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Clinical Research Coordinator
1 month ago
The University of Texas MD Anderson Cancer Center is seeking a highly motivated and detail-oriented Clinical Research Coordinator to join our team. As a Clinical Research Coordinator, you will play a critical role in the coordination and implementation of clinical trials, ensuring the highest level of quality and compliance.
Key Responsibilities:- Coordinate and implement clinical trials, including screening patients, obtaining informed consent, and collecting data.
- Work closely with the research team, including principal investigators, research nurses, and data managers, to ensure seamless trial execution.
- Develop and maintain accurate and up-to-date records, including study protocols, informed consent forms, and case report forms.
- Communicate effectively with patients, families, and healthcare providers to ensure informed decision-making and optimal care.
- Collaborate with the research team to identify and address any issues or concerns that may impact trial conduct.
- Bachelor's degree in a related field, such as nursing, biology, or chemistry.
- At least three years of experience in clinical research, including experience with clinical trials and research protocols.
- Excellent communication and organizational skills, with the ability to work effectively in a fast-paced environment.
- Strong attention to detail and ability to maintain accurate records.
- Ability to work independently and as part of a team, with a strong commitment to quality and compliance.
- Master's degree in a related field.
- Experience with electronic data capture systems and clinical trial management software.
- Certification in clinical research coordination, such as CCRC or CCRA.
The University of Texas MD Anderson Cancer Center is an equal opportunity employer and welcomes applications from diverse candidates. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
