Associate Director, Clinical Biomarker Neuro-Immunology, Late Stage Translational Development at Bristol-Myers Squibb

Princeton, New Jersey, United States

Bristol-Myers Squibb Logo
Not SpecifiedCompensation
Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, BiotechnologyIndustries

Requirements

  • Recognized expertise in translational biomarkers in neuroimmunology
  • Experience in late-stage drug development activities related to clinical trial initiation, maintenance, and completion
  • Strong verbal and written communication skills
  • Experience in interacting with CROs and TLs to manage projects and timelines
  • Proven scientific/leadership expertise (working in teams, mentoring people, managing projects)
  • Accountable for timelines and deliverables
  • Prioritizes risks and implements contingency plans
  • Communicates regularly and prepares presentations

Responsibilities

  • Designs and implements program-specific late development biomarker/translational plans
  • Creates clinical protocols, SAPs, SOWs, lab manuals, and interfaces with CROs for service execution
  • Determines appropriate assays and vendors for clinical biomarkers and manages outsourcing
  • Manages clinical biomarker data delivery and analysis, working with internal functions and CROs
  • Prepares and delivers internal and external translational/biomarker presentations
  • Maintains timelines for biomarker data related to publication, collaborating with Medical Communications and Publication teams
  • Keeps up-to-date on relevant scientific/technical literature and applies external knowledge to internal research programs
  • Works with TM laboratory scientists and academic TLs to address nonclinical translational questions
  • Participates in post-hoc biomarker analysis and publication efforts
  • Supports regulatory submissions and interactions as needed

Skills

neuroimmunology
translational biomarkers
clinical protocols
SAPs
SOWs
lab manuals
CRO management
biomarker assays
data analysis
scientific presentations
project management
regulatory submissions

Bristol-Myers Squibb

Develops and delivers biopharmaceutical medicines

About Bristol-Myers Squibb

Bristol Myers Squibb (BMS) develops and delivers medicines aimed at treating serious diseases, focusing on areas like cancer, autoimmune diseases, and heart conditions. The company conducts extensive research and development to create new drugs, which are sold after receiving regulatory approval. BMS also produces generic drugs, offering affordable alternatives that meet the same quality standards as their branded counterparts. What sets BMS apart from competitors is its dual focus on both innovative and generic medicines, enhancing access to healthcare. The company's goal is to improve patient outcomes while maintaining a commitment to sustainability and corporate responsibility.

New York City, New YorkHeadquarters
1887Year Founded
$33,706.1MTotal Funding
IPOCompany Stage
Biotechnology, HealthcareIndustries
10,001+Employees

Benefits

Flexible Work Hours
Hybrid Work Options
Professional Development Budget

Risks

Increased competition in oncology from emerging biotech firms like ArsenalBio.
BMS's lawsuit over the 340B Drug Pricing Program may lead to regulatory challenges.
Rapid AI and digital tech evolution may pose integration challenges for BMS.

Differentiation

BMS focuses on innovative cancer treatments through collaborations like ArsenalBio for T cell therapies.
The company emphasizes digital health technologies, enhancing clinical trial management and patient engagement.
BMS offers both innovative and generic medicines, increasing affordable healthcare solutions.

Upsides

BMS's partnership with Medidata enhances clinical research processes and patient outcomes.
The collaboration with AI Proteins advances novel miniprotein-based therapeutics, expanding therapeutic modalities.
BMS's global license agreement with BioArctic expands its portfolio in neurodegenerative diseases.

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