Clinical Research Assistant

About the Company

Rovia Clinical Research is focused on advancing new treatment options so local patient communities can benefit from better health outcomes. The organization aims to create a supportive, respectful environment where team members are encouraged to learn, contribute, and build meaningful careers. Its workplace culture is shaped by the values of putting people first, staying humble, acting with integrity, working as one team, and being accountable for results.

Role Overview

The Clinical Research Assistant supports the planning and execution of clinical trials while following the study protocol, ICH/GCP standards, sponsor expectations, and internal procedures. The position works closely with the site team to help with study initiation, participant enrollment, data accuracy, and overall trial performance.

Key Responsibilities

• Organize and carry out participant visits according to the approved study protocol.
• Complete clinical procedures as needed, including vital signs, ECGs, specimen collection and processing, and blood draws.
• Make sure informed consent is collected correctly and documented properly.
• Support and educate study participants so they have a positive experience throughout the trial.
• Watch for participant safety issues, document adverse events, and raise concerns when necessary.
• Prepare accurate source documents and enter data into the EDC system in a timely manner.
• Address data queries and maintain strong data quality and integrity.
• Track investigational product inventory and ensure proper storage and handling.
• Help prepare for monitoring visits, audits, and inspections.
• Work with investigators and site staff to support protocol compliance and smooth visit operations.
• Handle additional tasks as assigned.

Required Skills and Knowledge

• Solid understanding of medical terminology and common clinical procedures.
• Working knowledge of ICH/GCP standards and regulatory expectations.
• Strong organization and careful attention to detail.
• Clear communication and strong rapport-building skills with patients.
• Ability to manage several priorities at once in a busy environment.
• Comfort using Microsoft Office, EDC platforms, and CTMS tools.
• Capability to work independently as well as in a team setting.
• Professional conduct and strict respect for patient privacy.

Education and Experience

• High school diploma is required; a bachelor’s degree in a relevant field is preferred.
• Between 0 and 1 year of experience in clinical research.
• Hands-on experience with patient-facing tasks such as phlebotomy, vital signs, and EKGs is required.
• Phlebotomy or Medical Assistant certification is preferred.