Clinical Research Associate – Onsite Monitoring Pro

Parexel; Richmond (VA); Sur place; USD 64 000 - 98 000; Plein temps

Avantages offerts par ce poste

Health insurance

Tuition reimbursement

Vacation time

FSAs/HSAs

Work/Life balance

401(k) with company match

Pet insurance

Résumé du poste

Parexel seeks a Clinical Research Associate (CRA) with at least 1 year of onsite monitoring experience to manage clinical sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data.

You will conduct onsite monitoring activities, build productive site relationships, support enrollment, and ensure data integrity using Parexel technology. This role offers growth in clinical research and a collaborative, patient-focused environment.

Qualifications

• 12+ months direct onsite CRA monitoring experience.
• Bachelor's degree or equivalent in biological sciences, pharmacy, or health-related discipline.
• Knowledge of GCP, regulatory requirements, and clinical trial processes.
• Experience using CTMS, EDMS, and Microsoft Office (Excel/Word).
• Strong interpersonal, written, verbal, organizational, and problem-solving skills.
• Oncology, ophthalmology, CAR-T, and/or MASH trial monitoring experience preferred.

Responsabilités

• Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV), and termination visits (TV) at assigned sites, and prepare timely visit and contact reports.

Connaissances

Site relationships

Problem solving

Communication

Independence

Client focus

Adaptability

Multitasking

Quality awareness

Team collaboration

Formation

Bachelor's degree

Outils

CTMS

EDMS

MS Office

Description du poste

Parexel seeks a Clinical Research Associate (CRA) with at least 1 year of onsite monitoring experience to manage clinical sites from identification through closeout, ensuring study quality, patient safety, regulatory compliance, and accurate data.

You will conduct onsite monitoring activities, build productive site relationships, support enrollment, and ensure data integrity using Parexel technology. This role offers growth in clinical research and a collaborative, patient-focused environment.