Clinical Research Coordinator

Oncology Clinical Research Coordinator (CRC) As an Oncology Clinical Research Coordinator (CRC), you will be an integral part of clinical studies by recruiting participants and collecting and managing study data to support the successful execution of clinical trials. This position is in East Brunswick, New Jersey and is a contract to hire, full time position. Responsibilities Include:

Provide overall coordination of study-related activities for patients enrolled in cancer research studies. Coordinate with Principal Investigators, Supervisor, study sponsors, and CROs to ensure that clinical research activities are performed in accordance with local and federal regulations and adhere to established policies and procedures. Assist in coordinating tests and visits for patients and collaborate with the study team to maximize efficiency and productivity. Assist in IRB submissions and work with the Supervisor to maintain regulatory documents and administrative files for each protocol. Work with research nurses, treating physicians, and Principal Investigators to confirm that each patient meets eligibility criteria for study protocols and enrollment into clinical trials. Maintain patient and regulatory research records. Confer with clinical team members to ensure appropriateness and timeliness of tests. Collect follow-up data on patients post-treatment as required by the protocol. Submit weekly reports to the Supervisor tracking patient screening, enrollment, and subject status. Enter research data into a centralized database according to protocol requirements. Attend investigator meetings as required or requested by the Principal Investigator. Prepare study materials such as informed consent documents, case report forms, enrollment logs, and drug/device accountability logs. If applicable, prepare blinded and unblinded study drugs. If applicable, act as a primary coordinator for the unblinded team. Required Skills

A Bachelor's degree or equivalent working experience required

. Pharmacy Technician certified with infusion drug preparation training preferred. At least one (1) year of clinical research experience Able to travel between offices within the offices in Northeast Jersey area. Preferred Skills

Oncology CRC Experience is a plus Schedule/Shift Monday-Friday 8am-5pm * We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA). * As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.