Senior Specialist, Submission Management

Posted 2 Days Ago
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Hyderabad, Telangana
In-Office
Mid level
Healthtech
The Role
The Senior Specialist manages submission documents for health authorities, ensuring compliance and accuracy while interacting with stakeholders and coordinating projects.
Summary Generated by Built In

Working with Us
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams. Take your career farther than you thought possible.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us.

Responsibilities

  • The Senior Specialist manages and coordinates the timely, compliant, and accurate delivery of submission documents and dossiers to health authorities. 

  • Tracks, collects, and reviews all components for submission to Health Authorities. 

  • Interacts with responsible parties for quality submission documents for submissions. 

  • Facilitate submission team meetings with team support. 

  • May participate in focused projects related to their scope of work. 

  • Prepare Cover Letter, FDA Forms and submission content plan for Investigational, Marketed Applications submissions (CSR, Variations, DSURs, PSURs, Initial IND Submission). 

  • Attend Submission Team and kick off meetings, represent RISM and drive submission publishing timelines. 

  • Coordinate Initial IND Kick off meeting submission. 

  • Coordinate IND, NDA, BLA and Orphan Drug Annual Reports. 

  • Develop/Update job aid documents for departmental process. 

  • Build/Manage CARA/PRISM Structures for Global CMC Submissions (CMC Submission Specialist). 

  • Coordinate non-eCTD submissions with International Regulatory Team lead. 

Experience & Key Competency Requirements

  • 3+ years relevant submissions experience

  • Foundational knowledge of global regulatory practices, submission guidelines and requirements.

  • Assists in the implementation of short- and long-term goals within own work group within RISM.

  • Come prepared with a solution to questions and issues as they arise.

  • Engages relevant stakeholders to help address the problem.

  • • Proficient in the English language both written and oral, and able to communicate effectively in written form with non-English speakers.

  • Demonstrates basic presentation skills needed to deliver content to a variety of audiences.

  • Demonstrates the ability to execute a non-complex project, including the ability to prioritize tasks with strong attention to detail.

  • Communicates project status and updates, as appropriate, to relevant stakeholders.

  • Applies critical thinking skills to daily workload decisions, in alignment with group/company objectives.

  • Proposes alternative solutions for submission-related and/or project situations.

  • Seeks to understand stakeholder needs, priorities, working processes, and activities.

  • Good understanding of desktop application software suites.

  • Knowledge and some experience of computer systems in an R&D environment.

Degree Requirements

  • BA/BS degree, science / technology field preferred.

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has an occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

Supporting People with Disabilities

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

Candidate Rights

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Data Protection

We will never request payments, financial information, or social security numbers during our application or recruitment process. Learn more about protecting yourself at https://careers.bms.com/fraud-protection.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

Top Skills

Desktop Application Software Suites
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The Company
HQ: Lawrence Township, NJ
40,384 Employees

What We Do

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. That work inspires some of the most interesting, meaningful, and life-changing careers you’ll experience. Join us and pursue innovative ideas alongside some of the brightest minds in biopharma, collaborating with a team rich in diversity of experiences, and perspectives. We have built a sustainable pipeline of potential therapies and are leveraging translational medicine and data analytics to understand how we can deliver the right medicine to the right patient, at the right time, to achieve the best outcome.

Whether in a scientific, business or supporting function, a career at BMS means you’ll be inspired every day to grow and thrive through opportunities that are uncommon in scale and scope. Here, you’ll be on the cutting edge of powerful innovation in oncology, hematology, immunology, cardiovascular disease, and fibrosis, with colleagues united in the mission to help patients.

Through the Bristol Myers Squibb Foundation, we also promote health equity and seek to improve health outcomes of populations disproportionately affected by serious diseases and conditions. Our mission is to give new hope to help patients prevail over serious disease – it drives everything we do.

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