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Associate Director, SDTM Programming

Associate Director, SDTM Programming

Bristol Myers Squibb

10 - 15 years

20 - 27 Lacs

Hyderabad

Posted:3 hours ago| Platform:

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Skills Required

Computer science Statistical programming Internal audit Pharma Clinical trials clinical development Issue resolution data privacy Analytics clinical data

Work Mode

Work from Office

Job Type

Full Time

Job Description

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.

Duties/Responsibilities

Lead/actively participate in departmental and/or cross-functional initiatives geared towards updated technological solutions, process improvements, standards and governance updates etc. and regularly disseminate information to teams and stakeholders.
Drive forward a lean SDTM implementation group capable of delivering quality SDTM data early in a clinical trial with innovative transformation solutions.
Keep abreast of CDISC industry standards and participate in industry wide technical discussions via conferences and webinars.
Represent SDTM programming during internal audits as needed.

Managerial Responsibilities:

Develop job descriptions and career paths for programmers and effectively forecast resource needs, recruit, manage, develop, evaluate, reward, motivate and retain direct reports, resulting in an increasing level of capabilities within GBDS.
Conducts objective setting, performance check-ins, and year-end discussions in compliance with BMS policies.
Aligns objectives, feedback and performance evaluation with direct manager.
Meets regularly with direct reports, focusing on project updates, development needs, issue resolution, and provides real-time coaching and feedback.
Holds staff accountable for quality and timeliness of programming activities; ensures staff is compliant with training requirements
Communicates with Head of Clinical Data Strategy, Systems, Reporting and Analytics regarding promotions, performance concerns, and retention risks.
Build inter-departmental relationships and resolve issues as needed.

Qualifications

Graduate degree in statistics, biostatistics, mathematics, computer science or equivalent experience preferred. Minimum of 10 years clinical/statistical programming experience within pharmaceutical clinical development.

Minimum 5 years of experience in managing technical professionals in a regulated environment.

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.

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:

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Bristol Myers Squibb

Pharmaceutical Manufacturing

Lawrence Township NJ

10001 Employees

185 Jobs

Key People

Giovanni Caforio

Chairman and CEO
Rupert Vessey

Executive Vice President, Chief Medical Officer
David Elkins

Executive Vice President, Head of Global Commercialization
Maggie O'Neill

Senior Vice President, Human Resources

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Associate Director, SDTM Programming