Contribute to impactful clinical trials in a collaborative environment. Enhance your expertise in clinical research procedures and documentation. Gain valuable experience in a dynamic healthcare setting.
Clinical Research Assistant
in Healthcare + Life Sciences PermanentJob Detail
Job Description
Clinical Research Assistant Overview
- The Clinical Research Assistant will support clinical trials by performing vital signs, ECGs, and other procedures.
- Collaborate closely with Clinical Research Coordinators to ensure accurate documentation and adherence to protocols.
- Assist in coordinating subject care visits, ensuring a smooth and efficient process.
- Participate in training to enhance clinical research knowledge and skills.
- Maintain compliance with Good Clinical Practices and site SOPs.
- Exhibit professionalism and adherence to company policies and applicable laws.
- Contribute to a collaborative team environment and prioritize confidentiality.
- This role offers an opportunity to develop expertise in clinical research operations.
Clinical Research Assistant Key Responsibilities & Duties
- Perform vital signs, ECGs, and specimen processing with precision and accuracy.
- Collaborate with coordinators to complete study documentation and case report forms.
- Assist in scheduling and coordinating subject visits for clinical trials.
- Ensure compliance with clinical trial protocols and Good Clinical Practices.
- Support the team in maintaining high standards of confidentiality and professionalism.
- Contribute to the development and prioritization of multiple tasks effectively.
- Participate in training sessions to enhance clinical research expertise.
- Work constructively within a team environment to achieve project goals.
Clinical Research Assistant Job Requirements
- Associate of Applied Science (AAS) degree or equivalent educational background.
- Minimum of 1 year of experience in a medical assistant, phlebotomist, or similar role preferred.
- Proficiency in performing ECGs, vital signs, and specimen processing.
- Detail-oriented with strong organizational and multitasking abilities.
- Ability to maintain confidentiality and comply with clinical research standards.
- Excellent teamwork and communication skills within a clinical setting.
- Knowledge of Good Clinical Practices and clinical trial protocols.
- Phlebotomy certification or experience is mandatory for this role.
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