Clinical Research Associate at Bristol-Myers Squibb

Budapest, Budapest, Hungary

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Biotechnology, Clinical ResearchIndustries

Requirements

Understanding and proficiency working with targeted, centralized, remote and risk-based monitoring approaches
Strong analytical skills to evaluate site data and operational metrics, including ability to adjust monitoring strategies based on data trends and site performance
Effective communication skills, adapting to meet the needs of different stakeholders, utilizing the most appropriate communication style and method
Ability to assess potential Investigators and their sites to ensure sufficient resources and capabilities to conduct clinical trials
Knowledge of ICH GCP, local regulations, protocol, BMS SOPs, and principles of ALCOA for data integrity

Responsibilities

Conduct site qualification, initiation, routine monitoring and close-out visits across all trial phases in accordance with the Site Monitoring Plan, ensuring adherence to protocol, BMS SOPs and ICH GCP
Maintain the ethical and scientific integrity of clinical trials by verifying data within electronic systems and paper records to ensure accessibility, completeness and accuracy
Monitor site adherence to ICH GCP and local regulations, including compliance with ALCOA principles; provide training and support to site staff to uphold standards and ensure patient safety
Participate in sponsor and/or Health Authority audits and inspections as applicable
Cultivate and sustain effective relationships with internal cross-functional teams and external partners, including vendors, clinical sites, and key stakeholders; serve as the organization’s representative at the site level
Motivate and influence sites to meet study objectives, including enrollment and retention goals
Prepare and submit written reports, both monitoring and administrative, in a timely, accurate, concise, professional and objective manner
Identify new potential Investigators and/or sites through ongoing collaborations during the site feasibility and selection process
Identify, assess, and prioritize risks at the site and study level; support sites in mitigating issues and implementing mitigation strategies based on risk indicators
Where applicable, perform Unblinded Site Monitor activities to protect the blind of the study by acting as secondary monitoring

Skills

Key technologies and capabilities for this role

ICH GCPSite MonitoringClinical Trial ManagementProtocol AdherenceSOPsSite QualificationSite InitiationRoutine MonitoringSite Close-outData Verification

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 travel?

This information is not specified in the job description.

What are the key responsibilities of a Clinical Research Associate at BMS?

Key responsibilities include conducting site qualification, initiation, routine monitoring and close-out visits, maintaining data integrity, monitoring adherence to ICH GCP and regulations, building relationships with stakeholders, and preparing monitoring reports.

What is the company culture like at Bristol Myers Squibb?

The culture is described as challenging, meaningful, and life-changing, with uniquely interesting work, opportunities to grow alongside high-achieving teams, and a focus on work-life balance and flexibility.

What makes a strong candidate for the CRA role?

Strong candidates should have experience in clinical trial monitoring, knowledge of ICH GCP, SOPs, and regulations, strong relationship-building skills, and the ability to ensure data integrity and site compliance.

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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