Clinical Research Assistant

Alliance Clinical Network; Houston (TX); On-site; USD 52,000 - 68,000; Full time

Job summary

Alliance Clinical Network is seeking a Clinical Research Assistant to support clinical trials in our Houston Operations. You will collect data, obtain informed consent, and manage sample handling while ensuring high-quality documentation and regulatory compliance.

The role requires independent work, strong communication, and careful adherence to study protocols. A biology background and proficiency with MS Office are preferred for effective collaboration with investigators and teams.

Qualifications

• 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.
• Excellent verbal, written, and interpersonal communication skills.
• Strong problem-solving skills and the ability to adapt quickly in a dynamic environment.
• Outstanding customer service skills with both internal teams and external stakeholders.

Responsibilities

• Communicate effectively and courteously with study participants.
• Collect patient medical histories and obtain informed consent.
• Dispense and manage study drug accountability per protocol.
• Perform protocol-specific procedures, including EKGs, vital signs, and phlebotomy.
• Collect, process, and ship biological samples (e.g., blood, urine, tissue).
• 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.
• Ensure all protocol requirements and deadlines are met consistently.
• Adhere to all company policies, procedures, and compliance standards.
• Maintain strict patient confidentiality and regulatory compliance.

Skills

Verbal communication

Written communication

Interpersonal communication

Problem solving

Adaptability

Customer service

Education

Bachelor’s degree in Biology or related field

Tools

Microsoft Office

Electronic data systems

Job description

If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

Clinical Research Assistant

Clinical Operations - Site FullTime Technical Houston, Houston, TX, US

2 days ago Requisition ID: 1372

Summary:

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.

Essential Duties and Responsibilities:

• Communicate effectively and courteously with study participants.
• Collect patient medical histories and obtain informed consent.
• Dispense and manage study drug accountability per protocol.
• Perform protocol-specific procedures, including EKGs, vital signs, and phlebotomy.
• Collect, process, and ship biological samples (e.g., blood, urine, tissue).
• 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.
• Ensure all protocol requirements and deadlines are met consistently.
• Adhere to all company policies, procedures, and compliance standards.
• Maintain strict patient confidentiality and regulatory compliance.
• Perform other duties as assigned.

Qualifications:

• 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.
• Excellent verbal, written, and interpersonal communication skills.
• Strong problem-solving skills and the ability to adapt quickly in a dynamic environment.
• Outstanding customer service skills with both internal teams and external stakeholders.

ACN does not provide visa sponsorship for this role. 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.

About the Company:

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