Clinical Research Coordinator

About the role

The START Center for Cancer Research (“START”) is the world’s largest early phase site network, fully dedicated to oncology clinical research. We are currently hiring a Clinical Research Coordinator to support the daily activities of early phase oncology clinical trials.

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.
• Affiliate 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.
• Afford assistance with 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.

Requirements

• 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.

Qualifications

• Experience working in an oncology setting.

Skills

• Attention to detail.
• Data accuracy.
• Time management.
• Communication.
• Professionalism.
• Interpersonal skills.
• Knowledge of GCP and regulatory requirements.
• Microsoft Office Suite proficiency.

Benefits

We offer a competitive compensation package, including a 401(k) retirement savings plan with employer match, an annual performance bonus, generous paid time off and holidays, comprehensive medical, dental, and vision coverage, and flexible FSA and HSA plans. We also provide employee assistance programs, life and disability insurance, and a supportive environment that values balance, wellbeing, and flexibility.