Clinical Research Coordinator

The START Center for Cancer Research; East Brunswick Township (NJ); On-site; USD 52,000 - 62,000; Full time

Benefits offered by this job

401(k) match

Performance bonus

Paid time off

Medical, dental, vision coverage

Life and disability insurance

Employee Assistance Program (EAP)

Flexible FSA/HSA plans

Collaborative culture

Job summary

The START Center for Cancer Research in East Brunswick, NJ is seeking a Clinical Research Coordinator to support the daily activities of early‑phase oncology clinical trials under supervision of senior staff. The CRC ensures accurate conduct of trials, adherence to protocols and patient safety standards.

The role involves direct patient interaction, data collection, regulatory compliance, and coordination of multiple protocols.

Qualifications

• High School Diploma or GED.
• 2 years of clinical research experience supporting interventional studies.
• Strong experience 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.
• Working knowledge of GCP and regulatory requirements.
• Proficient in Microsoft Office Suite and clinical trial management software.

Responsibilities

• Communicate with Study Sponsors, CROs, staff regarding questions and protocol status.
• Monitor day-to-day conduct of studies per protocol, SOPs, and GCP.
• Create/review forms for trials to assure protocol compliance.
• Maintain study files with standardized labeling and filing.
• Assist with patient screening and eligibility determination.
• Facilitate informed consent process ensuring proper completion.
• Address deviations with leadership to prevent recurrence.
• Assist data coordinator with CRF completion and query resolution.
• Work with PI to complete and submit Serious Adverse Event reports.
• Perform protocol closeout activities with data coordinator.

Skills

Clinical research

Oncology trials

GCP knowledge

Data management

Attention to detail

Education

High School Diploma or GED

Tools

Microsoft Office Suite

Clinical trial management software

Job description

The START Center for Cancer Research ("START") is the world’s largestearly phasesite network, fully dedicated tooncologyclinical research.Throughout ourhistory, START has provided hope to cancer patients inglobalcommunity practices by offering "Hope Through Access” tocutting edgetrials throughout the UnitedStatesand 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 range for this role is $38 - $45/hour. However, base pay may vary depending on multiple individualized factors including market location, job-related knowledge, skills, and experience.

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

Location: 629 Cranbury Rd., Suite 102, East Brunswick, New Jersey 08816

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.

- 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.

Required Education and Experience:

- High School Diploma or GED.

- 2 years of clinical research experience supporting interventional studies

- Strong experience 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.

- Working knowledge of GCP and regulatory requirements.

- Proficient in Microsoft Office Suite and clinical trial management software.

Best-in-Class Benefits and Perks

We value the time, talent, and dedication our employees bring to START. Our commitment to yourwell-beingand 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 coverageand optional insuranceoptions

- Companyp‑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’recommitted to fostering a collaborative, creative workplace where every team member is encouraged to contribute. At START,you’lljoin 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. STARTrepresentsthe 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 .

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.