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Bristol Myers Squibb - Manager - Biospecimen

Bristol Myers Squibb - Manager - Biospecimen

Bristol Myers SquibbHyderabad, India
1 day ago
Job description

Manager - Biospecimen 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 .

Position Summary :

  • We are seeking a candidate with knowledge of clinical trials and the end-to-end management of biospecimens.
  • You will be an independent contributor who will work closely with our Clinical Teams to develop and implement biospecimen management plan for BMS-sponsored Phase 1-4 clinical trials.
  • Critical to this role is the ability to oversee timelines for specimen data delivery and thereby, enabling quick decision-making and ensuring BMS's continuous competitive advantage.
  • Key Responsibilities :

  • Oversee and manage the complete lifecycle of biospecimens collected for clinical studies with minimal supervision.
  • Clinical Team member responsible for providing shipping / sample movement and management including requests, query and inventory reports, follow up active issues with vendors, prepare sample management related reports, review / prepare tracking activities (such as vendor manifests / inventories, tissue / blood match pairing, depleted / non-viable samples, loading documents to Shared Drive folders, etc.
  • Independently reviews clinical study protocol providing comparison of vendor statement of work and biospecimen relevant sections and feedback with support as needed.
  • Performs routine vendor management responsibilities.
  • Able to request and / or access necessary vendor / system inventory files to perform specimen tracking.
  • Able, under direction, to create biospecimen tracker using various tracking tools (MS Excel, Spotfire, Tableau or internal systems (if applicable)).
  • Exercises judgment within policy and procedure boundaries.
  • Troubleshoots routine problems and understands when appropriate to ask for guidance.
  • Qualifications & Experience :

  • Minimum of 3-4 years academic, biotech, healthcare or pharmaceutical industry experience or equivalent.
  • Basic understanding of clinical and biomedical research, GCP, GLP, CLIA, data management, risk management and regulatory issues.
  • Demonstrated clinical trial experience, healthcare / medical / laboratory or equivalent.
  • Vendor experience preferred (e.g., Central Labs, Bioanalytical, Biomarker, CROs, Biospecimen Storage Vendors, etc.
  • Biospecimen management experience preferred but not mandatory.
  • Ability to effectively communicate, create and deliver presentation / information / data to knowledgeable audiences, with limited supervision.
  • Ability to adopt a biopharma enterprise-wide and entrepreneurial mindset, to act with a sense of urgency, accountability and integrity, and to have fun along the way.
  • Travel requirement is minimal, 0%5% of time, when organization requests.
  • 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 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.
  • 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.
  • 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.
  • (ref : iimjobs.com)

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