Healthcare & Pharma Careers

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

The Clinical Research Coodinator I conducts and manages clinical trials in accordance with the study protocol,GCP, and Velocitys SOPs.. Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and Velocitys SOPs. Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development review, scheduling subjects, protocol training, collection of regulatory documents, conducting visits, ensuring data is entered in a timely manner and all queries are resolved, managing, and reporting adverse events, serious adverse events, and deviations, implementing new protocol amendments, providing all close out reports.. Create, collect, and submit regulatory documents to Sponsors and IRBs as required per protocol, GCP/ICH regulations, and IRB requirements.. Perform clinical duties (e.g. drug preparation and administration, fibroscan, phlebotomy, ECG, lab processing) within scope

Facets Analytical & problem solving skill Operating System: Windows Applications: Facets Automation tools: The client’s homegrown tool developed in Informatica.. Testing tools: Oracle SQL for data validation and Facets for claims testing.. Top 3-5 desirable attributes/qualifications: 5 years’ experience with Facets platform, Medical Plan Benefit Configuration, Provider Network & Agreement Configuration, Understanding for Medicare/Medicaid.. Strong communication and interpersonal skills Required levels/ Years of Experience education: Bachelor’s degree or equivalent work experience Note: Hybrid - 2 days per week in office Work hours : 8AM to 5PM – 1 hour break (8 hours a day , 40 hours a week).. The Management, contractors, and staff of VIVA USA shall respect others without regard to race, sex, religion, age, color, creed, national or ethnic origin, physical, mental or sensory disability, marital status, sexual orientation, or status as a Vietnam-era, recently separated veteran, Active war time or campaign badge veteran, Armed forces service medal veteran, or disabled veteran.

Advanced Practice Provider (Nurse Practitioner or Physician Assistant) to apply medical knowledge and experience, under the direction of the principal investigator and/or research nurse manager.. The Stanford Early Drug Development Program comprises of Phase 1 and Precision Oncology clinical trials, offering novel therapies to patients with advanced solid tumor malignancies, supporting care provided by every CCP in the Cancer Center and SHC's growing network.. Specific functions pertaining to the Service, Clinic or Department are established by the PA and his/her supervising physician(s), and approved by the appropriate medical and nursing administrators, the IDPC, the Credentials & Privileges Committee, the Stanford Hospital and Clinics (SHC) Medical Executive Committee and the SHC Board Credentials, Policies and Procedures Committee.. Orders physical therapy, occupational therapy, respiratory therapy, radiology examinations and nursing services.. DEA - Drug Enforcement Administration

Associate degree required (Health Administration, Business, Health Science, Nursing/Patient Care preferred). Certified Clinical Research Coordinator (CCRC) within 1.5 years required. It is the policy of Franciscan Alliance to provide equal employment to its employees and qualified applicants for employment as otherwise required by an applicable local, state or Federal law.. Franciscan Alliance reserves a Right of Conscience objection in the event local, state or Federal ordinances that violate its values and the free exercise of its religious rights.. Franciscan Alliance is committed to equal employment opportunity.

The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents.. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.. In collaboration with the In-house Clinical Research Associate (IHCRA) and Regulatory Start-Up Associate (RSA), prepare site essential documents, and support the ethics and regulatory submission and approval processes as needed.. Preferably experience of working in the research, pharmaceutical industry or a related field per job level as follows: At least 2-3 years of Clinical Research Associate experience in the Clinical industry.. Novotech is a global full-service clinical Contract Research Organization (CRO) and consists of two operating brands, Novotech and PPC. Novotech is a clinical CRO with labs, phase I facilities, and drug development consulting services.

We are thrilled to offer an extraordinary opportunity for a dedicated Clinical Research Nurse to join our dynamic team at Memorial Health University Medical Center, part of HCA Healthcare, the nation's top provider of healthcare services.. Family support initiatives, including fertility assistance and adoption support.. The Clinical Research Nurse Specialist plays a crucial role in coordinating research protocols, serving as the key link between local investigators, clinical staff, and research personnel.. Facilitate patient enrollment in clinical trials through recruitment, screening, and follow-up processes.. We encourage you to apply for this rewarding Clinical Research Nurse position today!

The Clinical Research Associate will support clinical research activities within research sites that are actively participating in clinical trials.. Under the direction of the Clinical Study Manager(s), the Clinical Research Associate (CRA) will assist with study and site start-up activities by working directly with assigned clinical sites and assist with overall study execution.. The CRA may also assist with data management, vendor management and site monitoring as needed.. ; Facilitate timely and accurate communication flow between the clinical study sites, sponsor and applicable vendors; Collaborate with clinical study site and sponsor to troubleshoot and provide appropriate solutions to study-related issues, as appropriate; Assist in patient recruitment activities; Assist with the development of study-related documents as requested; Prepare accurate and timely study reports as requested; Work independently and under general supervision.

As an Associate Director, Global Regulatory Affairs Marketed Products you will define, develop and lead global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple projects.. Lead regulatory reviewer in due diligence for licensing opportunities.. Partner with global market access colleagues to Lead interactions with joint regulatory/health agency/HTA bodies on product specific value evidence topics, as applicable.. Demonstrates acceptable skills with increasing independence in the area of regulatory strategy such as understanding broad concepts within regulatory affairs and implications across the organization and globally; proactively identifies regulatory issues; offers creative solutions and strategies, including risk mitigation strategies.. This position is currently classified as "hybrid" in accordance with Takeda's Hybrid and Remote Work policy.

Through the practice of professional nursing the Oncology Clinical Research Nurse (RN) I prioritizes and advocates for the best interest of the patient enrolled on an oncology clinical trial while maintaining the fidelity of the clinical research protocol and compliance with policies, procedures and regulations.. The oncology clinical research nurse works independently under the general supervision of the Clinical Trials Office Management and Leadership and the Principle Investigator for the specific protocol in order to competently support the safe, high quality and compliant conduct of oncology clinical research and ensure the protection of the patient.. The oncology clinical research nurse I is expected to develop and maintain competencies in clinical research nursing in the first year of the position including but not limited to comprehension and compliance with all NYU PCC Clinical Trials Office policies and procedures, NYU OSR and IRB policies and procedures, familiarity and application of Good Clinical Practice (GCP) guidelines and Federal Regulations that govern the conduct of human subjects research.. The oncology clinical research nurse I demonstrates nursing skills as required under NY state and federal regulations for RN licensure and the ability to navigate patients successfully through the course of trial participation within assigned DMG from pre-screening through coming off protocol.. Is flexible to support clinical care needs as the assigned DMG and day off are based on CTO, PCC clinical care needs.

Through the practice of professional nursing the Oncology Clinical Research Nurse (RN) I prioritizes and advocates for the best interest of the patient enrolled on an oncology clinical trial while maintaining the fidelity of the clinical research protocol and compliance with policies, procedures and regulations.. The oncology clinical research nurse works independently under the general supervision of the Clinical Trials Office Management and Leadership and the Principle Investigator for the specific protocol in order to competently support the safe, high quality and compliant conduct of oncology clinical research and ensure the protection of the patient.. The oncology clinical research nurse I is expected to develop and maintain competencies in clinical research nursing in the first year of the position including but not limited to comprehension and compliance with all NYU PCC Clinical Trials Office policies and procedures, NYU OSR and IRB policies and procedures, familiarity and application of Good Clinical Practice (GCP) guidelines and Federal Regulations that govern the conduct of human subjects research.. The oncology clinical research nurse I demonstrates nursing skills as required under NY state and federal regulations for RN licensure and the ability to navigate patients successfully through the course of trial participation within assigned DMG from pre-screening through coming off protocol.. Is flexible to support clinical care needs as the assigned DMG and day off are based on CTO, PCC clinical care needs.

BlueRock Therapeutics, a wholly-owned and independently operated subsidiary of Bayer AG, is a leading engineered cell therapy company using its unique cell+gene platform to direct cellular differentiation and genetically engineer cells to create a new generation of cellular medicines that address large patient populations suffering from neurological, cardiovascular, and immunology diseases.. Experience in neurology, ophthalmology and/or cardiovascular therapeutic areas and knowledge of global regulations for the development of cell therapy products is desired.. Represent regulatory CMC on and/or lead matrix teams for cell and gene therapy pipeline products.. The ideal candidate should have a strong background in Regulatory Affairs CMC in a global pharmaceutical and/or biotechnology company with expertise in biologics, deep experience in product development and understanding of US, international regulations, and ICH guidelines related to biologics and cell therapy development.. At least 8-10 years in Regulatory Affairs, CMC, and relevant years in a global pharmaceutical and/or biotechnology company with expertise in biologicals and/or cell and gene therapy products (preferred).

The Nurse Director of Quality Assurance will have a unique opportunity to make significant impacts on the quality of care and patient safety at an amazing hospital in the heart of Illinois.. The RN Director of Clinical Quality and Patient Safety will report directly to the Chief Executive Officer, ensuring that Clinical Performance and Risk Management are central to the hospital’s strategic goals and operations.. The Director will work closely with the Chief Nursing Officer and the Chief Medical Officer to align patient safety and performance improvement initiatives with clinical priorities.. The Nurse Director of Clinical Quality and Risk will enjoy the heart of Illinois, a welcoming community that offers a high quality of life, a low cost of living, and easy access to nearby metropolitan areas.. This hospital recognizes the exceptional value that a talented Nurse Director of Clinical Assurance brings to its healthcare organization.

Bachelor’s Degree in Health Information Management or Health Informatics OR. B.S. in informatics, computer science, statistics, biomedical engineering artificial intelligence AND certification in Health Informatics.. Minimum 2 years’ experience in clinical research or clinical trials. Experience with clinical operations, Health Information Management, or care management. While there isn’t a fixed requirement for weekly onsite days, candidates should ideally be available to come onsite one day a week, if needed.

Under the supervision of the Chief Medical Officer/Patient Safety Officer, the Director of Patient Safety and Quality provides leadership and oversight for developing, managing, evaluating, and enhancing programs of Patient Safety, Quality Performance Improvement, Infection Prevention, and Regulatory Compliance at Sibley Memorial Hospital, Renaissance (skilled nursing facility), Grand Oaks (assisted-living facility), and the outpatient practices that reside in the Sibley Physician Group.. Works closely with Vice Presidents, Directors, Managers, and leaders of the Medical Staff to make Quality Performance Improvement, Infection Prevention, Patient Safety, Regulatory Compliance, and Joint Commission on Accreditation Survey readiness a collaborative effort.. Works to ensure Sibley Memorial Hospital, Renaissance (skilled nursing facility), and Grand Oaks (assisted-living facility) meet all regulatory requirements for Quality/Performance Improvement and ORYX /Core Measure data submission to the Centers for Medicare and Medicaid (CMS) and Joint Commission.. A minimum of ten (10) years acute hospital experience or the equivalent combination of education and experience working in Patient Safety, Quality Improvement, Infection Prevention, and Regulatory Compliance.. CPHQ, HACP, CIC or CHCQM Certification

They are hiring a Medical Billing/AR Representative to support the full accounts receivable cycle.. The Medical Billing/AR Representative will be responsible for the overall day to day functions of the AR process including cash management, collections, insurance claims, and disputes.. Work with insurance companies to file appeals to guarantee max reimbursement.. Assist team in performing month-end close, general ledger reconciliation, and general bookkeeping duties.. 2+ years of experience in full cycle accounts receivable and insurance collections.