Remote CRA II/Senior — Metabolic & Obesity Trials

Parexel; Salem (OR); Remote; USD 70,000 - 90,000; Full time

Benefits offered by this job

Health, Vision & Dental Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

401(k) with Company match

Pet Insurance

Job summary

Parexel, a leading global clinical development partner, is seeking a Clinical Research Associate with Metabolic/MASH or Obesity monitoring experience to join our team in Salem, Oregon. You will manage clinical sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data.

You will conduct onsite monitoring, build productive site relationships, address issues, and support enrollment and study delivery.

Qualifications

• 18+ months of direct onsite monitoring experience as a CRA.
• Metabolic/MASH and/or Obesity trial monitoring experience.
• Bachelor's degree or equivalent in a health-related discipline.
• Knowledge of GCP and regulatory requirements.
• Experience using CTMS, EDMS and MS Office.
• 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 help safeguard the rights, safety, and well-being of study participants in accordance with the protocol.
• Develop patient recruitment strategies with clinical sites to support enrollment timelines.
• Ensure compliance with approved SOPs, study protocols and amendments, Good Clinical Practice, and regulatory requirements.
• Evaluate the quality and integrity of reported data, site performance, and investigational product accountability.
• Monitor the completeness and quality of regulatory documentation and perform site document verification.

Skills

Site relationship management

Problem-solving

Communication skills

Independent work

Time management

Ethical patient-focused

Cross-functional collaboration

Education

Bachelor's degree in biological sciences

Equivalent health-related discipline

Tools

CTMS

EDMS

Excel

Word

MS Office

Job description

Parexel, a leading global clinical development partner, is seeking a Clinical Research Associate with Metabolic/MASH or Obesity monitoring experience to join our team in Salem, Oregon. You will manage clinical sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data.

You will conduct onsite monitoring, build productive site relationships, address issues, and support enrollment and study delivery.