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
• 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

Preferred

• Experience working in an oncology setting

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
• Employee Assistance Program (EAP) providing confidential, no-cost support for you and your family from day one
• Flexible FSA and HSA plans
• A supportive environment that values balance, wellbeing, and flexibility
• A collaborative, creative workplace where every team member is encouraged to contribute
• A team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation
• 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
• 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
• Experience working in an oncology setting
• 2 years of clinical research experience.

Required skills

• Clinical Research, Clinical Research Regulatory Requirements, Oncology Clinical Trials (Phase 1)

Preferred skills

• Experience working in an oncology setting

Experience

• 2+ years