Remote
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Remote
Job description
Job Summary
The Senior Clinical Research Associate (Sr. CRA) is a vital member of our team, contributing to the successful execution of clinical studies involving both investigational and approved medical products. As part of a WBENC-certified Contract Research Organization (CRO) with a trusted history in clinical research since 1996, this role will support our dedication to high-quality research outcomes and patient safety.
Responsibilities
- Oversee and manage various clinical study sites to ensure compliance with study protocols and regulatory requirements.
- Coordinate monitoring visits to assess data validity and ensure adherence to Good Clinical Practice (GCP).
- Collaborate with cross-functional teams to facilitate effective communication and project timelines.
- Prepare and present reports on study progress, findings, and discrepancies to both internal teams and external stakeholders.
- Support training initiatives for site staff and ensure they are well-informed of study procedures.
Qualifications
- Registered Nurse (RN) or a Bachelor’s degree in a relevant field is required.
- Proven experience in clinical research or monitoring, demonstrating an understanding of clinical trial processes.
- Excellent organizational and communication skills to work effectively in a remote environment.
- Strong analytical abilities to assess data quality and address issues promptly.
- Ability to work independently and manage multiple priorities in a fast-paced setting.
ProTrials Research, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.
