The START Center for Cancer Research · 21 hours ago
Clinical Research Coordinator
San Antonio, TX
Full-time
Onsite
Entry Level
2+ years expThe START Center for Cancer Research is the world’s largest early phase site network dedicated to oncology clinical research. They are hiring a motivated Clinical Research Coordinator to support daily activities of early phase oncology clinical trials, ensuring compliance with protocols and patient safety standards.
BiotechnologyHealth CareLife ScienceMedicalOncologyPharmaceutical
Responsibilities
Communicate on a regular basis with Study Sponsor’s, CRO’s, staff, etc. regarding questions, concerns, as well as status of the protocol
Monitor the overall day-to-day conduct of assigned studies in accordance with the specified protocol requirements, Standard Operating Procedures, and Good Clinical Practice to ensure integrity regarding all aspects of the study
Create/review forms created or revised for assigned trials to assure protocol compliance
Maintain files using standardized study document labeling and filing procedures
Implement initial protocol and amendments, training staff who will be involved in patient treatment and management
Maintain an up-to-date contact list
Assist with patient screening and determination of eligibility
Facilitate the informed consent process ensuring that consent is appropriately completed
Prepare and manage source documents according to standard operating procedures
Recognize deviations to the protocol and will work with leadership and staff to address corrective actions to prevent deviations
Assist data coordinator team with case report form completion and query resolution
Work with the Principal Investigator to complete and submit Serious Adverse Event reports
Perform protocol specific closeout related activities in conjunction with the data coordinator
Provide documentation for all deviations whether related to the protocol or a SOP
Ensure that all team members involved understand and adhere to assigned protocols
Qualification
Required
High School Diploma or GED
2 years of clinical research experience
Basic understanding of oncology clinical trials, particularly Phase 1 studies
Strong attention to detail and accuracy in data collection and documentation
Ability to manage multiple tasks and meet deadlines in a fast-paced environment
Excellent organizational and time-management skills
Strong communication skills, both written and verbal
Ability to interact professionally with patients, study staff, and external stakeholders
Working knowledge of GCP and regulatory requirements
Proficient in Microsoft Office Suite and clinical trial management software
Preferred
Experience working in an oncology setting
Benefits
Comprehensive health coverage: Medical, dental, and vision insurance provided
Robust retirement planning: 401(k) plan available with employer matching
Financial security: Life and disability insurance for added protection
Flexible financial options: Health savings and flexible spending accounts offered
Well-being and work-life balance: Paid time off, flexible schedule, and remote work choices provided
Company
The START Center for Cancer Research
The START Center for Cancer Research is a oncology and biotechnology research company.
501-1000 employees
Funding
Current Stage
Late StageLeadership Team
Chris Takimoto
Global Chief Medical Officer
Recent News
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