Manager, Clinical and Safety Analytics

4 weeks ago


Hyderabad, Telangana, India Bristol Myers Squibb Full time
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 rich in diversity. 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: .

BMS Hyderabad is an integrated global hub where our work is focused on helping patients prevail over serious diseases by building sustainable and innovative solutions. This important science, technology, and innovation center will support a range of technology and drug development activities that will help us usher in the next wave of innovation.

Position Summary:

This position is responsible for enhancing and developing a framework related to data analytics reporting utilizing metrics collected within the Worldwide Patient Safety & PV CoE Analytics function. The Analyst will enable analytical use of the compliance data that provides insights related to productivity, efficiency, and quality to facilitate informed decision making for BMS REMS Analytics.

Position Responsibilities
  • Responsible for ensuring compliance with regulatory requirements, enhancing drug safety and regulatory adherence with qualitative and quantitative research projects through collaboration with data trends from cross-functional teams (Regulatory, Medical & Clinical Safety, Commercial, Brand Marketing, etc.)
  • Maintain and develop programming, reporting and analytics applications in BMS environments such as Tableau, Excel.
  • Leverage internal data systems and tools to efficiently maintain data visualization, communications and reporting processes to minimize manual data retrieving.
  • Utilize data analysis tools to aggregate and analyze data to make actional recommendations and answer key business questions.
  • Develop, Run, and maintain reports regarding activities, outcomes, and trends and be prepared to deliver presentations to management team on a regular and ad-hoc basis.
  • Continually remain apprised of the constantly changing landscape of the healthcare industry and any impacts it may have to our REMS programs and reporting mechanisms.
  • Obtain a deep understanding of the prescriber and pharmacy operating environments through View Job Posting Details vendor and consulting interactions, stakeholder discussions, conference attendance, BMS events etc.
  • Analyze key stakeholder complaints, address rapidly, and discuss with applicable functional leads to collaborate and propose impactful and realistic solutions.
  • Interpret and contextualize analytical findings documented by the REMS Advisor team.
Other tasks
  • Provide scheduled and ad-hoc reports to the leadership team as required.
  • Supporting Audit Activities related to BMS REMS programs.
Training & Change Management
  • In partnership with WWPS members, develop and execute change management and change readiness assessments and strategies.
  • Support Stakeholder analysis and mapping, identifying potential impacts/risks Manage efforts related to communication and education of the user community on system progress, objectives, and requirements; and develop means to evaluate and ensure organizational readiness.
  • Contribute to initiatives to develop employees' understanding and acceptance of impacts on specific job roles, policies, technology impacts and business practices.
  • Identify and anticipate organizational challenges and/or resistance; contribute to the development of risk mitigation plans.
  • Plan and Support activities to plan, design, and execute end-user training strategies.
  • Support evaluation of instructional approaches for reports and their requisite systems Conduct and support train-the-trainer workshops as appropriate, related to various reporting applications.
  • Support the review of end-user training materials, job aids and other materials for consistency and relevance in relation to agreed-upon training objectives.
Degree Requirements
  • B S/BA degree required, understanding of FDA Risk Evaluation and Mitigation Strategies (REMS) regulations and at least 4 - 8 years of relevant pharma/biotech experience. Master's or advanced degree preferred.
Key Competency Requirements
  • Strong PowerPoint and Excel Skills
  • Programming languages like SAS, SQL or Python etc.
  • Strong knowledge and expertise in Tableau
  • Databases (Salesforce, Postgres, Oracle, SharePoint List etc.)
  • Ability to organize/curate data and see big picture from scattered pieces of information.
  • Analytical and strategic thinking skills required.
  • Knowledge of Validation processes and associated documentation
  • Excellent verbal, writing, presentation and project management skills
  • Strong strategic orientation with ability to translate into operational priorities and plans.
  • Demonstrated ability to work on multiple projects.
  • Strong willingness to collaborate with cross-functional partners, flexible team member with positive attitude, friendly demeanor, ability to prioritize projects and balance competing priorities.
  • Confidentiality and integrity are required.
  • Strong work ethic a must
#HYDDD #LI-Hybrid

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 scienceTM , 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 an inclusive culture, promoting diversity 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 a diverse 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.

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 . Visit eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

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

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

  • Hyderabad, Telangana, India Luein Analytics Full time

    Summary:As a SAS Clinical Programmer at Luein Analytics, you will play a crucial role in the development and implementation of clinical trial data analysis and reporting. You will be responsible for programming and validating statistical analysis and reporting of clinical trial data using SAS, SQL, MACROS, EXCEL, SDTM, and ADAM. This is a full-time position...

  • Clinical Data Manager

    2 weeks ago


    Hyderabad, Telangana, India Inductive Quotient Analytics Full time

    Position :Clinical Data ManagerRequirement:Immediate JoinerLocation :Hyderabad onlyExperience:5 to 10 Years onlyKey Roles & Responsibilities:Provide leadership and vision to the team.Manage and deliver large-scale, high-complexity studies across a range of sponsors and therapeutic areas.Manage sponsors at both the study and program levels.Ensure milestones...


  • Hyderabad, Telangana, India Inductive Quotient Analytics Full time

    Position: Clinical Data ManagerRequirement: Immediate JoinerLocation: Hyderabad onlyExperience: 5 to 10 Years onlyKey Roles & Responsibilities: Provide leadership and vision to the team. Manage and deliver largescale, highcomplexity studies across a range of sponsors and therapeutic areas. Manage sponsors at both the study and program levels. Ensure...


  • Hyderabad, Telangana, India Bristol-Myers Squibb Full time

    Working with UsChallenging. 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...


  • Hyderabad, Telangana, India Lifelancer Full time

    Job Summary: We are seeking a highly motivated and experienced Clinical Research Associate (CRA) with a minimum of 2-3 years of relevant experience. The CRA will play a critical role in ensuring the successful planning, execution, and monitoring of clinical trials. The ideal candidate will have a strong understanding of clinical trial processes, regulatory...


  • Hyderabad, Telangana, India Thermo Fisher Scientific Full time

    Job DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step...


  • Hyderabad, Telangana, India Thermo Fisher Scientific Full time

    Job DescriptionAt Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step...


  • Hyderabad, Telangana, India Bristol Myers Squibb Full time

    Working with UsChallenging. 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...


  • Hyderabad, Telangana, India Bristol Myers Squibb Full time

    Working with UsChallenging. 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...


  • Hyderabad, Telangana, India UnitedHealth Group Full time

    Optum is a global organization that delivers care, aided by technology to help millions of people live healthier lives. The work you do with our team will directly improve health outcomes by connecting people with the care, pharmacy benefits, data and resources they need to feel their best. Here, you will find a culture guided by diversity and inclusion,...


  • Hyderabad, Telangana, India Oracle Full time

    Job Description `Overview of the Organization Oracle Life Sciences GIU (LSGIU) provides industry leading solution to Life Sciences organizations including pharmaceutical companies, CROs (Contract research Organizations), Academic research and Healthcare providers that include care providers, IDN (integrated delivery networks), public regional/national...


  • Hyderabad, Telangana, India Novartis Full time

    Summary:"150 Clinical scientific experts, globally, are part of Global Drug Development (GDD) team, working to ensure clinical trial data and regulatory reports are of highest quality throughout the life cycle of each program, across all disease areas. Be part of a dedicated, passionate team that is diligently providing clinical and scientific inputs at...


  • Hyderabad, Telangana, India Seven Consultancy Full time

    JOB DETAILS1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...


  • Hyderabad, Telangana, India Seven Consultancy Full time

    JOB DETAILS1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics committee...


  • Hyderabad, Telangana, India Bristol Myers Squibb Full time

    DescriptionCDM is responsible for ensuring the integrity, reliability, completeness, and quality of clinical trial data and provides leadership in clinical data management for trials within the BMS R&D portfolio.Position OverviewThe Senior Clinical Data Manager plays a crucial role in completing data review tasks for assigned studies across different...


  • Hyderabad, Telangana, India Seven Consultancy Full time

    JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...


  • Hyderabad, Telangana, India Seven Consultancy Full time

    JOB DETAILS 1. Ensure that clinical research studies are conducted in accordance with the protocol, standard operating procedures, good clinical practice (GCP) guidelines, and other applicable regulatory requirements.Perform site selection, initiation, monitoring and close-out visits in accordance with contracted scope of work and GCP guidelines.Review...


  • Hyderabad, Telangana, India Seven Consultancy Full time

    JOB DETAILS 1) Creating and writing trial protocols, and presenting these to steering committee.2) Identifying, evaluating and establishing trial sites, and closing sites down on completion of trial.3) Training site staff on therapeutic areas, protocol requirements, proper source documentation and case report form completion.4) Liaise with ethics...


  • Hyderabad, Telangana, India Bristol Myers Squibb Full time

    Working with UsChallenging. 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...


  • Hyderabad, Telangana, India Bristol Myers Squibb Full time

    Working with UsChallenging. 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...