Clinical Research Coordinator

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
• Assist with patient screening and determination of eligibility
• Facilitate the informed consent process ensuring that consent is appropriately completed
• 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

Benefits

• 401(k) retirement savings plan with employer match
• Eligibility for an annual performance bonus, based on role and company results
• Generous paid time off and paid holidays
• Comprehensive medical, dental, and vision coverage and optional insurance options
• Company-paid life and disability insurance for added financial protection
• Employee Assistance Program (EAP) providing confidential, no-cost support for you and your family from day one
• Flexible FSA and HSA plans to support your financial wellness
• A supportive environment that values balance, wellbeing, and flexibility
• Continuous learning and professional growth opportunities
• A collaborative, creative, inclusive, and innovative workplace where every team member is encouraged to contribute
• The START Center for Cancer Research is a oncology and biotechnology research company.
• San Antonio, Texas, USA
• https://startresearch.com
• Late Stage
• Total Funding
• unknown
• 2024-04-03
• Acquired
• Leadership Team
• Chris Takimoto
• Global Chief Medical Officer
• Recent News
• PR Newswire
• Allegheny Health Network and The START Center for Cancer Research Announce Strategic Collaboration to Expand Patient Access to Early-Phase Cancer Trials
• 2026-08-25
• Bizjournals.com Feed (2025-11-12 15:43:17)
• AHN teams up with START Center to expand early-phase oncology research in western Pennsylvania
• Baptist Health South Florida and The START Center for Cancer Research Announce Strategic Partnership to Expand Patient Access to Early-Phase Cancer Trials
• 2026-05-28
• Company data provided by

Qualifications

• High School Diploma or GED
• 2 years of clinical research experience supporting interventional studies
• Strong experience 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
• Working knowledge of GCP and regulatory requirements
• Proficient in Microsoft Office Suite and clinical trial management software

Required skills

• Clinical Research, Interventional Clinical Studies, Oncology Clinical Trials, Phase 1 Clinical Trials, Clinical Practice (GCP), Regulatory Compliance, Microsoft Office Suite

Experience

• 2+ years