Senior CRA: Metabolic & Obesity Trials (Remote)

Parexel International; United States; Remote; USD 70,000 - 100,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending Account

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with Metabolic/MASH or Obesity monitoring experience to join our team in the United States. You will manage clinical sites from identification through closeout, acting as the primary contact for site teams and ensuring study quality, patient safety, regulatory compliance, and data integrity.

You will conduct onsite monitoring activities, build strong site relationships, support enrollment, and ensure adherence to GCP and approved protocols.

Qualifications

• At least 18 months of direct onsite monitoring experience as a CRA.
• Metabolic/MASH and/or Obesity clinical trial monitoring experience.
• Bachelor's degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of Good Clinical Practice, regulatory requirements, and clinical trial processes.
• Experience using CTMS, EDMS, and MS Office (Excel, Word).
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.

Responsibilities

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned clinical sites, and prepare timely visit and contact reports.
• Manage site quality and delivery from site identification through closeout.
• Serve as the primary point of contact for assigned clinical sites, addressing questions and resolving issues to support successful study execution.
• Oversee study integrity and build effective relationships with investigators and site staff.
• Review trial performance at designated sites and safeguard rights, safety, and well-being of participants.
• Develop patient recruitment strategies with clinical sites to support enrollment timelines.
• Ensure compliance with SOPs, protocols, GCP, and regulatory requirements.
• Evaluate data quality and site performance, and ensure investigational product accountability.
• Monitor completeness and quality of regulatory documentation and perform site document verification.

Skills

Site relationship management

Problem-solving

Communication skills

Independent worker

Client-focused

Time management

Quality focus

Stakeholder communication

Education

Bachelor's degree in biological science or health-related discipline

Tools

Clinical Trial Management System

Electronic Document Management System

Microsoft Excel

Microsoft Word

Job description

Parexel is seeking a Clinical Research Associate (CRA) with Metabolic/MASH or Obesity monitoring experience to join our team in the United States. You will manage clinical sites from identification through closeout, acting as the primary contact for site teams and ensuring study quality, patient safety, regulatory compliance, and data integrity.

You will conduct onsite monitoring activities, build strong site relationships, support enrollment, and ensure adherence to GCP and approved protocols.