Clinical Research Monitoring (CRA)

The Clinical Research Assistant supports the conduct of clinical trials by performing protocol-required procedures, coordinating study activities, and engaging directly with study participants. This role is responsible for collecting and documenting clinical data, obtaining informed consent, managing investigational product accountability, processing biological samples, and maintaining regulatory documentation. The Clinical Research Assistant ensures compliance with study protocols, regulatory requirements, and company policies while meeting timelines and delivering high-quality support to patients, investigators, and internal teams.

Collect patient medical histories and obtain informed consent.

• Perform protocol-specific procedures, including EKGs, vital signs, and phlebotomy.
• Collect, process, and ship biological samples (e.g., Verify accuracy of collected clinical data and ensure timely documentation.
• Support temperature monitoring and investigational product (IP) storage.
• Interact directly with COVID-19-positive patients when required.
• Manage study startup documentation, training, and adherence to timelines.
• Adhere to all company policies, procedures, and compliance standards.
• Maintain strict patient confidentiality and regulatory compliance.
• Bachelor's degree in Biology or a related field, or equivalent clinical experience, is preferred.
• Proficiency in Microsoft Office and electronic data systems is required.
• Strong knowledge of medical terminology.
• Ability to work independently with minimal supervision.
• Outstanding customer service skills with both internal teams and external stakeholders.

Candidates who will require immigration or visa sponsorship at any time now or in the future (including, but not limited to, H-1B, TN, or STEM OPT training plans) are not eligible for this role.

Benefits: Medical, Dental, Vision, 401k, PTO and more!

Location: Monday - Friday / on-site / Rochester, NY

At Alliance Clinical Network, our mission is to advance medical research by enrolling diverse populations in high-quality clinical trials. We are committed to maintaining the highest standards of integrity and excellence, and to ensuring that every participant receives respectful and compassionate care. We strive to build a tightly knit, supportive and collaborative environment where our team members can thrive and make meaningful contributions to human health.