Clinical Scientist at Bristol-Myers Squibb

Warsaw, Masovian Voivodeship, Poland

Bristol-Myers Squibb Logo
Not SpecifiedCompensation
Mid-level (3 to 4 years)Experience Level
Full TimeJob Type
UnknownVisa
Pharmaceuticals, Biotechnology, Clinical ResearchIndustries

Requirements

  • Degree in Life Sciences (MD, PhD, Pharm D, MS, RN or similar scientific field preferred)
  • 2+ years of experience in clinical science, clinical research, or equivalent
  • Proficient knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations
  • Ability to understand assigned protocol(s) and their requirements
  • Knowledge and skills to support program-specific data review and trend identification
  • Intermediate medical writing skills and medical terminology
  • Basic knowledge of the establishment and operation of data monitoring committees, dose review teams, and independent response adjudication committees
  • Basic planning/project management skills (develop short range plans that are realistic and effective)
  • Basic knowledge of disease area, compound, current clinical landscape
  • Detail-oriented with commitment to quality
  • Intermediate critical thinking and problem-solving skills
  • Adaptable / flexible (willing and able to adjust to multiple demands and shifting priorities; ability to meet day-to-day challenges with confidence and professionalism)
  • Intermediate skills in Microsoft Word/Excel/PowerPoint and data review tools (e.g., patient profiles, report generating tools)
  • Willingness to travel domestically and internationally (10 - 25%)

Responsibilities

  • Collaborate and liaise with external partners (e.g., KOLs)
  • Seek out and enact best practices with instruction
  • Provide regular and timely updates to manager/management as requested
  • Collaborate cross-functionally to develop Protocol and ICF documents / amendments and present these to governance committee and early clinical development team meetings as required
  • Conduct literature review
  • Develop site and CRA training materials and present these at SIVs and Investigator meetings
  • Review clinical narratives
  • Collaborate cross-functionally to monitor clinical data for specific trends
  • Contribute to the development of Data Review Plan in collaboration with Data Management
  • Ensure CRF design adequately supports data collection in alignment with the protocol in collaboration with Data Management/Programming
  • Author/review clinical contributions to clinical study reports (CSRs) and clinical portions of Regulatory Documents (e.g., Pre-IND, IND, IB, DSUR, PSUR, Orphan Annual Reports, HA, EC, IRB responses and contribute to regulatory submission)
  • Submit clinical documents to TMF
  • Design and execution of assigned clinical trial activities and works closely with clinical team members to execute activities associated with trial conduct
  • May lead or support trial level activities for one or more trials with the necessary supervision

Skills

Key technologies and capabilities for this role

Clinical Trial DesignProtocol DevelopmentInformed Consent FormsLiterature ReviewSite TrainingCRA TrainingData MonitoringData Review PlanCRF DesignKOL Collaboration

Questions & Answers

Common questions about this position

What benefits does Bristol Myers Squibb offer?

Bristol Myers Squibb offers a wide variety of competitive benefits, services, and programs that provide employees with resources to pursue their goals both at work and in their personal lives.

Is this a remote position or does it require office work?

This information is not specified in the job description.

What salary can I expect for the Clinical Scientist role?

This information is not specified in the job description.

What key skills are required for the Clinical Scientist position?

Required skills include basic planning and project management, intermediate critical thinking and problem-solving, adaptability and flexibility, detail-orientation with commitment to quality, and intermediate skills in Microsoft Word, Excel, PowerPoint, and data review tools.

What is the company culture like at Bristol Myers Squibb?

The culture emphasizes challenging, meaningful, and life-changing work in a flexible environment with high-achieving teams, opportunities for growth, and a focus on work-life balance.

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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