Sr Manager, Line Manager, CDM at Bristol-Myers Squibb

Warsaw, Masovian Voivodeship, Poland

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, BiotechnologyIndustries

Requirements

Leadership experience in clinical data management, including program leadership and potential line management responsibility
Ability to report into Associate Director/Director/Sr. Director level
Full-time office-based with flexibility to work remotely up to 50% of the time over 2 weeks
Strong interpersonal and influencing skills to foster partnerships across global and/or multidisciplinary teams
Knowledge of data management processes to evaluate and recommend new technologies and systems

Responsibilities

Line management of Data Management Data Review staff based on business requirements
Manage resource assignments to ensure appropriate support for data quality oversight in clinical trials
Forecast future resource needs based on book of work and initiatives; propose solutions for resource constraints
Assign resources to initiatives aligned with development plans; provide guidance to drive results
Work with staff to understand strengths, opportunities, and career goals; support development plans and provide regular feedback
Coach and mentor staff, seek training opportunities, and develop next generation leaders
Develop and promote a workplace culture valuing diversity, integrity, accountability, effective decision making, and growth opportunities
Manage and lead clinical data review team, focusing on development, accountability, and success of team members
Contribute to resource allocation decisions for best fit work assignments
Share lessons learned on people management or processes
Act as key point of contact for clinical data review activities during study start up, conduct, and closeout phases
Contribute to clinical data review and overall CDM process optimization and improvement
Act as core member of study team; provide FSP/CRO/Vendor oversight for end-to-end Data Management activities (primarily clinical data review), manage data currency, and monitor DM deliverables per SLA
Support change management initiatives with broad impact as lead or participant; author or participate in functional SOPs/WP/GD
Utilize knowledge of data management processes to evaluate and recommend new technologies and systems
Mentor new or existing team members as applicable
Lead CAPA management activities and ensure timely closure of CAPA action items

Skills

Key technologies and capabilities for this role

Clinical Data ManagementData ReviewLine ManagementResource ForecastingStaff DevelopmentClinical TrialsData Quality Oversight

Questions & Answers

Common questions about this position

What is the work arrangement for this position?

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

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.

What leadership responsibilities does this role involve?

The role includes line management of Data Management Data Review staff, resource forecasting and assignment, coaching and mentoring staff, and developing a workplace culture that values diversity, integrity, and growth.

What is the company culture like at Bristol Myers Squibb?

The culture emphasizes challenging, meaningful, and life-changing work alongside high-achieving teams, with a focus on growth opportunities, balance, flexibility, and developing a workplace that values diversity of thought, integrity, accountability, and effective decision making.

What makes a strong candidate for this Sr Manager role?

Strong candidates will have leadership experience in clinical data management, skills in line management, resource forecasting, coaching, mentoring, and leveraging interpersonal skills to foster partnerships across global teams.

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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