and project timelines
  • Assess core submission deliverables to ensure compliance
  • Prepare and deliver eCTD submission dossiers for global markets
  • Drive the execution of the Global Submission Plan for assigned products
  • Collaborate with global teams and monitor progress to ensure timely health authority submissions
  • Manage submission production activities for assigned products including lifecycle management of applications
  • Manage submission production activities for queries, commitments, and other lifecycle management submissions with health authorities
  • Drive initiatives that promote innovation and simplify processes to enhance efficiencies for BMS teams
  • Contribute to the ongoing maintenance of regulatory requirements to ensure accurate and current regulatory information
  • Ensure consistency of IND and marketing applications across projects, studies, and countries
  • Effectively communicate regulatory changes to the business to maintain compliance and support continuous improvement
  • Lead a team of direct reports, managing resource allocation and assigned projects
  • Provide training and mentoring to new staff
  • Support team with development and innovation

Target Your Resume for "Senior Manager - Submission Management" , Bristol-Myers Squibb

Get personalized recommendations to optimize your resume specifically for Senior Manager - Submission Management. Takes only 15 seconds!

AI-powered keyword optimization
Skills matching & gap analysis
Experience alignment suggestions

Check Your ATS Score for "Senior Manager - Submission Management" , Bristol-Myers Squibb

Find out how well your resume matches this job's requirements. Get comprehensive analysis including ATS compatibility, keyword matching, skill gaps, and personalized recommendations.

ATS compatibility check
Keyword optimization analysis
Skill matching & gap identification
Format & readability score

Tags & Categories

PharmaceuticalPharmaceuticalHealthcare

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