Remote Clinical Research Associate — Impactful Trials

Bristol Myers Squibb; United States; Hybrid; USD 85,000 - 110,000; Full time

Job summary

Bristol Myers Squibb is seeking a Clinical Research Associate (CRA) to oversee site monitoring and ensure data integrity across trials in the United States. This role focuses on site qualification, initiation, monitoring, and close-out activities in alignment with ICH GCP, SOPs, and regulatory requirements.

The successful candidate will support cross-functional teams, maintain patient safety standards, and contribute to audits and inspections, while advancing trials with a focus on quality and

Qualifications

• Knowledge of clinical research processes, regulations and methodologies.
• Ability to work independently with strong attention to detail.
• Strong communication skills in English (verbal and written).
• Experience with ICH/GCP guidelines and regulatory requirements.

Responsibilities

• Perform site qualification, initiation, monitoring and close-out visits per protocol and Site Monitoring Plan.
• Ensure data accuracy and integrity across electronic and paper records.
• Coordinate with internal and external stakeholders to maintain study progress and safety.
• Support sponsor audits and health authority inspections as needed.
• Develop and deliver timely reports for site performance and study status.

Skills

Clinical research knowledge

Data integrity

Communication in English

Analytical thinking

Autonomy

Time management

Education

Bachelor’s degree in life sciences

Tools

CTMS

eDC

eTMF

RBQM

Job description

Bristol Myers Squibb is seeking a Clinical Research Associate (CRA) to oversee site monitoring and ensure data integrity across trials in the United States. This role focuses on site qualification, initiation, monitoring, and close-out activities in alignment with ICH GCP, SOPs, and regulatory requirements.

The successful candidate will support cross-functional teams, maintain patient safety standards, and contribute to audits and inspections, while advancing trials with a focus on quality and