Senior CRA - Metabolic Trials (Remote)

Parexel; Montpelier (VT); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health insurance

Tuition reimbursement

Vacation/holiday/sick time

Flexible Spending Accounts

Work/Life Balance

401(k) with company match

Pet insurance

Job summary

Parexel is seeking a Clinical Research Associate with Metabolic/MASH or Obesity monitoring experience to join our global clinical development team. You will manage sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data, while building strong relationships with investigators and staff.

You’ll conduct onsite monitoring, oversee site performance, support enrollment, and collaborate across therapeutic areas with Parexel’s training

Qualifications

• Onsite monitoring experience in clinical trials.
• Metabolic/MASH or obesity monitoring experience preferred.
• Bachelor's degree or equivalent in a health-related field.
• Knowledge of GCP and regulatory requirements.

Responsibilities

• Conduct qualification visits, SIVs, monitoring visits, and closeout reports.
• Manage site quality and delivery from screening to closeout.
• Serve as primary contact for assigned sites and resolve issues.
• Monitor study integrity and safeguard participant rights and safety.
• Develop patient recruitment strategies with sites to meet timelines.
• Ensure adherence to SOPs, protocols, and regulatory requirements.
• Evaluate data quality and site performance; verify documents.

Skills

Site relationship management

Problem-solving

Communication

Independent work

Client-focused

Education

Bachelor's degree in biological sciences/pharmacy/health

Tools

CTMS

EDMS

MS Office (Excel/Word)

Job description

Parexel is seeking a Clinical Research Associate with Metabolic/MASH or Obesity monitoring experience to join our global clinical development team. You will manage sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data, while building strong relationships with investigators and staff.

You’ll conduct onsite monitoring, oversee site performance, support enrollment, and collaborate across therapeutic areas with Parexel’s training