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. The CRC ensures the accurate and timely conduct of clinical research, adhering to protocols, regulatory requirements, and patient safety standards.

This position is offered at a pay range of $30.00 to $44.00 per hour, based on experience, qualifications, and internal equity. In addition, employees in this role may be eligible for an annual bonus of up to 10% of base earnings.

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

Location: 405 Lakeville Road, Entrance A, Lake Success, NY 11042

Essential 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.

Education & Experience

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.

Preferred Education and Experience:

Experience working in an oncology setting.

Physical and Travel Requirements:

Approximately 80% of time is spent sitting.
Very fast-paced and ever-changing healthcare environment.
Demanding deadlines and time frames.
Constant demand for updating knowledge.
Works closely with physicians and ancillary personnel in caring for and treating oncology/hematology patients.

Best-in-Class Benefits and Perks

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: 

Plus, we work to maintain the best environment for our employees, where people can learn and grow with the company. We strive to provide a collaborative, creative environment where everyone feels encouraged to contribute to our processes, decisions, planning, and culture.

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 
Commitment to a supportive environment that values balance, wellbeing, and flexibility 
We’re committed to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START, you’ll join a team that values continuous learning, professional growth, shared ideas, and a culture built on inclusivity and innovation.

More about The START Center for Cancer Research
START clinical trial sites have conducted more than 1,000 early-phase clinical trials, including dozens of therapies that were approved by the FDA or EMA. START represents the world’s largest roster of early-phase principal investigators across its Network of clinical trial sites. Committed to accelerating passage from trials to treatments, START delivers hope to patients, families, and physicians around the world via our mission of “Hope Through Access”. As an example, in San Antonio, where START was founded, START treated the first patient ever with Keytruda – one of the most effective cancer drugs in medical history. 

Learn more at
STARTresearch.com.  

Ready to be part of a team changing the future of cancer treatment?

Join us in our mission to conquer cancer, one clinical trial at a time. Your expertise and dedication can help us bring hope and healing to patients worldwide. Please submit your application online. 

We are an equal opportunity employer that welcomes and encourages diversity in the workplace. We do not discriminate on the basis of race, color, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, state, or local law.

Pay: $30.00 - $44.00 per hour

Benefits:

401(k)
401(k) matching
Health insurance
Paid time off

Experience:

Oncology Clinical Research: 2 years (Required)

Work Location: In person

The START Center for Cancer Research

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Clinical Research Coordinator