Senior Clinical Site Monitor — Global Trials

Regulatory Jobs; Tempe (AZ); On-site; USD 90,000 - 150,000; Full time

Job summary

BD, a leading global medical technology company, seeks a Clinical Site Monitoring professional to ensure compliance and quality across BDPI studies in the United States, including Tempe. You will manage on-site and remote monitoring activities, collaborate with cross-functional teams, and support regulatory and documentation processes.

The role requires 3+ years in clinical research, knowledge of GCP/ISO14155, and the ability to travel up to 60%. A BS/BA in life sciences is preferred.

Qualifications

• Knowledge of domestic and international clinical research regulations and guidelines (GCP/ICH, ISO14155).
• Proficiency with Microsoft Suite tools (Outlook, Word, Excel, PowerPoint).
• Strong interpersonal, communication, and organizational skills.

Responsibilities

• Provide site management and monitoring support for BDPI clinical studies to enable study objectives and deliverables.
• Ensure quality and compliance for clinical studies at sites, adhering to BD procedures and regulatory requirements.
• Conduct on-site or remote monitoring activities, screen sites, review informed consent, data queries, and regulatory approvals.
• Develop and maintain study-specific tracking reports to detail progress and timelines.
• Perform TMF audits and support CTMS/data management activities.
• Mentor and oversee site management personnel and contribute to process improvements.

Skills

Regulatory knowledge

GCP/ISO14155

MS Office

Communication skills

Travel up to 60%

Education

Bachelor’s Degree (BS/BA) in life sciences

Tools

Veeva Vault CTMS

CDMS

eTMF

Job description

BD, a leading global medical technology company, seeks a Clinical Site Monitoring professional to ensure compliance and quality across BDPI studies in the United States, including Tempe. You will manage on-site and remote monitoring activities, collaborate with cross-functional teams, and support regulatory and documentation processes.

The role requires 3+ years in clinical research, knowledge of GCP/ISO14155, and the ability to travel up to 60%. A BS/BA in life sciences is preferred.