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    Manager, Clinical And Safety Analytics

    Bristol Myers Squibb
    5+ years
    Not Disclosed
    Hyderabad
    10 Sept. 26, 2024
    Job Description
    Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

    Job Opportunity: Manager, Clinical and Safety Analytics at Bristol Myers Squibb

    About Us:

    At Bristol Myers Squibb, we are committed to transforming patients’ lives through innovative science. We offer an environment where meaningful work happens daily across all departments, from groundbreaking production processes to advancements in cell therapy. Join us and take your career further than you ever thought possible, surrounded by diverse and high-achieving teams.

    We prioritize balance and flexibility, offering competitive benefits and resources to support your goals both professionally and personally. Discover more about us at careers.bms.com/working-with-us.

    Position Summary:

    The Manager, Clinical and Safety Analytics will be a pivotal member of the Pharmacovigilance (PV) Analytics Center of Excellence (CoE). This role involves gathering stakeholder requirements, analyzing data, developing visualizations and dashboards, generating insights, and effectively communicating these findings to stakeholders.

    Key Responsibilities:

    • Collaborate closely with cross-functional teams, including clinical and safety stakeholders, to understand their needs and develop analytical solutions.
    • Perform data cleaning, transformation, and other engineering tasks to ensure high data quality and compatibility for analysis.
    • Develop and implement data analysis plans to address inquiries from clinical and safety teams.
    • Utilize analytical and statistical techniques to analyze data and generate insights that inform clinical and safety questions.
    • Create effective, user-friendly dashboards and visualizations to address key clinical, safety, and regulatory inquiries.
    • Communicate insights clearly to both technical and non-technical stakeholders, ensuring a shared understanding of the data.
    • Contribute to qualitative and quantitative research projects in collaboration with teams such as Pharmacovigilance, Epidemiology, and Biostatistics.
    • Stay updated on new tools and technologies, assessing analytics and data visualization platforms for potential improvements.
    • Serve as a subject matter expert on analytics and business intelligence, sharing best practices with the organization.

    Skills & Competencies:

    • Strong understanding of data sources, including clinical trial data and electronic health records.
    • Proficiency in data preprocessing, cleaning, and transformation techniques.
    • Knowledge of analytical methodologies, including regression and survival analysis.
    • Excellent problem-solving skills with the ability to extract meaningful insights from complex data sets.
    • Strong communication and presentation skills to convey complex findings effectively.
    • Ability to work collaboratively in cross-functional teams while managing multiple projects.
    • High attention to detail and accuracy in data analysis.

    Experience:

    • Bachelor’s or Master’s degree in a relevant field (e.g., Biostatistics, Analytics, Engineering).
    • Minimum of 5+ years of experience in data analysis, statistical modeling, or data visualization, ideally in the biopharma or healthcare sector.
    • Proven experience applying statistical techniques to analyze clinical and real-world datasets.
    • Familiarity with programming languages such as Python, R, or SAS, and SQL.
    • Experience with visualization tools, especially Tableau (preferred), or Power BI.
    • Background in the biopharma industry is a plus.

    Join Us:

    If you're excited about the opportunity to make a difference in patients’ lives and contribute to life-changing work, we encourage you to apply—even if your experience doesn't perfectly match the job description. You might be just one step away from an incredible career at Bristol Myers Squibb.

    Work Environment:

    Bristol Myers Squibb offers a diverse occupancy structure, which includes site-essential, site-by-design, field-based, and remote-by-design roles. Your assigned occupancy type will depend on the nature of your role.

    BMS is committed to creating an inclusive environment. We encourage applicants who may require accommodations during the recruitment process to reach out to adastaffingsupport@bms.com.

    We prioritize the health and well-being of our employees and the communities we serve. As such, we strongly recommend that all employees are fully vaccinated for COVID-19 and remain up to date with boosters.

    Bristol Myers Squibb is an equal opportunity employer. We welcome applications from qualified individuals, including those with arrest and conviction records, in accordance with applicable laws.

    Your Journey Begins Here:

    We value your privacy and are committed to protecting your personal information throughout the recruitment process. All data will be processed in line with applicable data privacy policies and regulations.

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