Clinical Research Coordinator
START Center for Cancer Research·East Brunswick Township, New Jersey
START Center for Cancer Research·East Brunswick Township, New Jersey
The Clinical Research Coordinator supports daily activities of early phase oncology clinical trials, ensuring adherence to protocols and regulatory requirements. Key duties include managing patient participation, collecting data, and coordinating with study sponsors and CROs.
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 currently hiring a Clinical Research Coordinator.
The Clinical Research Coordinator (CRC) will 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 role involves direct patient interaction, data collection, and maintaining compliance with Good Clinical Practice (GCP).
The Clinical Research Coordinator will be assigned multiple protocols at any time for which they will oversee the aspects of assigned protocols with planning and coordinating patient participation in the trial.
The hourly pay for this role is $38 - $42/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.
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. Assist with patient screening and determination of eligibility. Facilitate the informed consent process ensuring that consent is appropriately completed. 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.
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. Working knowledge of GCP and regulatory requirements. Proficient in Microsoft Office Suite and clinical trial management software.
Experience working in an oncology clinical research.
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: 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 p‑aid 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 START 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”.
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.
Candidates must have a High School Diploma or GED and at least 2 years of clinical research experience, specifically with a basic understanding of Phase 1 oncology trials. Proficiency in GCP, regulatory requirements, and Microsoft Office is required.
Market context
Clinical Research Coordinator roles in New Jersey are often tied to hospitals, academic medical centers, and oncology research sites, where demand can be steady for candidates who understand trial operations and compliance. This role is competitive because employers typically want prior clinical research experience, GCP knowledge, regulatory familiarity, and comfort with Phase 1 oncology work; review the AI-summarized requirements and benefits here to save time before applying. A practical next step is to tailor your resume to highlight GCP, regulatory documentation, and Microsoft Office experience, plus any oncology trial exposure.
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