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The entire PCM Trials team is committed to  helping create positive experiences and assuring data quality for patients, sites, sponsors, and CROs. PCM Trials’ Certified Mobile Research Nurses ( CMRNs ) focus on patients. Working with clinical study participants outside traditional site visits, we enable patients to access clinical research care options that might otherwise not be accessible. While we most often see patients in their homes, we also serve patients in school, on vacation, in long-term care facilities, or at work – even backstage at a Broadway show. CMRNs’ mobile research visits  reflect the broad scope of clinical research in terms of patients, therapeutic areas, and procedures.

Beyond individual study participants, our CMRNs can ultimately improve care for thousands of patients – or even millions – by supporting the development of next-generation therapeutics. From rare diseases and cancer to some of the most prevalent conditions, CMRNs play a critical role in developing new treatments.

Whether you have years of research experience or are looking to expand your professional horizons, PCM Trials is committed to matching you with research studies that will build on your strengths and open new opportunities for growth. We support your success through our CMRN testing and continuing education as well as protocol-specific training. Our goal is that every patient encounter will be a positive one – for the patient, the CMRN, the research site, and the study sponsor.   We live Our Values every day.

Certified Mobile Research Nurses

The entire PCM Trials team is committed to Our Values , which guide our work every day, helping create positive experiences and assuring data quality for patients, sites, sponsors, and CROs. PCM Trials’ Certified Mobile Research Nurses ( CMRNs ) focus on patients. Working with clinical study participants outside traditional site visits, we enable patients to access clinical research care options that might otherwise not be accessible. While we most often see patients in their homes, we also serve patients in school, on vacation, in long-term care facilities, or at work – even backstage at a Broadway show. CMRNs’ mobile research visits reflect the broad scope of clinical research in terms of patients, therapeutic areas, and procedures.

Whether you have years of research experience or are looking to expand your professional horizons, PCM Trials is committed to matching you with research studies that will build on your strengths and open new opportunities for growth. We support your success through our CMRN testing and continuing education as well as protocol-specific training. Our goal is that every patient encounter will be a positive one – for the patient, the CMRN, the research site, and the study sponsor.

I love being a CMRN because it’s a great PRN job while working full- or part-time.   I get to make my own schedule and be very autonomous. Yet when I need help, the team is always responsive and supportive. – CMRN

I enjoy traveling locally (and sometimes beyond) and building relationships with study participants and their families while performing visits. It’s also very rewarding to be a part of advancing innovative treatments through clinical research. – CMRN

If you are a registered nurse who wants to help individuals and expand your impact, click below to explore CMRN opportunities today.

Career Opportunities

Operations Support

Our CMRNs set the standard for mobile research nursing, but they do not do it alone. They are backed by some of the best clinical operations support professionals in the industry. Whether conducting site initiation visits or ensuring that CMRNs have the logistical support they need – including the right investigational products and supplies for each visit – our clinical operations team helps deliver a superior patient experience and quality data for sponsors.

If you want to contribute to advancing clinical research and making sure patients have access to the latest medical breakthroughs, click below to learn more about operations support career opportunities.

PCM Trials Values

When you join PCM Trials you become part of a team that is leading the way in mobile research and decentralized trials.   We live Our Values every day.

Professional Case Management is an equal opportunity employer that evaluates all qualified applicants without regard to race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

Are you interested in becoming part of our clinical or corporate team?

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Nurse Practitioner

🔍 school of medicine, stanford, california, united states.

Stanford University, Department Pediatrics, Division of Infectious Diseases is seeking a part time (50%) Nurse Practitioner – Research to apply medical knowledge and experience, under the direction of the principal investigator to oversee and direct clinical course of research participants in clinical trials. Assess physical health and administer treatments throughout the study aligned with scope of practice and delegated responsibilities. Oversee study conduct and assure study participant safety. Coordinate and manage care for participants enrolled in a clinical research trail, responsibilities will include preparation and submission of protocol related documents and amendments to the IRB, FDA and Sponsors, identify and recruitment of participants, obtaining informed consent, management of protocol related finances to include   the study workbook and ensure billing compliance, perform phlebotomies and insertion of IVs, perform skin prick tests, prepare and maintain source documentation for phase 1-3 studies. Participate in study design, communicate with families, participants referring physicians and other health care providers, teaching and advice to participants and families to ensure compliance and retention of study participants, tracking and recording of adverse events, perform physical exams to ensure enrollment criteria and to track for any changes during study participation, formulate and evaluate treatment plans, be available for on call advice and emergencies between clinic visits, administer rescue medications based on clinical judgment, write develop and maintain database of clinical trial information, assist in analysis of study data.

Duties include:

·         Ensure the safety of study participants, and maintain communication with their families/caregivers and clinicians.

·         Provide clinical and administrative medical support and oversight for research clinical trials based on scope of practice; obtain complete study participant history, conduct physical exams, review medical charts, assess findings, prescribe and re- fill medication, and perform designated procedures according to written protocols.

·         Collaborate with clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols.

·         Assess, grade, and document adverse events; apply triage and judgment to determine course of action.

·         Oversee and, as needed, administer medications and treatments per study protocol and scope of practice.

·         Comply with institutional policies, standard operating procedures, and guidelines; prepare and submit documentation as required by the study protocol and study sponsor; interpret complex protocols and regulatory requirements.

·         Coordinate and collaborate with principal investigator to review study protocol; assess and analyze feasibility, budget projections, and staffing needs.

·         Supervise and train non- clinical and clinical staff/students, as needed.

·         Identify, recruit, and enroll study participants, as well as maintain study participant records; determine study participant criteria.

·         Support sponsor investigator research with investigational new drug/investigational device exemption applications.

• - Other duties may also be assigned

Stanford University provides pay ranges representing its good faith estimate of what the University reasonably expects to pay for a position. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location and external market pay for comparable jobs. The pay range for this position working in the California Bay area is between $52,600 to $78,490 based on commensurate experience and background.

DESIRED QUALIFICATIONS:

• Knowledge of GCP, ICH and FDA regulatory (CFR Title 21 part 312)
• Experience overseeing outpatient clinical research studies
• NPF licensure

EDUCATION & EXPERIENCE (REQUIRED):

Bachelor's degree, Nurse Practitioner license and three years of relevant experience, or combination of education and relevant experience.

KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):

• Ability to provide work direction to research support staff
• Demonstrated understanding of good clinical practices and regulatory compliance.
• Demonstrated ability to perform the functions of the position with minimal supervision.
• Verbal and written communication skills to convey medical and research-related information to research subjects of all ages and backgrounds.
• Ability to identify confidential and sensitive information (written and verbal).
• Ability to implement good clinical practices in all interactions with study participants, their families, and colleagues.
• Ability to identify adverse reactions to study treatments and perform the required study protocol documentation to record these activities
• Ability to implement study protocols with minimal supervision.

CERTIFICATIONS & LICENSES:

• Licensed as a Registered Nurse by the California State Board of Registered Nursing. Certified as Nurse Practitioner by the California State Board of Registered Nursing. Must include a Nurse Practitioner Furnishing Number
• Current basic CPR certification.

PHYSICAL REQUIREMENTS*:

• ·         Frequently stand/walk, sit, perform desk-based computer tasks, twist/bend/stoop/squat, grasp lightly/fine manipulation, use a telephone, write by hand, and sort/file paperwork or parts.
• Occasionally reach/work above shoulders, grasp forcefully, operate foot and/or hand controls.
• Rarely kneel/crawl, climb (ladders, scaffolds, or other), scrub/sweep/mop/chop/mix, operate a manual pipette.
• Ability to obtain and maintain a valid California non-commercial class license and operate vehicle during daylight  hours.

*   - Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.

WORKING CONDITIONS:

• May be required to work with, take specific precautions against, and/or be immunized against potentially hazardous agents.
• May be exposed to blood borne pathogens.
• On call 24 hours/day.
• Occasional travel for research meetings and conferences likely

~ All members of the Department of Pediatrics are engaged in continuous learning and improvement to foster a culture where diversity, equity, inclusion, and justice are central to all aspects of our work. The Department collectively and publicly commits to continuously promoting anti-racism and equity through its policies, programs, and practices at all levels. ~

• Schedule: Part-time
• Job Code: 4568
• Employee Status: Regular
• Department URL: http://pediatrics.stanford.edu/
• Requisition ID: 103672
• Work Arrangement : Hybrid Eligible

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