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For Companies At a Glance
- Tasks: Support cancer care by coordinating clinical trials and assessing patient eligibility.
- Company: Join Virginia Oncology Associates, the leading cancer care group in Hampton Roads and Northeast North Carolina.
- Benefits: Enjoy a collaborative work environment with opportunities for professional growth and development.
- Why this job: Make a real impact in patients' lives while working in a dynamic and supportive team.
- Qualifications: Requires an associate's degree; nursing experience preferred for RN candidates.
- Other info: Work involves exposure to oncology environments; reasonable accommodations available.
The predicted salary is between 36000 - 60000 £ per year.
Overview
Virginia Oncology Associates, the largest group of medical professionals in Hampton Roads and Northeast North Carolina devoted exclusively to cancer care and blood disorders, has an exciting opportunity for a Clinical Research Coordinator or Clinical Research RN to support our office in Norfolk.
***Please take this quick survey once you\’ve submitted your resume to complete the application process: Clinical Research PI Link
****If you have completed the survey before, even for another position, please do not take it again.
Responsibilities
- Present trial concepts, objectives and treatment details to potential patients for various clinical therapy trials, while conducting detailed assessment and screening to determine their eligibility.
- Participating in the informed consent process and enrolling patients on protocol
- 80% of the job will be computer based, and direct patient care is limited in a non-RN Clinical Research Coordinator role
- Collects and maintains regulatory documents in accordance with USOR SOP and applicable regulations. Participates in scheduling monitoring and auditing visits, as well as interacting with the monitors/auditors while onsite.
- Coordinating patient care in compliance with protocol requirements
- Collaborating with the physician to review patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to drug study and thoroughly documenting all findings
- Working directly with other research bases and/or sponsors
- Overseeing the preparation of orders by physicians to assure that protocol compliance is maintained
- Communicating with physicians regarding study requirements, need for dose modification and adverse event reporting
Qualifications
- Associates degree in a clinical or scientific related discipline required
- Experience in clinical research preferred
- Experience with computer data entry and database management
- Excellent written and oral communication skills
- Ability to read, analyze, and interpret technical procedures such as protocols, informed consent, and regulatory documents
Additional Qualifications for Nurse Candidates:
- Graduate from an accredited program for nursing education (BSN preferred) preferred
- Minimum of one (1) year nursing experience preferably in oncology
- Current licensure as an RN in Virginia preferred
- Current BCLS or ACLS certification required
- OCN, SoCRA, or ACRP certification preferred
WORK ENVIRONMENT:
The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Exposure to communicable diseases, toxic substances, ionizing radiation, medical preparations and other conditions common to an oncology/hematology clinic environment. While performing the duties of this job, the employee is regularly exposed to direct contact with patients with potential for exposure to toxic substances, medicinal preparations, and chemotherapeutic agents.
PHYSICAL DEMANDS:
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. Requires full range of body motion including handling and lifting patients, manual and finger dexterity, and eye-hand coordination. Requires standing and walking for extensive periods of time. Occasionally lifts and carries items weighing up to 40 lbs. Requires corrected vision and hearing to normal range.
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Clinical Research Coordinator, Nurse (RN) employer: DaVita Inc.
Contact Detail:
DaVita Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator, Nurse (RN)
✨Tip Number 1
Familiarise yourself with the latest clinical research protocols and oncology treatments. This knowledge will not only help you during interviews but also demonstrate your genuine interest in the field.
✨Tip Number 2
Network with professionals in the oncology and clinical research fields. Attend relevant conferences or local meetups to connect with potential colleagues and learn about job openings before they are advertised.
✨Tip Number 3
Prepare for the interview by practising how to present trial concepts and patient eligibility criteria clearly. Role-playing with a friend can help you articulate your thoughts and feel more confident.
✨Tip Number 4
Stay updated on regulatory requirements and compliance standards in clinical research. Being knowledgeable about these aspects will set you apart as a candidate who understands the importance of protocol adherence.
We think you need these skills to ace Clinical Research Coordinator, Nurse (RN)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research and nursing. Emphasise any oncology-related roles or certifications, as well as your ability to manage data entry and regulatory documents.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the responsibilities mentioned in the job description. Discuss your experience with patient care, informed consent processes, and your familiarity with clinical trial protocols.
Highlight Communication Skills: Since excellent written and oral communication skills are crucial for this role, provide examples in your application of how you've effectively communicated with patients and medical professionals in past positions.
Complete the Survey: After submitting your resume, don't forget to complete the quick survey linked in the job description. This step is essential to finalise your application process.
How to prepare for a job interview at DaVita Inc.
✨Know Your Clinical Research Basics
Make sure you brush up on the fundamentals of clinical research. Understand trial phases, informed consent processes, and regulatory requirements. This knowledge will help you answer questions confidently and demonstrate your expertise.
✨Highlight Relevant Experience
Be prepared to discuss your previous experience in clinical research or nursing, especially in oncology. Share specific examples of how you've contributed to patient care or research protocols, as this will show your suitability for the role.
✨Demonstrate Strong Communication Skills
Since the role involves presenting trial concepts and collaborating with physicians, practice articulating complex information clearly and concisely. You might be asked to explain a protocol or consent process, so being able to communicate effectively is key.
✨Prepare Questions for the Interviewers
Think of insightful questions to ask about the team, the research projects, or the company culture. This shows your genuine interest in the position and helps you assess if it's the right fit for you.
