Oncology Clinical Research Coordinator – Early-Phase Trials

START Center for Cancer Research; Myrtle Beach (SC); On-site; USD 50,000 - 70,000; Full time

Benefits offered by this job

401(k) retirement savings plan with{

Job summary

The START Center for Cancer Research is seeking a Clinical Research Coordinator to support daily activities of early phase oncology trials. You will work under senior staff to ensure protocol adherence, informed consent, data accuracy, and patient safety across multiple protocols.

Responsibilities include site coordination, screening, document handling, and regulatory compliance. The role emphasizes communication with sponsors, CROs, and study teams, with a standard M-F schedule at our Myrtle

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.

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.
• Other duties may be assigned at any time.

Skills

Attention to detail

Strong communication

Organizational skills

Time-management

Professional interaction with patients

GCP knowledge

Microsoft Office Suite

Clinical trial management software

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research is seeking a Clinical Research Coordinator to support daily activities of early phase oncology trials. You will work under senior staff to ensure protocol adherence, informed consent, data accuracy, and patient safety across multiple protocols.

Responsibilities include site coordination, screening, document handling, and regulatory compliance. The role emphasizes communication with sponsors, CROs, and study teams, with a standard M-F schedule at our Myrtle