Senior Clinical Site Monitor - MedTech Research

Becton, Dickinson and Company; Tempe (AZ); On-site; USD 110,000 - 140,000; Full time

Job summary

BD in Tempe, AZ is seeking a Clinical Site Management & Monitoring professional to independently manage BDPI clinical studies, ensuring scientific quality and adherence to GCP, ISO14155 and regulatory standards.

You will conduct on-site and remote monitoring, review informed consent, track study progress, and collaborate with BD stakeholders to ensure timely, compliant study deliverables and strong site partnerships across cross-functional teams.

Qualifications

• Knowledge of domestic and international clinical research regulations and guidelines.
• Proficiency with Microsoft Suite tools.
• Strong knowledge of clinical study processes and systems (eTMF, CTMS and CDMS).

Responsibilities

• Independently Provide Site Management & Monitoring support for BDPI clinical studies to enable successful completion of study objectives and deliverables.
• Ensure quality and compliance for assigned clinical studies and study activities performed at assigned clinical sites, ensuring the highest standards for scientific quality, integrity and ethics are met and that these are conducted in accordance with BD global clinical procedures, study protocols, GCP and all applicable regulations.
• Escalates & address non-compliance issues. Communicates and collaborates w/ study leadership.
• Develop and maintain strong relationships as the primary site contact.

Skills

Clinical monitoring

GCP/ICH knowledge

GDP/GCP practices

Regulatory knowledge

Microsoft Office

Cross-functional collaboration

Education

Bachelor's Degree in life sciences

MA/MS preferred

Tools

eTMF

CTMS

CDMS

Veeva Vault CTMS

Job description

BD in Tempe, AZ is seeking a Clinical Site Management & Monitoring professional to independently manage BDPI clinical studies, ensuring scientific quality and adherence to GCP, ISO14155 and regulatory standards.

You will conduct on-site and remote monitoring, review informed consent, track study progress, and collaborate with BD stakeholders to ensure timely, compliant study deliverables and strong site partnerships across cross-functional teams.