Clinical Research Associate: Site Partnerships & Impact

Parexel; Helena (MT); On-site; USD 65,000 - 85,000; Full time

Benefits offered by this job

Health Insurance

Tuition Reimbursement

Vacation/Holiday/Sick Time

Flexible Spending & Health Savings

Work/Life Balance

401(k) with Company match

Pet Insurance

Job summary

Parexel is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

You will conduct onsite monitoring activities, build and maintain productive site relationships, address site issues, and support

Qualifications

• 12+ months of direct onsite monitoring experience as a CRA.
• Bachelor’s degree or equivalent in biological science, pharmacy, or another health-related discipline.
• Knowledge of GCP, regulatory requirements, and clinical trial processes.
• Experience with CTMS/EDMS and MS Office applications.
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, Ophthalmology, CAR-T, and/or MASH trial monitoring experience preferred.

Responsibilities

• Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned sites.
• Manage site quality and delivery from identification through closeout.
• Serve as primary contact for assigned sites, addressing questions and resolving issues.
• Oversee study integrity and build relationships with investigators and site staff.
• Review trial performance and safeguard participant rights, safety, and well-being.
• Develop patient recruitment strategies to support enrollment timelines.
• Ensure compliance with SOPs, protocols, and regulatory requirements.
• Evaluate data quality, site performance, and investigational product accountability.
• Verify completeness and quality of regulatory documentation and site records.

Skills

Site relationship management

Communication skills

Problem-solving

Independent work

Prioritization

Education

Bachelor’s degree in health sciences

Tools

CTMS

EDMS

MS Office (Excel/Word)

Job description

Parexel is seeking a Clinical Research Associate (CRA) with at least 12 months of onsite monitoring experience to join our team. As a CRA, you will manage clinical sites from identification through closeout, serving as the primary point of contact for site teams and helping ensure study quality, patient safety, regulatory compliance, and accurate clinical data.

You will conduct onsite monitoring activities, build and maintain productive site relationships, address site issues, and support