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Hiring remote Field Clinical Engineers/Specialists in the Souththeast region of the USA. About Recor Medical At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise™ uRDN System, we are on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe. Position Summary: The primary purpose of the Clinical Field Specialist role is to build a clinical patient pipeline for Recor-sponsored clinical studies. This role partners with clinical sites to expand the referral base and drive patient recruitment through targeted, data-driven outreach and education. The Field Clinical Specialist also provides procedure support including case proctoring, physician certifications, and site qualification visits. Responsibilities and Duties Drive Provider Referral Program: • Analyze claims and EMR data to identify high-potential providers and patient populations., • Develop and execute targeted outreach and education programs with site teams. Guide EMR Patient Identification & Reporting: • Collaborate with investigators and research coordinators to define and validate EMR flagging criteria; provide hands-on support to sites for implementing and optimizing flags within their systems., • Collaborate with site teams to generate targeted patient lists for chart review by leveraging EMR data and predefined eligibility criteria. Procedure & Training Leadership: • Proctor cases and certify physicians on protocol and device use; deliver hands-on training and maintain compliance records. Site Qualification & Activation: • Plan and conduct Site Qualification Visits (SQV) and Site Initiation Visits (SIV) with CRA/PM to ensure activation requirements are met and Day-1 recruitment workflows are ready. Cross-Functional Problem Solving: • Collaborate with Clinical Ops, Medical Affairs, Quality/Regulatory, and Commercial teams to remove enrollment barriers and improve site performance. Requirements: • Bachelor’s degree in Life Sciences, Nursing, or related field., • 4+ years' experience in clinical research, site management, or field clinical support., • Strong knowledge of GCP, FDA regulations, and cardiovascular procedures., • Proven ability to lead training programs and manage complex site workflows., • Excellent communication, data interpretation, and relationship-building skills. Preferred Qualifications: • Clinical Research Coordinator (CRC) certification or equivalent clinical research training, • Experience as a Field Clinical Engineer or similar technical role., • IDE trial experience and hypertension knowledge., • Proficiency with EMR systems and clinical trial platforms. Salary range: $121K - $150K (Annual Base Salary) (Commensurate with experience, skills, education, and training) Pre-Employment Requirement At Recor Medical, patient safety and compliance are at the heart of everything we do. To support these standards, employment for all field-based roles is contingent upon successfully completing a pre-employment background check and drug screen. These steps help ensure we bring the highest level of integrity and accountability to the physicians and patients we serve. Radiation Safety Requirement Certain field-based roles at Recor Medical require work in environments where radiation sources (e.g., x-ray equipment) are in use. Employees in these roles will be issued a personal dosimetry badge to monitor occupational exposure and are required to wear it in accordance with company policy and applicable regulatory standards. This program is designed to ensure compliance with federal and state regulations and to maintain radiation exposure at levels that are As Low As Reasonably Achievable (ALARA). Additional guidance and protective equipment, as necessary, will be provided as part of onboarding and ongoing safety training. About Recor Medical At Recor Medical, we are pioneering Ultrasound Renal Denervation (uRDN) therapy to treat hypertension, the leading cardiovascular risk factor in the world. With our Paradise™ uRDN System, we are on a mission to provide the millions of people who suffer from hypertension with a non-drug and minimally invasive option to lower their blood pressure. Join us on our journey and make a meaningful impact on the lives of people around the globe. Position Summary: The primary purpose of the Clinical Field Specialist role is to build a clinical patient pipeline for Recor-sponsored clinical studies. This role partners with clinical sites to expand the referral base and drive patient recruitment through targeted, data-driven outreach and education. The Field Clinical Specialist also provides procedure support including case proctoring, physician certifications, and site qualification visits. Responsibilities and Duties: Drive Provider Referral Program: • Analyze claims and EMR data to identify high-potential providers and patient populations., • Collaborate with investigators and research coordinators to define and validate EMR flagging criteria; provide hands-on support to sites for implementing and optimizing flags within their systems., • Collaborate with site teams to generate targeted patient lists for chart review by leveraging EMR data and predefined eligibility criteria. Procedure & Training Leadership: • Proctor cases and certify physicians on protocol and device use; deliver hands-on training and maintain compliance records. Site Qualification & Activation: • Plan and conduct Site Qualification Visits (SQV) and Site Initiation Visits (SIV) with CRA/PM to ensure activation requirements are met and Day-1 recruitment workflows are ready. Cross-Functional Problem Solving: • Collaborate with Clinical Ops, Medical Affairs, Quality/Regulatory, and Commercial teams to remove enrollment barriers and improve site performance. Requirements: • Bachelor’s degree in Life Sciences, Nursing, or related field., • 4+ years' experience in clinical research, site management, or field clinical support., • Strong knowledge of GCP, FDA regulations, and cardiovascular procedures., • Proven ability to lead training programs and manage complex site workflows., • Excellent communication, data interpretation, and relationship-building skills. Preferred Qualifications: • Clinical Research Coordinator (CRC) certification or equivalent clinical research training, • Experience as a Field Clinical Engineer or similar technical role., • IDE trial experience and hypertension knowledge., • Proficiency with EMR systems and clinical trial platforms. Salary range: $121K - $150K depending on location and experience. The successful candidate's starting base pay will be determined based on job-related skills, experience, qualifications, work location and market conditions. The expected base pay range for this role may be modified based on market conditions.

The Division of Pediatric Gastroenterology and Nutrition seeks a ninth pediatric gastroenterologist to join a growing academic and clinical division! The position provides an exciting opportunity to pursue an active academic career in pediatric gastroenterology and nutrition. Physicians interested in Advanced Endoscopy experience (i.e., ERCP with sphincterotomy and stent placements, Endoscopic Ultrasound with Fine needle aspiration, double balloon enteroscopy, endoscopic submucosal dissection, POEM, G-POEM, Endoknife, Transnasal Endoscopy) are encouraged to apply. Physicians with a passion for undergraduate and graduate medical education and wanting to partner in the establishment of a pediatric gastroenterology fellowship program are also encouraged to apply. Current faculty is comprised of 8 pediatric gastroenterologists, two of which are primarily affiliated with a partner hospital. Four full time nurse practitioners, 2 registered dietitians, 1 research coordinator, 2 social workers/licensed clinical therapists, 2 clinical coordinators and 1 family support and advocacy coordinator play integral roles in our vibrant and busy division. We are supported by the presence of all major pediatric subspecialists. We have an integrated and coordinated GI/Surgery program alignment, with specific focuses on Motility, Polyposis, Short Gut/Intestinal Rehabilitation and Inflammatory Bowel Disease. Imbedded in the GI Division are Centers dedicated to Feeding Disorders, Celiac Disease, Inflammatory Bowel Disease, Intestinal Rehabilitation and complex Motility disorders. In addition, the Division has a long standing clinical and research interest in Disorders of Brain-Gut Interactions, Celiac disease, and Eosinophilic Gastrointestinal Diseases. Our division plays an integral part in the multidisciplinary care of patients with cystic fibrosis and Aerodigestive disorders. Responsibilities of these positions include providing direct patient care in inpatient and ambulatory settings, medical education of students and trainees, and participation in clinical research and/or quality improvement. The start date is negotiable, and the position will remain open until filled. The successful candidate will have experience and knowledge of all pediatric GI and hepatology disorders; demonstrated skills in the full gamut of pediatric GI endoscopic and other procedures; and excellent communication and team skills. The candidate will have completed fellowship in good standing in Pediatric Gastroenterology at RRC-approved fellowship program (or equivalent), MD (or equivalent) degree, Board Certified in Pediatrics, and BE/BC in Pediatric Gastroenterology.

This role requires strong clinical assessment abilities, adherence to regulatory standards, and the capacity to work both independently and collaboratively in a fast-paced clinical research environment. Perform clinical tasks within the nursing scope of practice to support physicians, ARNPs, and Cli

Job Description Insight Global is hiring a Clinical Research Coordinator for a large healthcare client in Orlando, Florida! Monday-Friday, 9am-5pm. No weekends, or holiday! Offering a competitive base salary and great benefits. JOB DESCRIPTION • Delivers safe care and demonstrates regard for the dignity and respect of all participants., • Maintains clinical competencies including physical assessment, phlebotomy, and IV insertion., • Practices the principles of Universal Precautions and understands HIPAA regulations., • Ability to perform clinical tasks including assisting physician, ARNP and CRN with minor procedures and other study requirements within scope of practice., • Ability to work independently in a fast-paced clinical or research environment, handling multiple tasks simultaneously, effectively, and in an organized and timely manner Demonstrated skills in clinical competencies including physical assessment, phlebotomy, IV insertion and administration of investigational drugs in accordance with AdventHealth Policies and Procedures. REQUIRED SKILLS AND EXPERIENCE • Associate’s degree Nursing, • ACLS + BLS, • CCRC: SOCRA or ACRP Accreditation NICE TO HAVE SKILLS AND EXPERIENCE • Bedside RN w/ Critical Care + Cardio experience, • Bilingual, • Additional RN certifications – CCRN, Transplant, etc.

Job Description K2 is pooling for a Prescreen Coordinator to support our clinic in Maitland, FL. The Prescreen Coordinator promotes Good Clinical Practice in the conduct of reviewing of medical information to ensure patients are qualified for current or potential studies. Disclaimer: We are constantly growing and looking for passionate individuals to help us reach new heights. This posting serves as a talent pipeline for upcoming roles; we encourage you to submit your application so we can reach out when an opening aligns with your expertise and our mission. Responsibilities: • Triage patients to determine eligibility for active and/or potential studies, • Conduct psychiatric intakes, • Collect initial medical and psychiatric information by interviewing patients and obtaining medical records, • Perform clinical tasks included, but not limited to, memory testing, vital signs, height and weight, • Assist CRCs with patient care and data management, • Thoroughly understand all assigned studies through reading protocols, attending investigator meetings, start-up meetings, and coordinating with principal investigator, • Educate patients and family regarding the details, requirements, and risks of the clinical trial, • Schedule screens and follow up appointments, • Enter all pre-screen test results, medical conditions and medications into database, • Tracking all data through database and all trackers within assuring all data is entered and up to date, • Excellent customer service skills, • Professional and friendly phone manner, • Excellent computer data entry skills, • Ability to work in fast paced environment, • Ability to handle multiple tasks, • Must be dependable, responsible & punctual, • Medical knowledge a plus, but not necessary, • Minimum Associates degree in mental health counseling, social work, or psychology highly desired, • Medical, Dental, Vision, Flexible Spending Accounts, Employer paid Long-Term disability and Life Insurance, Short Term Disability, Accident and Critical Illness Insurance, Voluntary Life and Long-Term Care Insurance, Legal Shield, Employee Assistance Program, and various discount programs., • 401(K) Plans- Traditional and Roth plans are available; 4% employer match that is immediately vested, • PTO of 16 days per year, 17 days after the first year of FT employment, • 9 paid Holidays We celebrate what makes you uniquely you! Your race, color, religion, marital status, age, national origin, or even your favorite snack (though we're partial to good research snacks) don't define your talent or fit here. If you need a little extra support or accommodation due to a disability, no sweat! Just reach out to our friendly team at , and we'll ensure you have everything you need to shine.

Job Description Job Title: Clinical Research Coordinator Location: Orlando, Florida Job Type: Full-time This is an onsite position in Orlando We are hiring a Clinical Research Coordinator for the Orlando Office. The Research Coordinator will be responsible to lead the growth and development of the research program while also working with other clinic staff on existing and new clinical trials. As part of CVAUSA’s national network, the Clinical Research Coordinator will have the opportunity to collaborate with teams across the country, making an impact on cardiovascular care both locally and nationwide. Position Overview: As a Clinical Research Coordinator you will play a key role in managing and overseeing all aspects of clinical trials and site operations. You will have the opportunity to take ownership of your projects, driving them forward with innovation, efficiency, and excellence. This is a fantastic opportunity for an ambitious, goal-oriented individual who thrives in an independent, fast-paced environment. Key Responsibilities: * Clinical Trial Management: Oversee all aspects of clinical trials, including patient recruitment, screening, and enrollment. Ensure that protocols are followed meticulously. * Site Operations: Handle day-to-day site management, ensuring that all activities comply with regulatory requirements and study protocols. * Data Management: Collect, verify, and manage clinical trial data, ensuring it is accurate and complete. * Communication & Reporting: Act as the primary point of contact for study sponsors, participants, and other stakeholders. Provide regular updates and progress reports. * Regulatory Compliance: Ensure all documentation, including regulatory submissions and patient records, are kept up-to-date and in compliance with ethical and legal standards. * Problem Solving & Innovation: Identify areas for process improvement and implement solutions to drive efficiency and enhance trial operations. What We’re Looking For: * Goal-Driven & Independent: You thrive in an autonomous work environment and take full ownership of your responsibilities. * Innovative & Results-Driven: You are eager to contribute to CVAUSA’s rapid growth and bring fresh, effective solutions to the table. * Detail-Oriented & Highly Organized: You have the ability to manage multiple tasks and deadlines without sacrificing quality. * Strong Communicator: You can effectively communicate with stakeholders at all levels, including sponsors, site staff, and participants. Experience & Qualifications: * Clinical experience in cardiovascular medicine in any licensed role (i.e. RN, technologist, medical assistant, etc.) * Bachelor’s degree in a relevant field (e.g., life sciences, healthcare, or clinical research) * Experience managing clinical trials, leading the enrollment for multiple clinical trials, developing a research program * Strong organizational and time management skills * Clinical research certification (e.g., CCRP) is a plus * Knowledge of GCP, ICH guidelines, and regulatory requirements Powered by JazzHR G6EOMtOOe0

Job Description Job Title: Clinical Research Nurse - Oncology (Downtown) Job Description The Clinical Research Coordinator II RN (CRC-II RN) plays a vital role in the Research Institute, under limited supervision, to plan, coordinate, evaluate, and perform the nursing care of participants, collecting data for assigned research projects. This position requires following study-specific protocol guidelines and maintaining communication with Principal Investigators, Sub-Investigators, Clinical Research Lead, and clinical research support staff. The CRC-II RN advocates for the patient while adhering to the conduct of industry-sponsored and investigator-initiated clinical trials in accordance with trial protocols, FDA regulations, and ICH/GCP guidelines. Responsibilities • Deliver safe care while maintaining the dignity and respect of all participants., • Maintain clinical competencies such as physical assessment, phlebotomy, and IV insertion., • Abide by HIPAA regulations and practice Universal Precautions., • Maintain a clean and prepared clinical space, performing set-up and turnover procedures., • Participate in internal and external training programs to maintain licensure., • Utilize positive interpersonal communication skills with healthcare team members, patients, investigators, and sponsors., • Review elements of the informed consent document in compliance with FDA, state, federal, and institutional regulations., • Manage multiple clinical trial protocols and perform accurate, legible, and timely documentation., • Promote Principal Investigator oversight by advising on deviations, patient status, and trial integrity., • Clinical research experience in oncology and clinical trials., • Skills in chart review and pre-screening patients., • Ability to perform clinical tasks including assisting with minor procedures., • Adaptability to various clinical settings as needed per protocol., • Demonstrated skills in physical assessment, phlebotomy, IV insertion, and administration of investigational drugs., • Associate degree in Nursing., • Minimum of 2 years of clinical research experience., • Current, active State of FL license as a Registered Nurse. The position is based in a hospital setting, requiring adherence to hospital and departmental policies. The role involves working with various healthcare professionals and requires the ability to adapt to different clinical environments. Job Type & Location This is a Permanent position based out of Orlando, FL. Pay and Benefits The pay range for this position is $75000.00 - $98000.00/yr. Benefits from Day One: Medical, Dental, Vision Insurance, Life Insurance, Disability Insurance Paid Time Off from Day One 403-B Retirement Plan 4 Weeks 100% Paid Parental Leave Career Development Whole Person Well-being Resources Mental Health Resources and Support Pet Benefits Workplace Type This is a fully onsite position in Orlando,FL. Application Deadline This position is anticipated to close on Mar 16, 2026. About Actalent Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500. The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing due to a disability, please email for other accommodation options.

A premier healthcare organization in Orlando is looking for a Clinical Research Coordinator to manage and coordinate clinical trials.

Responsibilities * Assist the Clinical Research Coordinator and Investigator in conducting clinical study activities. Ensure adherence to clinical research Good Clinical Practice (GCP) requirements and medical documentation standards. This full-time role involves assisting the Clinical Research Coo