NewManager - Clinical Care Coordination Baptist Health CareManager - Clinical Care CoordinationPensacola, FloridaThe Manager collaborates with physicians, advanced practice providers, operational leaders, population health teams, case management, social workers, quality, and community partners to improve care transitions, reduce avoidable utilization, enhance patient engagement, improve quality outcomes, and support organizational population health initiatives. The Manager provides direct supervision of Clinical Care Coordinators and serves as a clinical and operational leader supporting care coordination activities across the continuum including ambulatory settings, freestanding emergency departments, post-acute providers, community resources, and transitions of care.
Manager, Clinical Operations for Behavioral Health Services - Full Time Hackensack Meridian HealthManager, Clinical Operations for Behavioral Health Services - Full TimeNeptune, New JerseyFull timeResponsibilities: A day in the life of a Manager of Clinical Operations for Behavioral Health Services at Hackensack Meridian Health includes: Supports Clinical Program Managers in ensuring all rules and regulations, including NJ DMHAS/DCF regulations regarding outpatient mental health service and The Joint Commission regulations for Behavioral Health Services. The posted rate of pay in this job posting is a reasonable good faith estimate of the minimum base pay for this role at the time of posting in accordance with the New Jersey Pay Transparency Act and does not reflect the full value of our market-competitive total rewards package.
NewPhysician - Hematology/Oncology - Cone Health Cancer Center at Asheboro Cone HealthPhysician - Hematology/Oncology - Cone Health Cancer Center at AsheboroAsheboro, NCREQUIRED Required: Practitioner must have completed the number of years in a residency program approved by the Accreditation Council for Graduate Medical Education and met all other requirements for eligibility to receive board certification recognized by either the American Board of Medical Specialties or the American Osteopathic Association in the primary medical specialty (or subspecialty) for which the Practitioner is applying for Clinical Privileges. If five (5) or more years have elapsed since the Practitioner completed such residency program, the Practitioner currently must have board-certification recognized by either the American Board of Medical Specialties or the American Osteopathic Association in such specialty (or subspecialty).
NewPhysician - Hematology/Oncology - Cone Health Cancer Center - Annie Penn Cone HealthPhysician - Hematology/Oncology - Cone Health Cancer Center - Annie PennReidsville, NCREQUIRED Required: Practitioner must have completed the number of years in a residency program approved by the Accreditation Council for Graduate Medical Education and met all other requirements for eligibility to receive board certification recognized by either the American Board of Medical Specialties or the American Osteopathic Association in the primary medical specialty (or subspecialty) for which the Practitioner is applying for Clinical Privileges. If five (5) or more years have elapsed since the Practitioner completed such residency program, the Practitioner currently must have board-certification recognized by either the American Board of Medical Specialties or the American Osteopathic Association in such specialty (or subspecialty).
Experienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas Available Thermo Fisher ScientificExperienced Clinical Research Associate (CRA II/Sr CRA) - AR, KS, LA, MO, OK, TX - Multiple Therapeutic Areas AvailableSan Antonio, TexasWhat You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Experienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central US Thermo Fisher ScientificExperienced Clinical Research Associate (Level I/II) - FSP - Multi Therapeutics - Central USDallas, TexasWhat You’ll Do: • Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Experienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas Available Thermo Fisher Scientific IncExperienced Clinical Research Associate (CRA II/Sr CRA) - US Central - Multiple Therapeutic Areas AvailableIN$66,800–$125,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
Experienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas Available Thermo Fisher Scientific IncExperienced Clinical Research Associate (CRA II / SR CRA) - US West- Multiple Therapeutic Areas AvailableSan Diego, CA$84,000–$120,000 / yearWhat You'll Do: Monitors investigator sites with a risk-based monitoring approach: applies root cause analysis (RCA), critical thinking and problem-solving skills to identify site processes failure and corrective/preventive actions to bring the site into compliance and decrease risks. May need to maintain regular contact between monitoring visits with investigative sites to confirm that the protocol is being followed, that previously identified issues are being resolved and that the data is being recorded in a timely manner.
NewContract - Clinical Research Coordinator Science 37Contract - Clinical Research CoordinatorRaleigh, NCMaintains comprehensive knowledge of assigned research protocol to coordinate the comprehensive and compliant execution of assigned protocols in accordance with research governing entity requirements, including but not limited to Sponsor, FDA, and IRB requirements. The Clinical Research Coordinator fulfills the requirements of recruiting, enrolling and conducting follow-up of study participants in clinical trials under the direct supervision of the Principal Investigator (PI) and Project Manager.
Digital Pathology Project Manager Parexel International CorpDigital Pathology Project ManagerNJWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. 3+ years of experience in one or more of the following areas: Project Management, Clinical Trial Operations, Biomarker Operations, Lab Operations, Imaging, and Data Management.