clinical allergist

United Allergy Services

<div>Be part of our team of Clinical Allergy Specialists making a difference in the lives of allergy sufferers!
Are you seeking a medical career opportunity where you make a real difference in patient lives? Do you enjoy patient interaction? Are you looking for a work environment that promotes career growth? If so, join our team of Clinical Allergy Specialists!
Who we are:
At United Allergy Services, we partner with practitioners in over 18 states to provide on-site allergy testing and treatment options, aiming to revolutionize allergy care and expand access to millions who would otherwise go without it.
Your future role:
As a Clinical Allergy Specialist, you will play a crucial role in our mission to provide accessible allergy care by administering allergy tests and injections, educating patients on immunotherapy, and driving the growth of the allergy center within a partnered practice.
Key responsibilities:<ul><li>
Administer allergy tests and injections under a supervising physician.</li><li>
Prepare customized patient immunotherapy vials.</li><li>
Educate and support patients through their immunotherapy treatment journeys.</li></ul><ul><li>
Complete basic administrative tasks such as scheduling appointments and handling medical documentation.</li><li>
Collaborate with healthcare providers to deliver exceptional allergy care and treatment.</li><li>
Coordinate within the clinic to create visibility and presence for the allergy services.</li></ul>
Qualifications:<ul><li>
A Bachelor of Science degree in health-related fields is preferred, however a combination of health-related education and experience will be considered.</li><li>
A minimum of 1 year full-time clinical experience, medical office setting, customer service, or similar industry is preferred.</li><li>
Strong communication, interpersonal, organizational, and time management skills required.</li><li>
User experience with medical office and/or business software programs are preferred.</li></ul>
Benefits:<ul><li>
Paid: Time off, holidays, and training.</li><li>
Medical, dental, vision, and life insurance are available.</li><li>
Generous 401(k) retirement plan with company match.</li><li>
Performance-based bonuses, company contest rewards, and employee/client referral bonuses.</li><li>
On-site and remote training/support for allergy care provided.</li><li>
Career advancement opportunities.</li><li>
Employee Assistance Program (EAP)</li><li>
Daytime, business week schedule. No holidays, no weekends (unless required by the clinic).</li><li>
Pay range: $20-23/hr</li><li>
#UAS2</li></ul></div>

Clinical Allergy Specialist

Keiser University

<div>The Clinical Coordinator position plans, coordinates, facilitates, administers, and monitors, activities on behalf of the academic program and in coordination with academic and clinical faculty. These activities ensure the quality of our students learning experience during clinical education. Clinical Coordinators accomplish this through: 
<ul><li>
Assists with the development and assessment of the clinical education component of the curriculum with the Program Director.</li><li>
Coordination and implementation of the clinical education component of the curriculum including site placements, site visits, and evaluation.</li><li>
Responsible for facilitating students' clinical education.</li><li>
Responsible for ensuring clinical education program compliance.</li></ul><h1 class="jobSectionHeader"> 
EDUCATION, EXPERIENCE AND TRAINING:</h1><ul><li>
Minimum of a bachelor's degree</li><li>
At least 2 years of clinical practice experience as an occupational therapist or occupational therapy assistant (ACOTE Standards).</li><li>
Current, unrestricted Florida licensed occupational therapist or occupational therapy assistant.</li></ul></div>

Clinical Coordinator- OTA (Academic Fieldwork Coordinator)

Sunrise Research Institute

About 3Sync Research3Sync Research is a growing clinical research organization dedicated to advancing medicine through high-quality clinical trials. We partner with leading pharmaceutical companies, CROs, physicians, and healthcare professionals to bring innovative treatment options to diverse patient populations.Our office conducts outpatient clinical research across multiple therapeutic areas, including primary care, pediatrics, asthma/allergy, diabetes, endocrinology, infectious disease, vaccines, and other adult and pediatric studies. We are looking for a strong, experienced provider who is comfortable working directly with patients and supporting clinical trial oversight.Position OverviewWe are seeking a bilingual APRN / Nurse Practitioner to join our clinical research team as a Clinical Trial Sub-Investigator. This is an excellent opportunity for an experienced provider who is detail-oriented, and comfortable working with both adults and children.In this role, you will work closely with the Principal Investigator, site directors, operations leadership, recruitment team, clinical research coordinators, sponsors, CROs, and regulatory teams to support the safe and compliant conduct of clinical trials. The Sub-Investigator will conduct patient screening, eligibility review, physical exams, safety assessments, protocol compliance, clinical documentation, enrollment support, participant retention, and contribute to overall site performance.Key ResponsibilitiesAssist the Principal Investigator in the oversight and execution of clinical trialsConduct patient screening, enrollment, and ongoing study visit assessmentsPerform physical exams and clinical evaluations for adult and pediatric participantsReview medical history, medications, labs, vitals, inclusion/exclusion criteria, and study eligibilityMonitor participant safety throughout the studyIdentify, assess, document, and report adverse events and clinical concernsPerform or assist with blood draws, vital signs, and other protocol-required proceduresReview informed consent forms, source documents, lab reports, CRFs, and study records for accuracy and completenessSupport protocol compliance, data collection, and audit readinessCommunicate professionally with participants, parents/guardians, study staff, sponsors, CROs, and regulatory teamsSupervise and support clinical research staff when neededCollaborate closely with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to support successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performanceServe as a team player within a fast-paced clinical research environment, helping ensure smooth communication between clinical, operational, and recruitment staffEnsure study activities are conducted in compliance with FDA regulations, ICH-GCP guidelines, HIPAA, protocol requirements, and site SOPsRequirementsActive and unrestricted License/Certification- Florida APRN / Nurse Practitioner License requiredMinimum of 5+ years of experience as an APRN / Nurse Practitioner(Bilingual English/Spanish )Must be comfortable working with both adult and pediatric patientsStrong clinical assessment, documentation, and decision-making skillsExperience with patient evaluation, medical history review, medication review, labs, and clinical proceduresPhlebotomy or blood sampling experience preferredFamiliarity with medical terminology, clinical documentation, and outpatient patient careAbility to work independently while collaborating with the Principal Investigator and research teamStrong attention to detail and ability to work in a fast-paced clinical environmentProfessional, dependable, organized, proactive, and team-orientedGCP certification preferred; training can be provided if neededAvailability to work occasional weekends as needed based on study requirementsPreferred ExperienceFamily MedicinePrimary CarePediatricsInternal MedicineUrgent CareAllergy / AsthmaEndocrinologyDiabetes CareInfectious DiseaseVaccinesClinical ResearchClinical Trial Sub-Investigator experienceIdeal CandidateThe ideal candidate is an experienced, bilingual provider who is comfortable making clinical assessments, asking the right questions, identifying safety concerns, and working with a wide range of patients. We are looking for someone who is confident in their clinical judgment, reliable, personable, and able to take ownership of patient evaluations in a research setting.This person should also be a strong team player who works well with site directors, operations leadership, recruitment teams, coordinators, and the Principal Investigator to help drive successful study outcomes, strong enrollment, participant retention, protocol compliance, and overall site performance.Why Join 3Sync ResearchOpportunity to work on innovative clinical trials and emerging treatmentsAdult and pediatric patient populationGrowing research organization with expanding study opportunitiesCollaborative team environmentExposure to multiple therapeutic areasFlexible schedule availableMeaningful role in supporting patient safety and advancing clinical researchBenefits:Health insuranceDental insuranceVision insurancePaid time offPay: $88,117.74 - $106,120.29 per yearBenefits:<ul><li>Dental insurance</li><li>Health insurance</li><li>Paid time off</li><li>Vision insurance</li></ul>Work Location: In person

Bilingual APRN / Nurse Practitioner

Huntsville Hospital Health System

<div>Overview:
<div>
Reporting to the manager, clinical informatics, the clinical informaticist is the hospital liaison for clinical informatics to the Medical Staff, Pharmacy and other Clinical Departments. Responsibilities will include: Physician systems orientation, CPOE execution, on-boarding, training and meaningful use compliance.
</div>Qualifications:
<div>
Education: BSN required. Degree in clinical informatics or RNBC (Board Certified by the ANCC in nursing informatics) preferred.</div><div>
License: Alabama Board of Nursing RN Degree &ndash; preferred. Current RNBC if no degree in clinical informatics, preferred.</div><div>
Experience: Clinical work practice, Clinical Information Systems implementation, oversight or programming, Other positions requiring Medical Staff relationships and project development. Management experience.</div></div>

Clinical Informatics Specialist-Technical Services-FT-1st shift

Piper Companies

<div>
 
 Piper Companies
 
 is looking for an
 
 In-House Clinical Research Associate
 
 to join a clinical research company located in
 
 Bethesda, MD.
 
 
 
 
 Responsibilities of the In-House Clinical Research Associate include:
 
 
 
 <ul>
 <li>
 Review and process essential regulatory documents received from clinical trial sites
 </li>
 <li>
 Request missing or additional documentation and respond to protocol or process-related inquiries
 </li>
 <li>
 Maintain and organize Trial Master Files (TMF) and centralized document systems
 </li>
 <li>
 Track regulatory documents and workflow in a centralized web-based system or database
 </li>
 <li>
 Ensure documents meet FDA, ICH GCP, and sponsor requirements for accuracy and completeness
 </li>
 <li>
 Troubleshoot regulatory document issues and follow up with study sites as needed
 </li>
 <li>
 Support distribution of trial-related materials and assist with study team coordination
 </li>
 <li>
 Assist with monitoring visit preparation and follow-up, including teleconference coordination
 
 
 </li>
 </ul>
 
 Qualifications for the In-House Clinical Research Associate include:
 
 
 
 <ul>
 <li>
 3&ndash;5 years of experience in a clinical research setting
 </li>
 <li>
 Experience with regulatory document review/collection and knowledge of FDA and ICH GCP guidelines
 </li>
 <li>
 Experience with eTMF systems (e.g., Veeva Vault) and system administration skills
 </li>
 <li>
 Experience with Trial Master Files and centralized tracking systems
 </li>
 <li>
 Experience with IRB submissions and OHRP regulations is a plus
 </li>
 <li>
 Bachelor&rsquo;s degree required
 </li>
 <li>
 Strong organizational, communication, and time management skills
 </li>
 <li>
 Proficiency with Microsoft Office (Word, Excel, Outlook)
 
 
 </li>
 </ul>
 
 Compensation for In-House Clinical Research Associate includes:
 
 
 
 <ul>
 <li>
 Rate Range: $50,000&ndash;$80,000, depending on experience
 </li>
 <li>
 Comprehensive Benefit Package: Cigna Medical/Dental/Vision, 401K, Sick Leave as Required by Law
 
 
 </li>
 </ul>
 
 This job is open for applications on June 1st, 2026. Applications will be accepted at least 30 days from the posting date.
 
 
 
 Keywords: Clinical Research, Clinical Trials, Clinical Operations, In-House CRA, TMF, Trial Master File, eTMF, Veeva Vault, Regulatory Documents, Regulatory Affairs, Document Management, ICH GCP, FDA Regulations, Good Clinical Practice, Essential Documents, Site Document Collection, IRB Submissions, OHRP Regulations, Site Start-Up, Study Coordination, Clinical Study Support, Monitoring Support, TMF Maintenance, Document Tracking, Compliance, Audit Readiness, Clinical Data Management, Sponsor Oversight, CRO, Protocol Compliance, Investigator Communication, Site Management, Clinical Systems, Database Tracking, Microsoft Excel, Microsoft Word, Microsoft Outlook
 
 
</div>

In-House Clinical Research Associate

Combined Health Center Corp

Job Overview We are seeking a dynamic and detail-oriented Research Coordinator/Medical Assistant to join our clinical research team. This role is vital in coordinating and supporting clinical trials, ensuring compliance with regulatory standards, and providing exceptional patient care. The ideal candidate will possess a strong foundation in medical terminology, clinical procedures, and research protocols, with a passion for advancing medical knowledge through meticulous data collection and management. This paid position offers an exciting opportunity to contribute to groundbreaking research projects while developing your skills in clinical development and regulatory compliance.Duties<ul><li>Assist in the planning, organization, and execution of clinical trials, ensuring adherence to study protocols and regulatory guidelines such as FDA regulations and ICH GCP standards</li><li>Conduct patient monitoring by taking vital signs, performing blood sampling (phlebotomy), and documenting clinical observations accurately within electronic medical records (EMR) systems</li><li>Review and verify study documentation for accuracy, completeness, and compliance with protocol requirements</li><li>Manage data collection, entry, and management using statistical software and CDISC standards to ensure high-quality data integrity</li><li>Support clinical laboratory procedures, including specimen handling and processing, while maintaining strict compliance with HIPAA privacy regulations</li><li>Supervise or assist with research staff training on Good Clinical Practice (GCP) and study-specific procedures</li><li>Monitor patient safety throughout the trial process, including adverse event reporting and compliance management</li><li>Collaborate with investigators, sponsors, and regulatory bodies to ensure smooth trial operations and adherence to all applicable guidelines</li></ul>Experience<ul><li>Proven supervising experience in a clinical or research setting, demonstrating leadership in managing teams or projects</li><li>Hands-on experience managing clinical trials from initiation through closeout phases</li><li>Strong knowledge of medical terminology, clinical laboratory procedures, and blood sampling techniques (phlebotomy)</li><li>Familiarity with EMR systems, data management tools, statistical software, and CDISC standards for data collection and analysis</li><li>Understanding of FDA regulations, ICH GCP guidelines, HIPAA privacy rules, and clinical development processes</li><li>Certification in Good Clinical Practice (GCP) from a recognized issuer such as the ICH GCP certificate or equivalent is required; valid certification for California (CA) preferred</li><li>Experience working within clinical research environments involving blood sampling, vital signs assessment, and patient monitoring</li><li>Ability to review complex documentation meticulously while maintaining high standards of compliance and accuracy</li></ul>Join us in advancing innovative healthcare solutions! This role offers the chance to work at the forefront of clinical research while honing your skills in a collaborative environment dedicated to excellence. We value motivated professionals eager to make a difference through meticulous research practices combined with compassionate patient care.Pay: $35,500.96 - $50,000.00 per yearWork Location: In person

Research Coordinator/ Medical Assistant

Elevate Clinical Research

<div>About Company:
Elevate Clinical Research is a mission‑driven organization expanding access to high‑quality clinical trials across Texas, Louisiana, Illinois, Maryland, Kansas, and growing. We exist to bring research closer to the communities that need it most, delivering compassionate patient care, operational excellence, and trustworthy data that advances medicine.
At Elevate, your work has real impact. Every role contributes directly to improving health outcomes and bringing new therapies to life. We hire people who care deeply about patients, believe in doing things the right way, and want to grow with a company that&rsquo;s expanding nationwide.
What We Value<ul><li>
Patients first in every decision and interaction</li><li>
Access, equity, and bringing research to underserved communities</li><li>
High‑quality, compliant, reliable study execution</li><li>
Purpose‑driven growth and opportunities for advancement</li><li>
Supportive teams who communicate, collaborate, and care</li></ul>
Why People Join Us<ul><li>
A mission that matters</li><li>
Clear, structured onboarding</li><li>
Leadership that listens and supports</li><li>
Career growth as we expand into new states</li><li>
A culture built on integrity, teamwork, and accountability</li></ul>
Join Elevate and help build a patient‑centered research network that&rsquo;s changing what clinical trials can look like for communities across the country.
About the Role:
The Clinical Research Coordinator (CRC) plays a pivotal role in the successful execution and management of clinical trials within healthcare settings. This position is responsible for coordinating all aspects of clinical research studies, ensuring compliance with regulatory requirements and institutional policies. The CRC serves as a liaison between investigators, study sponsors, and participants, facilitating effective communication and smooth study progression. By meticulously managing patient recruitment, data collection, and study documentation, the CRC ensures the integrity and quality of clinical research data. Ultimately, this role contributes to advancing medical knowledge and improving patient care through the rigorous conduct of clinical research.
Minimum Qualifications:<ul><li>
Bachelor&rsquo;s degree in a health-related field such as Nursing, Life Sciences, or Public Health.</li><li>
At least 2 years of experience coordinating clinical research studies or trials.</li><li>
Comprehensive knowledge of clinical trial processes, regulatory requirements, and ethical standards.</li><li>
Familiarity with clinical research documentation, including informed consent forms and case report forms.</li><li>
Strong organizational skills and attention to detail to manage multiple study activities simultaneously.</li></ul>
Preferred Qualifications:<ul><li>
Certification as a Clinical Research Coordinator (e.g., ACRP-CRC or SOCRA).</li><li>
Experience working with electronic data capture (EDC) systems and clinical trial management systems (CTMS).</li><li>
Advanced knowledge of FDA regulations and Institutional Review Board (IRB) processes.</li><li>
Previous experience in patient recruitment and retention strategies for clinical studies.</li><li>
Master&rsquo;s degree in Clinical Research, Public Health, or a related discipline.</li></ul>
Responsibilities:<ul><li>
Coordinate and oversee the daily operations of clinical trials, including patient recruitment, informed consent, and scheduling study visits.</li><li>
Ensure compliance with all regulatory requirements, institutional policies, and Good Clinical Practice (GCP) guidelines throughout the study lifecycle.</li><li>
Maintain accurate and up-to-date regulatory documents, case report forms, and study databases to support data integrity and audit readiness.</li><li>
Monitor study progress and patient safety by conducting regular assessments and reporting adverse events to the appropriate parties.</li><li>
Collaborate with investigators, sponsors, and multidisciplinary teams to facilitate effective communication and resolve study-related issues promptly.</li></ul>
Skills:
The required skills such as clinical trials coordination, regulatory document management, and patient recruitment are essential for ensuring that studies are conducted efficiently and ethically. Clinical monitoring and trial management skills enable the coordinator to oversee study progress and maintain compliance with protocols and regulations. Proficiency in clinical research and clinical practice allows the coordinator to understand medical terminology and patient care considerations, facilitating effective communication with healthcare providers and participants. Preferred skills like experience with electronic data systems and advanced regulatory knowledge enhance the ability to manage complex data and navigate regulatory landscapes. Together, these skills support the daily responsibilities of maintaining study integrity, safeguarding participant safety, and contributing to the advancement of healthcare research.</div>

Clinical Research Coordinator

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