Collecting information
Organizing data
Under direction of a Research Clinical Trial Operations leader, the Lead Clinical Research Coordinator will independently coordinate and will be accountable for the overall administration and outcome of multiple clinical studies within the Clinical Trials Office, requiring advanced-level knowledge and skills, involving human subjects that are being conducted within the Nicklaus Children's Research Institute.. Oversees study conduct including all support data collection for study start-up activities.. Submits protocol amendments and other documents requiring IRB submission to the Research Regulatory Affairs team and notifies CTMS support staff for protocol digitization.. Compiles accurate CTMS metrics data for updating SAC CTO slides and runs weekly enrollment reports for management review.. Clinical research certification through SOCRA or ACRP (CCRC, CCRP, CRA) required within 1 year in position
They are seeking a Clinical Research Coordinator (CRC) responsible for coordinating and managing clinical trials and research studies in accordance with regulatory requirements, study protocols, and institutional policies.. The CRC will work closely with investigators, sponsors, and study participants to ensure the ethical and accurate collection of data and the integrity of the research process.. Coordinate day-to-day clinical trial activities and ensure compliance with the study protocol, Good Clinical Practice (GCP), and regulatory guidelines.. Knowledge of clinical research regulations and GCP.. Experience with IRB submissions and sponsor communications.
Join a thriving dermatology practice in Aventura, FL with Skin and Cancer Associates!. We're looking for a General Dermatologist with interest in doing Clinical Research to join our friendly, highly trained team dedicated to clinical excellence and an outstanding patient experience.. Practice Autonomy - Build your desired practice mix (General Dermatology, Surgical, and Cosmetics) Compensation & Benefits: Competitive Compensation Structure - Guaranteed first-year salary or Personal Net Collections (the greater of) Dermatologist Salary Range: $400,000-$500,000 Partnership & Shareholder Track - Grow your career with ownership opportunities.. Full-time (4 or more days per week schedules) Relocation Reimbursement Commencement Bonus Paid Malpractice and Tail Coverage Who We're Looking For: Board-Certified or Board-Eligible Dermatologist Interested in learning Clinical Research Passionate about patient care and clinical excellence About SCA: Skin and Cancer Associates (SCA) and the Center for Cosmetic Enhancement (CCE) is one of the premier dermatology groups in the United States.. We are also at the forefront of some of the most advanced dermatology research and clinical trials.
Provides direct patient care on a daily basis and provides all necessary medical record documentation including Medicare/Medicaid and third-party payers' requirements. Follows established departmental policies, procedures, and objectives, continuous quality improvement objectives, and safety, environmental, and/or infection control standards. Participates in utilization review, quality assessment and improvement programs to improve patient care. Collaborates with Radiology, Pathology, Surgery, Medical Oncology, and Nursing in the clinical management of patients. Complies with all applicable JHS policies and procedures, laws and regulations, and accreditation requirements (including HIPPAA and clinical trials protocol).
CRS is Sylvester's centralized clinical trial office, supporting cutting edge Phase 1-3 oncology clinical trials for its catchment area.. Clinical Research Coordinator 1. Clinical Research Coordinator 2. Clinical Research Coordinator 3. Phlebotomist 2 - Various locations throughout South Florida (Plantation, Kendall, Aventura)
NeueHealth delivers clinical care to health consumers through our owned clinics – Centrum Health and Premier Medical – as well as unique partnerships with affiliated providers across the country. The Utilization Management (UM) Prior Authorization (PA) Nurse is a full-time role with NeueHealth, dedicated to promoting quality and cost-effective outcomes for the designated population. Evaluate and process prior authorization requests for medical procedures, medications, and services based on clinical guidelines such as: Medicare criteria, Medicaid/Medi-Cal criteria, InterQual, MCG, or Health Plan specific guidelines. Familiarity with insurance authorization processes, medical billing, and coding (e.g., ICD-10, CPT codes). Working knowledge of MCG, InterQual, and NCQA standards.
Under the direction of the Care Management Leadership team, the Registered Nurse High Risk Patient Care Navigator will provide high level clinical support for identified High Risk patients with complex medical conditions and transition of care by identifying gaps through close monitoring via telephonic outreaches empowering patients with education and management of acute or chronic conditions.. The Registered Nurse High Risk Patient Care Navigator will serve as a resource, mentor and support for the Care Management Coordinators and Regional Managers.. The Registered Nurse High Risk Patient Care Navigator serves as an intermediary between the Interdisciplinary Care Teams and the patient and/or family, fostering a team-based approach ensuring continuity of care.. Ensure care is provided in compliance with Value Based Care guidelines. Tech Savvy: Proficiency with electronic health record (EHR) systems, healthcare analytics tools, and Microsoft Office Suite (Word, Excel, PowerPoint).
destinationone Consulting specializes in recruitment across diverse sectors, including Healthcare, Health Tech, Government, Municipalities, Non-Profits, Legal, Public Accounting, Food and more.. The Quality Assurance Coordinator is responsible for monitoring and evaluating the quality of care provided within the healthcare practice, ensuring that standards are met and continuously improved.. Bachelor's degree in Healthcare Administration, Nursing, or a related field; certification in quality management preferred.. Experience in quality assurance or improvement in a healthcare setting.. Disclaimer: We're proactively building a databank for opportunities in Healthcare, Health Tech, Government, Non-Profits, Legal, and more.
Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.. Obtains and records initial and ongoing patient information throughout the cycle of care, including admissions data, vital signs, height and weight, blood pressure, oxygen saturation, intake and output, calorie counts, and other patient information as outlined by policy.. Serves as Monitor/Telemetry Tech for the unit as needed.. We hold the only Level III NICU in northern Broward County.. - Dr. Thomas Frist, Sr. HCA Healthcare Co-Founder If you are looking for an opportunity that provides satisfaction and personal growth, we encourage you to apply for our Patient Care Technician opening.
We are seeking a compassionate, detail-oriented Registered Nurse (RN) to join our MSU team.. In this role, you will deliver direct patient care, monitor for withdrawal symptoms, administer medications, and collaborate with physicians, behavioral health specialists, and case managers to provide holistic, patient-centered care.. Associate's degree in Nursing (ADN) or Bachelor of Science in Nursing (BSN).. Certification in a nursing specialty (e.g., Critical Care, Psychiatry).. Preferred skills, such as proficiency in EHR systems, will enhance your ability to document care accurately and streamline communication within the healthcare team.
Conducts Phase 1-4 Clinical Trials for patients and captures study-related data for sponsors.. Documents patient/study results using the electronic medical record (EPIC) and completes data requirements for sponsors.. Screens and consents patients for clinical trials using Good Clinical Practice (GCP) guidelines.. Education and Certification Requirements: Accredited Program (Required)Foreign Medical Doctor Degree (FOREIGN MD DEGREE) - Classroom Training (CLASSROOM TRAINING), Registered Nurse Compact License (RN LICENSE COMPACT) - Compact RN Multistate, Registered Nurse License (RN LICENSE) - State of Florida (FL). Proof of Graduation certificate for foreign trained MDs or equivalents clinical programs.
Were looking for a General Dermatologist with interest in Clinical Research to join our friendly, highly trained team dedicated to clinical excellence and an outstanding patient experience.. Practice Autonomy Build your desired practice mix (General Dermatology, Surgical, and Cosmetics).. Dermatologist Salary Range : $400,000-$500,000.. Board-Certified or Board-Eligible Dermatologist. For convenience, we offer telehealth services via the Pocket Patient App. Review our dermatology services for detailed information, including provider and location details.
Join to apply for the Telemedicine Infectious Disease Physician role at NuView Health. NuView Health is a leader in both on-site Intensivist and multi-specialty telemedicine programming.. We are seeking a board-certified Infectious Disease Physician to join our growing telemedicine team.. As a Remote Infectious Disease Telemedicine Doctor, you will provide expert virtual consultations to patients across diverse healthcare settings.. Provide patient audio/ visual telemedicine consultations via an onsite telemedicine cart.
Global Clinix is seeking a dedicated and experienced Principal Investigator (PI) with a background in Internal Medicine, Family Medicine, or any specialty to join our dynamic clinical research team.. The PI will play a pivotal role in ensuring protocol compliance, patient safety, and regulatory adherence while supporting the success and integrity of ongoing and future clinical trials.. Report serious adverse events (SAEs) and safety concerns in a timely and accurate manner to the sponsor and IRB. Preferred experience in clinical trials, either as a Principal Investigator or Sub-Investigator. Strong understanding of Good Clinical Practice (GCP) and applicable FDA regulations
Join to apply for the Regulatory Affairs Manager role at Katalyst CRO. Facilitate and prepare U.S. regulatory Pre-Submission documents for Next Generation Sequencing and/or PCR assays. for Next Generation Sequencing and/or PCR assays. B.Sc. or equivalent in Biology, Chemistry, Bioengineering, or related science with at least 5 years of IVD Regulatory Affairs experience. Knowledge of regulatory strategy creation, design control, cGMP/Quality Systems, and import/export requirements.
Join to apply for the Regulatory Affairs Manager role at BioSpace.. Collaborate with Regulatory Operations to enhance regulatory submission and information management capabilities within the Veeva RIM platform.. Get notified about new Regulatory Affairs Manager jobs in Coral Gables, FL. Senior City Policy and Regulatory Affairs Manager, MiamiCompliance Specialist - Affordable HousingHealthcare Facilities Compliance Manager.. Prevention Of Sexual Abuse / Performance Quality Improvement Compliance Manager
Join to apply for the Regulatory Affairs Manager role at Catalyst Pharmaceuticals, Inc. Organize and track the internal review process of regulatory documents, including reconciliation of review comments, editing, formatting, version control, and finalization within the Veeva RIM Platform.. Collaborate with Regulatory Operations to enhance regulatory submission and information management capabilities within the Veeva RIM platform.. Solid understanding of Good Clinical Practice (GCP) and end-to-end regulatory submissions and archival processes.. Get notified about new Regulatory Affairs Manager jobs in Coral Gables, FL.
We are seeking a Chief Medical Officer (CMO) in Pulmonary Medicine to be our clinical expertise in pulmonary and critical care with administrative responsibilities. The CMO will be responsible for overseeing all clinical, research, and educational activities within the department, ensuring the highest standards of patient care, advancing medical knowledge, and fostering a collaborative environment. Provide strategic leadership and direction for the Pulmonary Medicine department. Promote and facilitate research initiatives and clinical trials in pulmonary medicine. The Chief Medical Officer, Pulmonary Medicine, will report directly to the CEO.
Organize and track the internal review process of regulatory documents, including reconciliation of review comments, editing, formatting, version control, and finalization within the Veeva RIM Platform.. Collaborate with Regulatory Operations to enhance regulatory submission and information management capabilities within the Veeva RIM platform.. Support the implementation of the Veeva RIM platform in collaboration with internal and external stakeholders and vendors.. Solid understanding of Good Clinical Practice (GCP) and end-to-end regulatory submissions and archival processes.. Proficiency in Veeva Regulatory Information Management (RIM) platform–required
Clinical Research Coordinator II. We’re partnering with a leading clinical research network to hire a Clinical Research Coordinator II.. The CRC II will serve as both a hands-on coordinator, ensuring trials are conducted in compliance with protocol guidelines, regulatory standards (GCP/ICH), and internal procedures.. Coordinate all phases of the trial process including site activation, patient recruitment, visit scheduling, regulatory document management, data entry, safety reporting, and close-out activities.. Ensure confidentiality and HIPAA compliance in handling patient and sponsor data.