Job Description
Summary
This position provides with day to day activities of clinical trials. Many of these duties will include monitoring of research participants, enrollment, and screening. Responsibilities require flexibility and detail oriented individual to work closely with senior research staff. Performs patient screening, blood draws, plans and schedules study visits, does reporting for IRBS, FDA, and Data Safety Review Committee.
Job Duties
- Coordinates day-to-day activities of research protocols, including screening, enrollment, and monitoring of research participants.
- Ensures accurate data collection, documentation, organization, and the safety of research participants.
- May supervise other research staff.
- Coordinates assignments involving research specialties, clinic staff, and hospital staff to ensure protocol adherence and that studies are conducted in accordance with Good Clinical Practice (GCP) guidelines.
- Maintains daily coordination activities while working to minimize clinic visits and complete study procedures in a manner that does not interfere with routine clinical care.
- Conducts comprehensive assessments of adverse events in collaboration with the participant's physician and other care team members. Assesses, documents, and grades adverse events in accordance with standardized NCI guidelines.
- Reports adverse events to the sponsor, as appropriate. Understands which adverse events may require modifications, such as dose delays, dose modifications, or supportive care, and effectively communicates this information to the treating physician and/or care team.
- Serves as the primary point of contact for clinical trial participants. In collaboration with departmental physicians, assesses whether symptoms may be related to the investigational product, the disease under study, other medications, or a combination of these factors. Obtains appropriate information from participants, determines when escalation is necessary, and evaluates the potential impact on study conduct.
- Performs other job duties as assigned.
Minimum Qualifications
- Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
- Two years of relevant experience.
Preferred Qualifications
- Oncology research study experience.
- Spanish speaking.
Work Authorization Requirement:
This position is not eligible for visa sponsorship. Candidates must be legally authorized to work in the United States at the time of application and throughout the duration of employment.
Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.
Baylor College of Medicine fosters diversity among its students, trainees, faculty and staff as a prerequisite to accomplishing our institutional mission, and setting standards for excellence in training healthcare providers and biomedical scientists, promoting scientific innovation, and providing patient-centered care. - Diversity, respect, and inclusiveness create an environment that is conducive to academic excellence, and strengthens our institution by increasing talent, encouraging creativity, and ensuring a broader perspective. - Diversity helps position Baylor to reduce disparities in health and healthcare access and to better address the needs of the community we serve. - Baylor is committed to recruiting and retaining outstanding students, trainees, faculty and staff from diverse backgrounds by providing a welcoming, supportive learning environment for all members of the Baylor community.
Apply Now
Please mention to the employer that you saw this ad on DiversityWork.com
- Share this job:
- [Save this Job]