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.
• 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.
• Aid 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.

Requirements

• 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.

Qualifications

• None specified.

Skills

• Strong communication skills.
• Attention to detail.
• Data management proficiency.
• Ability to work independently and as part of a team.
• Knowledge of GCP and regulatory requirements.

Benefits

Best-in-class benefits and perks include:

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

Pay

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.

Schedule

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

Location

START New Jersey - 629 Cranbury Rd., Suite 102, East Brunswick, New Jersey 08816