Senior Clinical Research Coordinator - Oncology

Vitalief•Newark, NJ

3d•$75,000 - $85,000•Hybrid

About The Position

Vitalief is seeking an experienced Senior Clinical Research Coordinator (CRC) to join our team as a full-time employee with a comprehensive benefits package. This role will support a portfolio of Phase II–IV oncology interventional clinical trials at a community hospital site in Newark, NJ. The ideal candidate will have a minimum of three years of clinical research coordination experience, a strong background supporting oncology trials across multiple disease areas, experience mentoring junior CRC team members, and the ability to excel in a collaborative, small-team environment.

Requirements

Bachelor’s degree in health science, life science, nursing, or a related field.
Minimum of 3 years of clinical research coordination experience supporting interventional Phase II–IV clinical trials.
Required oncology clinical trial experience, preferably with exposure to multiple oncology disease areas.
Experience with patient identification, pre-screening, informed consent, enrollment, retention, regulatory compliance, and clinical data management.
Prior experience mentoring or supporting the development of junior CRCs.
Proficiency with EPIC and OnCore™ CTMS.
Ability to manage multiple concurrent studies while maintaining strong attention to detail and organization.
Adaptable, solutions-oriented mindset with the ability to work effectively in a small, collaborative team environment.
Strong interpersonal and communication skills with the ability to work closely with physicians, nurses, research staff, hospital departments, and external partners.
Experience ensuring SAEs are documented, completed, and reported within protocol-defined timelines.
Proficiency with Microsoft Office applications and clinical research systems.

Responsibilities

Support the execution of Phase II–IV oncology clinical trials, including pharmaceutical-sponsored, ECOG, and investigator-initiated studies.
Manage trials across multiple oncology disease groups, including GYN, Breast, GI/GU, Head & Neck, and Lung cancers.
Oversee a portfolio of approximately 15–20 active clinical trials in a fast-paced, high-volume clinical environment.
Identify and screen potential study participants using physician schedules, pathology reports, multidisciplinary tumor boards, referrals, and other clinical resources.
Obtain informed consent and enroll eligible patients in accordance with protocol requirements and regulatory standards.
Manage patients throughout the clinical trial lifecycle, from consent through completion of active treatment.
Educate patients regarding study procedures, treatment schedules, and protocol requirements.
Coordinate patient care activities with physicians, infusion teams, nursing staff, radiology, pathology, laboratories, and other clinical departments.
Monitor patient safety, document clinical outcomes, and ensure timely reporting of adverse events and Serious Adverse Events (SAEs).
Maintain accurate clinical trial documentation, source records, regulatory files, patient calendars, and study-related documentation.
Ensure compliance with study protocols, Good Clinical Practice (GCP), institutional policies, and regulatory requirements.
Provide guidance and mentorship to junior CRC team members and support team collaboration.