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Jobs · Analyst · New York

Oncology Clinical Research Coordinator

The START Center for Cancer Research · Lake Success, NY · 1 wk ago
On-siteAnalyst$45–$60/hrFull-time

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. Throughout our history, START has provided hope to cancer patients in global community practices by offering "Hope Through Access" to cutting edge trials throughout the United States and Europe. We are hiring a Clinical Research Coordinator to work under the guidance of senior research staff 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.
  • Maintain files using standardized study document labeling and filing procedures.
  • Create/review forms created or revised for assigned trials to assure protocol compliance.
  • Implement initial protocol and amendments, training staff who will be involved in patient treatment and management.
  • Maintain an up-to-date contact list.
  • Aid in 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.
  • Aid the 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.
  • Time management.
  • Communication.
  • Protocol adherence.
  • Microsoft Office Suite.
  • Clinical trial management software.

Benefits

We value the time, talent, and dedication our employees bring to START. Our commitment to your well-being and growth is reflected in a competitive compensation package—based on experience—along with comprehensive benefits designed to support you both personally and professionally:

  • 401(k) retirement savings plan with employer match.
  • 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.

Pay

$45.00 to $60.00 per hour, based on experience, qualifications, and internal equity.

Schedule

8:00 am-5:00 pm EST, Monday-Friday

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