Clinical Research Coordinator Jobs in USA 2025 – Apply Now

A fulfilling existence necessitates adequate health care. Banner Health recognizes this, which is why we exert significant effort each day to enhance the quality of life for our clients. Do you find it alluring to have an impact on both your own life and the lives of others? If so, you may be in for the most extraordinary opportunity of your life.

The Banner MD Anderson Cancer Center Clinical Trials Office is Banner Research’s oncology service line. Banner Gateway Medical Center and Banner MD Anderson Cancer Center are the locations of the department. In order to provide patients with access to trial therapy alternatives and support physician investigators in a safe and ethical manner, the department conducts Phase I–III treatment clinical trials across all illness groups, while adhering to institutional and FDA regulations.

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About Banner Health:

Banner Health’s Banner Gateway Medical Center, a cutting-edge facility, provides state-of-the-art technology and exceptional growth and development opportunities. Banner Gateway provides you with the most advanced tools available to ensure that your patients receive the highest quality of care. These tools include digital radiography, advanced patient monitoring, digital medical records, and physician order entry.

Banner Gateway Medical Center and Banner MD Anderson Cancer Center operate within the same facility. Banner Gateway Medical Center is situated in Gilbert, Arizona, in close proximity to Phoenix. It boasts a 37-bed emergency department, eight surgical suites, and 176 private accommodations.

Oncology, obstetrics, bariatric surgery, emergency care, and other services that are focused on meeting the changing needs of the dynamic and expanding community we serve are among our primary specializations. Banner MD Anderson Cancer Center information The facility, which is situated in Gilbert, Arizona (the Phoenix Metro area), is a component of the Banner Gateway Campus and provides exceptional inpatient and outpatient cancer care. Additionally, it has implemented cutting-edge oncology programs at the Banner Gateway campus, such as comprehensive head and neck cancer care and stem cell transplantation.

There are over 50 infusion bays, a cryopreservation lab, five linear accelerator vaults, a brachytherapy vault, an advanced diagnostic imaging facility with PET/CT scan, and other services that are available. Our inpatient medical oncology unit also has a program that utilizes the electronic surveillance partnership to assist the bedside nurse in patient care. Distant nurses can engage in two-way audio video communication with patients through this program.

Synopsis of the Position:

The individual in this position is accountable for the organization and/or execution of specific protocols. This profession encompasses the following responsibilities: assisting with patient assessments, compiling and documenting medical histories, and maintaining study files.

Primary Functions:

• Gathers pertinent data from patients participating in clinical studies and provides study information. This encompasses the following: assisting with volunteer recruitment and screening, registering patients, providing timely and useful information on clinical trials and protocols to interested parties, recording pertinent medical history from candidates over the phone and in person, gathering pertinent data from the patient’s prior relevant medical records, and outlining the process.
• Performs protocol-required tasks, including obtaining the patient’s medical history, reviewing the system, conducting phlebotomy, taking an EKG, and assessing the patient’s cognitive state. obtains vital indicators. maintains quality control in accordance with established standards. Assists in the interpretation and evaluation of results by gathering information as requested.
• The research physician is informed of adverse events as soon as they occur and they are categorized. Data on the subject’s recommended medical follow-up should be collected from the subject and any secondary sources that are required.
• Patients and their families are furnished with educational resources. He serves as a dependable point of contact for patients and their families in the clinical research program, providing them with resources and support. provides healthcare information to the patient and their family, including preventative measures, health maintenance, and recommendations for diseases associated with the study.
• Consistent protocol implementation is guaranteed by the timely, accurate, and consistent production of the requisite documentation. Assists in the timely and precise completion of pertinent forms for the Institutional Review Board (IRB), informed consent, sponsor correspondence, and other tasks. Participation in the annual IRB approval and updating procedure is permissible.
• Acts as a liaison for community agencies, programmatic areas, and other departments.
• Ensures that the patient’s diagnosis and course of therapy are communicated to the primary referring physicians.
• The capacity to collaborate effectively with others and exhibit knowledge may enable an individual to assume responsibility for the management and implementation of new clinical trials.
• Disciplinary authority It may be necessary for certain positions to engage in frequent communication with patients, relatives, visitors, physicians, and other clinical departments.

Minimum Requirements:

• Understand clinical research methodologies; this is typically achieved by obtaining a bachelor’s degree in a healthcare field.
• The applicant’s objective must be to obtain the Clinical Research Coordinator Certification (CRCC).
• Typically, two to four years of clinical research experience are required.
• Proficiency in medical and clinical terminology.
• It is imperative to possess exceptional organizational and task-management abilities.
• Capacity to safeguard patient and study data privacy.
• It is imperative to be cognizant of the federal and state laws that govern nursing and medicine, as well as the Institute’s policies and procedures.
• It necessitates exceptional interpersonal, organizational, and communication abilities.

Benefits of Jobs:

• Competitive Salary: Clinical research coordinators in the United States receive competitive salaries, which are frequently accompanied by performance incentives, particularly in specialized or high-demand clinical settings.
• Career Advancement Opportunities: Clinical research coordinators have the potential to progress to more senior roles, including clinical research manager, clinical project manager, or director of research, as they accumulate experience. This provides them with the opportunity for long-term career development.
• Job Security: The pharmaceutical and medical device industries’ expansion in the United States has resulted in a significant demand for experienced coordinators, as clinical research is a burgeoning field.
• Skill Development: This position provides the opportunity to cultivate a diverse array of skills, such as data analysis, research methodologies, regulatory compliance, and patient management, all of which are highly beneficial in the healthcare and research sectors.
• Impact on Medical Advancements: Clinical research coordinators are essential in the advancement of medical science, as they oversee trials that contribute to the development of new medical devices, medicines, or treatments.
• Work in a Collaborative Environment: Coordinators frequently collaborate with regulatory bodies, physicians, and researchers, nurturing a dynamic, team-oriented environment that promotes professional development and knowledge exchange.
• Exposure to Cutting-Edge Research: Clinical research coordinators frequently have access to the most recent medical advancements, which enables them to be at the vanguard of new technologies and treatments.
• Employee Benefits: Various employers provide benefits, including health insurance, paid time off, retirement plans, and professional development allowances, which contribute to the total compensation package.
• Opportunities for Specialization: As a clinical research coordinator, you have the flexibility to specialize in a variety of disciplines, including neurology, cardiology, oncology, or pharmacology, thereby customizing your career to your interests.
• Strong Job Demand: The healthcare sector’s increasing demand for clinical trials guarantees a consistent demand for trained research coordinators, offering job security and opportunities throughout the nation.
• Networking Opportunities: The position offers a plethora of opportunities to establish connections with healthcare professionals, researchers, and industry specialists, which may result in additional career opportunities or collaborations.
• Global Exposure: Clinical research coordinators may have the opportunity to participate in global research initiatives, which can contribute to the enhancement of global health, due to the fact that clinical trials are frequently conducted internationally.
• Potential for Remote Work: Clinical research coordinators may have the opportunity to work remotely in certain circumstances, particularly if they are responsible for managing data, documentation, or coordinating remote trials.
• Job Satisfaction: The work of clinical research coordinators is often considered to be fulfilling due to the fact that they are able to contribute to the development of novel treatments and improve patient care outcomes.
• Professional Recognition: Clinical research coordinators who acquire certifications from organizations such as the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA) are frequently acknowledged as experts in their field, which can result in increased career prospects.

What Are Clinical Research Coordinator Jobs in USA?

Clinical Research Coordinators are professionals who supervise and manage clinical trials and research studies to ensure that they are conducted in a manner that is both efficient and compliant with regulations. Their primary responsibilities include the organization of clinical trial activities, the provision of information to participants, the management of data collection, and the assurance that the study adheres to the protocol.

The following are a few of the primary responsibilities of Clinical Research Coordinator positions:

• Managing the recruitment and vetting of participants.
• Overseeing regulatory compliance and study documentation.
• Conducting patient assessments and monitoring during clinical trials.
• Guaranteeing that all study activities adhere to FDA regulations and Good Clinical Practice (GCP).

Why Choose a Clinical Research Coordinator Career?

There are numerous advantages to pursuing a career in clinical research, particularly for those who are interested in the healthcare sector. The following are the reasons why Clinical Research Coordinator Jobs in the United States are an appealing choice:

• High Demand: The demand for clinical research professionals who are qualified is on the rise as the healthcare industry continues to expand. This implies that there is an abundance of Clinical Research Coordinator positions in the United States, with pharmaceutical companies, hospitals, research centers, and universities frequently recruiting CRCs.
• Career Development: Clinical research coordinators have the potential to advance to more senior roles, such as Clinical Research Associate (CRA) or Clinical Research Manager. You may also advance to positions such as Principal Investigator or Study Director with the appropriate level of experience.
• Competitive Salary: The average annual salary for clinical research coordinators, as reported by the Bureau of Labor Statistics, can vary from $50,000 to $90,000, contingent upon their location and level of experience. Specialized disciplines may yield higher annual salaries.
• Impactful Work: Coordination of clinical trials will place you at the forefront of medical advancements, enabling you to contribute to the development of novel treatments and therapies that enhance the quality of life for patients.

Key Qualifications:

In order to achieve success as a Clinical Research Coordinator in the United States, specific qualifications and abilities are necessary:

• Educational Background: A bachelor’s degree in life sciences, nursing, or a related field is typically required. Advanced degrees, such as a Master’s in Clinical Research, can provide an additional advantage.
• Certifications: Although not always required, certifications such as the Clinical Research Coordinator Certification from the Society of Clinical Research Associates (SoCRA) or the Certified Clinical Research Coordinator (CCRC) from the Association of Clinical Research Professionals (ACRP) can enhance your credibility and job prospects.
• Experience: It is frequently necessary to have experience in clinical research, medical settings, or working with patient data. While entry-level positions may be accessible, the majority of clinical research positions necessitate prior experience in a clinical research environment.
• Skills: The position requires a high level of attention to detail, strong organizational skills, and a comprehensive understanding of clinical trial regulations and GCP. Interacting with patients, researchers, and other stakeholders necessitates exceptional communication abilities.

How to Find Clinical Research Coordinator Jobs?

A proactive approach is necessary to locate Clinical Research Coordinator positions in the United States. To initiate the process, consider the following suggestions:

• Search Job Boards: Clinical Research Coordinator positions are frequently advertised on popular job boards such as Glassdoor, LinkedIn, and Indeed. Ensure that your search is narrowed to positions in the healthcare and clinical research sectors.
• Check Company Websites: Examine the websites of the organizations you are interested in: Numerous pharmaceutical companies, hospitals, and research institutions publish job opportunities directly on their websites. Keep a watch on these listings for the most recent opportunities.
• Network: Networking is essential for identifying job opportunities within the clinical research community. To broaden your network, participate in industry conferences, webinars, and establish connections with professionals on platforms such as LinkedIn.
• Cooperate with Recruiters: It is advisable to engage recruitment agencies that specialize in clinical research and healthcare positions. These agencies frequently maintain exclusive job listings and can assist you in obtaining employment.

Banner Health Careers:

What is the reason for your interest in collaborating with Banner Health? Naturally, it is an exceptional vocation in the healthcare sector and an exceptional location to reside in, regardless of one’s age. In the Western region, there is a healthcare profession that is suitable for all, from the small villages in the plains and mountains to the bustling cities of Phoenix.

Banner Health, one of the largest nonprofit health systems in the country, provides the opportunity to explore new regions of the country while also providing the security that is a result of success. Professionals who aspire to assume a significant position in an innovative organization can capitalize on numerous benefits.

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Conclusion:

For those who are passionate about healthcare, research, and having a positive impact on the lives of patients, jobs as clinical research coordinators in the United States offer a fulfilling career path. CRCs are essential in the advancement of medical research and treatment options, as they have access to a plethora of opportunities in pharmaceutical companies, research institutions, and hospitals. The initial step toward a fulfilling career in the field of clinical research can be achieved by securing a position as a clinical research coordinator.

Frequently Asked Questions: