Senior Clinical Trials Monitor (Remote) — Site Leadership

Parexel; Concord (NH); Remote; USD 90,000 - 120,000; Full time

Job summary

Parexel is seeking a Senior Clinical Research Associate to manage investigator sites, monitor trials, and ensure high-quality study execution in line with GCP and sponsor standards.

The Sr. CRA will lead site activation through database lock, maintain strong site relationships, and coordinate with the SCP and study team to address risks and ensure patient safety while supporting recruitment and timely data delivery.

Qualifications

• Bachelor’s degree in life sciences or related field.
• 2+ years of site monitoring experience.
• Fluency in English and local language(s).
• Ability to travel 60-80%.
• Valid driver’s license and passport.

Responsibilities

• Ensure proper conduct of clinical trials in accordance with SMP, laws, GCP, and sponsor standards to meet goals.
• Manage site activation through database lock, ensuring timelines and quality deliverables.
• Serve as primary contact for investigator sites; coordinate with Site Care Partner.
• Interface with study team, vendors, and sites to facilitate information flow.
• Coach investigator site staff to ensure protocol compliance and patient safety.
• Attend investigator meetings; support recruitment and activation at the site level.
• Conduct onsite/remote monitoring per SMP and SOPs.
• Monitor AEs/SAEs and follow up to resolution with the Drug Safety Unit.
• Submit TMF documentation, site reports, deviations, recruitment, and progress metrics.
• Identify and resolve site issues; develop corrective/preventive actions (CAPA).
• Prepare investigator site close-out plans and execute close-out activities.

Skills

Clinical trial monitoring

GCP/regulatory knowledge

Fluent English & local language

Travel 60-80%

Driver’s license & passport

Education

Bachelor’s degree in life sciences

Job description

Parexel is seeking a Senior Clinical Research Associate to manage investigator sites, monitor trials, and ensure high-quality study execution in line with GCP and sponsor standards.

The Sr. CRA will lead site activation through database lock, maintain strong site relationships, and coordinate with the SCP and study team to address risks and ensure patient safety while supporting recruitment and timely data delivery.