Clinical Research Coordinator II-Rockville Division

The US Oncology Network•Rockville, MD

14h•Onsite

About The Position

Join Our Team at Maryland Oncology Hematology! We’re looking for passionate and talented professionals to join our team in providing exceptional cancer care. If you’re dedicated to making a difference for patients, physicians, and colleagues, we want to hear from you! With 15+ locations across Maryland and DC, we offer a dynamic and supportive environment where you can grow and thrive. Explore opportunities with us and apply today! The general pay scale for this position at MOH is $57,841.71- $88,987.25 per year. The actual hiring rate is dependent on many factors, including but not limited to prior work experience, education, job/position responsibilities, location, work performance, etc. Responsible for recruiting, screening, consenting, and enrolling patients in clinical trials. The Clinical Research Coordinator II (CRC II) also coordinates and oversees participant visits in accordance with protocol requirements. Duties include, but are not limited to, assuring protocol compliance for all enrolled participants, participating in the informed consent process, conducting ongoing assessments, and documenting in collaboration with physicians and other providers. Serves as a resource for education and training of clinical staff and assists in problem‑solving complex issues related to implementation of research processes, process improvements, and standard operating procedures (SOPs). Compiles and reports protocol activity, enrollment data, and financial information. Ensures research quality by adhering to organizational SOPs, principles of Good Clinical Practice (GCP), and applicable federal, state, and local regulations, including OSHA, CDC, and HIPAA. Supports and adheres to the company compliance program, including the Code of Ethics and Business Standards.

Requirements

Associate’s degree in a clinical or scientific discipline required; Bachelor’s degree preferred.
Minimum three years of experience in a clinical or scientific field required.
Experience with Microsoft Office applications.
Excellent communication skills.
Strong organizational abilities.
Ability to multi‑task effectively.
Strong time‑management skills.
High level of interpersonal skills to interact with individuals at various levels.
Strong attention to detail.
Ability to work in a fast‑paced environment.
May be responsible for basic clinical assessments.

Nice To Haves

Bachelor’s degree preferred.
SoCRA or ACRP certification preferred.
Experience working with physicians preferred.
Experience in clinical research preferred.

Responsibilities

Screens potential participants for protocol eligibility.
Presents trial concepts and details to participants, participates in the informed consent process, and enrolls participants into clinical trials.
Coordinates participant care in compliance with protocol requirements.
May disburse investigational product and maintain accountability records.
Oversees preparation of orders by providers to ensure protocol compliance.
Packages and ships laboratory specimens to central vendors as applicable.
Completion of Hazmat and/or IATA training may be required.
In collaboration with providers, reviews participants for changes in condition, adverse events, concomitant medications, protocol compliance, and response to study treatment.
Thoroughly documents all findings and participates in data collection.
Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports.
Maintains regulatory documents in accordance with organizational SOPs and applicable regulations.
May assist with scheduling monitoring and auditing visits, and interact with monitors/auditors as needed.
May collaborate with research leadership in study selection processes.
Participates in required training and education programs.
May contribute to education of clinical staff regarding research procedures.
Works with staff to develop action plans and performance improvement initiatives to enhance quality.
May compile and report protocol activity, enrollment trends, data entry compliance, and research financial information to practice leadership and providers.
May review protocol‑specific billing guides and submit billing information to the appropriate personnel.