Qureos Mentor

United Urology Group

<div><h1 class="jobSectionHeader">Advanced Practice Provider Opportunity</h1>
<h3 class="jobSectionHeader">Chesapeake Oncology Hematology Associates</h3>
<h5 class="jobSectionHeader">Glen Burnie, MD</h5> 


Job Summary

Occupation: Nurse Practitioner or Physician Assistant

Specialty: Hematology/Oncology

Clinic Location: Glen Burnie, MD

Employment: Full-Time | Mon-Fri

Setting: Private Practice, Outpatient/Inpatient

Board Certifications: NP-C/PA-C

Ideal Candidate:
<ul>
<li>1-2 years of NP/PA experience required</li>
<li>Hematology/Oncology experience as RN or APP preferred</li></ul> 


About the Role

Chesapeake Oncology Hematology Associates is seeking an Advanced Practice Provider to support its hematology and oncology team. In this role, you will be closely involved in medical oncology care, with a clinical focus on chemotherapy and immunotherapy treatments, working alongside physicians and infusion staff to ensure safe, coordinated care. The position offers a mix of outpatient and inpatient exposure within a collaborative private practice environment that values clinical excellence and patient relationships. This opportunity is ideal for an APP who enjoys hands‑on oncology care and contributing meaningfully across the treatment continuum. 


About Glen Burnie, MD

Glen Burnie, Maryland is a well‑established community in Anne Arundel County, offering convenient access to both Baltimore and Washington, DC. The area is known for its suburban feel, diverse neighborhoods, and strong local amenities, including shopping centers, dining, and parks. Glen Burnie's central location provides easy access to major highways, public transportation, and Baltimore/Washington International Thurgood Marshall Airport, making commuting and travel simple. With a mix of residential comfort, accessibility, and proximity to major employment and healthcare hubs, Glen Burnie is a practical and appealing place to live and work. 


Recruitment Package

Top-Tier Compensation &ndash; Highly competitive compensation structures

Comprehensive Benefits &ndash; Medical, Dental, Vision, Disability, Life

Retirement Plan &ndash; Secure your future, 401k match

Work-Life Balance &ndash; Paid time off

Professional Growth &ndash; CME days and reimbursement

Community Care &ndash; Make a real difference by caring for patients in their local communities 


Salary Transparency

Exact compensation may vary based on skills, experience, and location.

Base Salary Range: between $115,000 - $135,000 annually 


About the Practice

At Chesapeake Oncology Hematology Associates, our practice has been serving across central Maryland for over 25 years with compassionate, comprehensive cancer care close to home. With multiple locations including Glen Burnie, Columbia, Annapolis, and Stevensville, we are proud to offer patients access to cutting-edge treatment close to home. Our team of dedicated staff specializes in a variety of cancers and blood disorders, including breast, lung, colorectal, gynecologic, and hematologic malignancies. We offer a full spectrum of services such as chemotherapy, immunotherapy, radiation, iron infusions, and in-house lab and pharmacy support. Our mission is to deliver personalized, evidence-based care while supporting our patients and their families every step of the way.

United Urology Group is a national network of leading urology practices dedicated to delivering high-quality, patient-centered care in local communities. In partnership with OneOncology, UUG is part of an integrated ecosystem of Urology, Medical Oncology, and Radiation Oncology, providing patients with seamless, coordinated care across all aspects of their treatment. Our physician-led, data-driven, and technology-enabled platform empowers care teams with shared resources, clinical collaboration, and access to cutting-edge research and multi-center clinical trials through OneR. By combining local relationships with national expertise, UUG ensures patients receive exceptional, compassionate care without leaving their communities. 


If you would like to apply or learn more about this opportunity, please email your CV to rachel.rogers@oneoncology.com 


I look forward to speaking with you!</div>

Advanced Practice Provider - Chesapeake Oncology Hematology Associates

<div>
 Why Join Us?
 
 
 At United Urology Group, our employees are at the heart of our mission and have incredible opportunities to impact our patients' lives with their urologic care.
 
 
 We foster a culture that thrives on compassion, teamwork, integrity, and diversity, all of which start with our staff! We deliver a cohesive approach to urologic care that provides patients with access to experienced specialists, a superb team of healthcare professionals, and the most advanced technology for patient treatments and therapies. We offer competitive salaries and a great work/life balance: enjoy your weekends! UUG offers outstanding benefits, including tuition reimbursement, health, dental, and vision insurance, corporate discounts, and much more!
 
 
 
 Job Description
 
 
 
 The
 
 Research Coordinator
 
 will screen, enroll, and follow study subjects for Phase I, II, III, and IV clinical trials, ensuring protocol compliance and close monitoring while the subjects are on study.
 
 
 
 Primary Duties &amp; Responsibilities
 
 
 
 Conducting Clinical Trials
 
 
 <ul>
 <li>
 Review with the Principal Investigator (PI) the inclusion/exclusion criteria, overall structure, and requirements of each protocol and ensure logistics for site implementation.
 </li>
 <li>
 Review the protocol and the informed consent form for accuracy and clarity.
 </li>
 <li>
 Develop and implement strategies for subject recruitment and ongoing communications with all physicians, research staff, and office staff.
 </li>
 <li>
 Complete new trial feasibilities upon review with potential Investigator and submit to Sponsor/CRO. Complete and submit CDA to Sponsor/CRO in accordance with site Standard Operating Procedures (SOP).
 </li>
 <li>
 Schedule site Sponsor visits in accordance with internal SOP.
 </li>
 <li>
 Prepare study charts, binders, and supplies for offsite storage in conjunction with the Regulatory Specialist, when applicable.
 </li>
 <li>
 Ensure maintenance and calibration of site study required equipment.
 
 
 </li>
 </ul>
 Enrollment of Study Subjects
 
 
 <ul>
 <li>
 Review the study design and inclusion/exclusion criteria with the PI/SI, and if needed the Sponsor to ensure understanding.
 </li>
 <li>
 Review, verify, and record/collect all relevant documentation in the subject&rsquo;s medical record needed to confirm study eligibility.
 </li>
 <li>
 Review the protocol, informed consent form, and follow-up procedures with the potential study subjects.
 </li>
 <li>
 Ensure the current approved informed consent is signed before subjects are screened and enrolled.
 </li>
 <li>
 Inform and document notification of the subject&rsquo;s Primary Care Physician of trial participation if approved by the subject.
 </li>
 <li>
 Perform delegated Protocol specific tasks as assigned by Principal Investigator.
 </li>
 <li>
 Ensure that the randomization procedures are followed and documented per protocol guidelines.
 </li>
 <li>
 Document protocol exemptions and deviations, as appropriate. Ensure duplication of each for filing in the subject source and with the regulatory specialist.
 </li>
 <li>
 Ensure all procedures and documentation of subject participation are kept in accordance with FDA regulations, ICH guidance, and internal SOP.
 
 
 </li>
 </ul>
 Follow-Up Procedures
 
 
 <ul>
 <li>
 Schedule subjects for follow-up visits, collect subjects&rsquo; responses to therapy, and interview subjects for adverse events and changes to concomitant medications. Ensuring that a review of EMR is made during the subject visit for any notable medical/medication changes from the last research visit.
 </li>
 <li>
 Review laboratory data and communicate abnormal values to the PI/SI and as needed, primary care provider or specialist if additional medical attention is needed.
 </li>
 <li>
 Assess and document subject compliance and accountability with Investigational Product (IP). Document re-education when appropriate.
 </li>
 <li>
 Communicate with research staff to ensure timely and accurate study drug distribution when applicable.
 </li>
 <li>
 Administer study drug therapy as needed and maintain the study drug dispensing log if a pharmacist is not involved.
 </li>
 <li>
 Record all Adverse Events outlined in protocol and review them with the PI/SI.
 </li>
 <li>
 Report all Serious Adverse Events to the principal investigator, sponsor, and IRB as outlined in the protocol and site SOP. If need be, contact the subject&rsquo;s primary care physician or specialist.
 
 
 </li>
 </ul>
 Administrative/Clerical
 
 
 <ul>
 <li>
 Reporting all Deviations/Adverse/SAE within Sponsor/IRB&rsquo;s timeframe and in accordance with site SOP.
 </li>
 <li>
 Follow SOPs/GCPs/HIPPA according to the site, sponsor, ICH, and FDA.
 </li>
 <li>
 Maintenance of accurate and complete documentation, including but not limited to signed informed consent forms, source documentation, drug dispensing logs, subject logs, and study-related communications.
 </li>
 <li>
 Follow up and document outstanding action items on Monitoring reports, ensure PI/SI oversight, and that the site Regulatory Specialist receives reviewed/corrected/signed copy of the report.
 </li>
 <li>
 File appropriate regulatory or Sponsor communications with the site Regulatory Specialist.
 </li>
 <li>
 Create and maintain Master Subject Log and Visit Log.
 
 
 </li>
 </ul>
 Please note this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities required of the employee for this job. Duties, responsibilities, and activities may change at any time, with or without notice.
 
 
 
 Qualifications
 
 
 
 <ul>
 <li>
 Minimum High School Diploma or GED required.
 </li>
 <li>
 Minimum of two (2) years of clinical research experience.
 </li>
 <li>
 Maintained certification of accreditation (CCRC/IATA/CPR/NIH/CITI) required and will be verified prior to employment.
 
 
 </li>
 </ul>
 
 Knowledge, Competencies &amp; Skills
 
 
 
 <ul>
 <li>
 Exceptional customer service skills.
 </li>
 <li>
 Strong attention to detail, a willingness to learn &amp; the ability to stay organized.
 </li>
 <li>
 Ability to perform clinical assessments.
 </li>
 <li>
 Strong understanding of FDA clinical trial phases I-IV.
 </li>
 <li>
 Strong understanding of GCP set forth by the ICH.
 </li>
 <li>
 Proficient knowledge of medical terminology.
 </li>
 <li>
 Proficient knowledge of Research-related Terminology.
 </li>
 <li>
 Strong communication skills, both verbal &amp; written.
 </li>
 <li>
 Proficient computer software and database skills.
 </li>
 <li>
 Comfortable working in a fast-paced environment.
 </li>
 <li>
 Very comfortable asking probing questions to patients, if applicable.
 </li>
 <li>
 Must demonstrate a caring, compassionate, and patient attitude.
 </li>
 <li>
 Maintain HIPAA compliance.
 </li>
 <li>
 Multitasking and proactive problem-solving.
 </li>
 <li>
 Ability to type a minimum of 40 words per minute.
 
 
 </li>
 </ul>
 
 Job Type:
 
 Full-Time
 
 
 
 Pay Range:
 
 $30.00 - $31.50 per hour
 
 
 Actual compensation offered to candidates is based on work experience, education, skill level, and geographic location. Compensation may vary depending on the state or region in which the position is located, in accordance with applicable laws.
 
 
 This position has no close date. Applications will be accepted until an offer has been extended and accepted.
 
 
 
 Equal Opportunity Employer:
 
 Our Practice is an equal opportunity employer. We do not discriminate on the basis of race, color, religion, age, sex, national origin, disability, veteran status, or sexual orientation.
 
 
 The successful candidate(s) for any UUG position will be subject to a pre-employment background check.
</div>

Research Coordinator

Join United Urology Group and explore 2   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

United Urology Group

About Company

Advanced Practice Provider - Chesapeake Oncology Hematology Associates

Research Coordinator