Clinical Data Manager 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, HealthcareIndustries

Requirements

  • Bachelor’s Degree required. Life sciences, Pharmacy or relevant fields preferred
  • 2 years of experience in Clinical Data Review tasks
  • Able to work on clinical data review tasks
  • Able to work collaboratively on multi-disciplinary project teams
  • Basic knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management
  • Good knowledge and experience of EDC systems (Medidata RAVE preferred); demonstrated knowledge of Microsoft Office skills
  • Good oral and written communication skills
  • Able to travel 5-10% for Industry Conferences, Investigator Meetings, Regulatory Inspections (as needed)

Responsibilities

  • Understand and review Protocol along with relevant data review documents (e.g. Protocol Data Review Plan, Data Quality Management Plan)
  • Review clinical data listings
  • Manage and facilitate resolution of data discrepancies
  • Perform data cleaning as per the defined Clean Patient Group
  • Freezing & Locking of CRFs/Fields
  • Coordinate with Data Management Lead for study deliverables
  • Complete review of loaded external data
  • Track data load and address discrepancies
  • Coordinate with external data vendor for resolution of data discrepancies as applicable
  • Filing of appropriate documents in eTMF as per eTMF master plan

Skills

Key technologies and capabilities for this role

Clinical Data ManagementData ReviewData CleaningCRF FreezingData Discrepancy ResolutionExternal Data ReviewProtocol ReviewData Quality Management

Questions & Answers

Common questions about this position

What is the work arrangement for this Clinical Data Manager role?

This is a full-time office-based position with flexibility to work remotely up to 50% of the time over 2 weeks.

What experience and education are required for this position?

A Bachelor’s Degree is required, preferably in life sciences, pharmacy, or relevant fields, along with 2 years of experience in Clinical Data Review tasks.

What are the main responsibilities of the Clinical Data Manager?

Responsibilities include data review such as reviewing protocol and data listings, managing data discrepancies, freezing and locking CRFs, handling external data, and filing documents in eTMF.

What is the company culture like at Bristol Myers Squibb?

The culture emphasizes challenging, meaningful, and life-changing work that transforms patients' lives and careers, with opportunities to grow alongside high-achieving teams, and a focus on balance and flexibility.

What travel is required for this role?

Travel is required at 5-10% for industry conferences, investigator meetings, and regulatory inspections as needed.

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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