Manager, Clinical Research Data University of RochesterManager, Clinical Research DataWorker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400178 Cancer Center/Clin Trials Ofc Work Shift: UR - Day (United States of America) Range: UR URG 111 Compensation Range: $64,200.00 - $96,200.00 The referenced pay range represents the minimum and maximum compensation for this job. Ability to build collaboration among research team members, laboratory staff, patients and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients) required.
Clinical Research Regulatory Specialist II University of RochesterClinical Research Regulatory Specialist IIAbility to build collaboration among research team members, laboratory staff, patients and families, clinical services (requires tact, sensitivity, clarity, flexibility, empathy for patients) preferred. Develops increased learned skills, flexibility in performing duties, and assumes responsibility for a portfolio of clinical research protocols under the direction of the Principal Investigator (PI) and senior leaders.
Ambulatory Clinical Research Center – RN 2, Outpt University of RochesterAmbulatory Clinical Research Center – RN 2, OutptVisit our website: https://www.urmc.rochester.edu/clinical-translational-science-institute/clinical-research/clinical-research-center/research-nursing.aspx . The Level II Registered Nurse supports peers in the delivery of patient care services and assumes an expanded role which may include charge nurse, preceptor, and committee member responsibilities.
Clinical Research Project Manager B University of PennsylvaniaClinical Research Project Manager BThe FTDC is seeking a Clinical Research Project Manager B (PM-B) who will be responsible for day-to-day management and oversight of the FTDC's federally funded observational research portfolio focused on young onset neurodegenerative diseases including frontotemporal degeneration (FTD), Alzheimer’s disease and related dementias. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Manager, Clinical Research Finance Operations (Office of Clinical Research) University of PennsylvaniaManager, Clinical Research Finance Operations (Office of Clinical Research)Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. Penn Home Ownership Services: Penn offers a forgivable loan for eligible employees interested in buying a home or currently residing in West Philadelphia, which can be used for closing costs or home improvements.
Mgr, Clinical Trials Proj (L) University of RochesterMgr, Clinical Trials Proj (L)Reporting to the Executive Director of Research Operations, this role supervises the Project Management team and oversees project coordination across the Research Base clinical trial portfolio, including study startup, activation, amendments, timeline tracking, accrual/project status monitoring, and closeout for multisite Phase II and III cancer control and cancer care delivery clinical trials. Worker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400119 Surgery-Cancer Control Work Shift: UR - Day (United States of America) Range: UR URG 113 Compensation Range: $77,600.00 - $116,400.00 The referenced pay range represents the minimum and maximum compensation for this job.
Supv, Clinical Research RN Oncology Portercare Adventist Health SystemSupv, Clinical Research RN OncologyIdentified ability to supervise clinical research teams, lead and accept responsibility, exercise authority, and function independently using effective written and verbal communication in English. • Leadership ability, accepts responsibility, exercises authority, and functions independently using effective written and verbal communications.
Per Diem Clinical Research Nurse - Home Visits Science 37Per Diem Clinical Research Nurse - Home Visits$50–$55 / hourWith interest/expertise in Science 37's decentralized model of care delivery, the Mobile Research Nurse will perform delivery of care to participants as well as collaborate with brick and mortar sites, if indicated, for shared clinical trial implementation. Science 37's Nursing Solutions Group brings together expert nurses who share a passion for organizing, planning and implementing mobile clinical nurse services to participants in clinical trials.
Clinical Research Associate/CRA I - FSP Parexel International CorpClinical Research Associate/CRA I - FSPConducts site visits including but not limited to validation visits, initiation visits, monitoring visits, closeout visits and records clear, comprehensive, and accurate visit & non-visit contact reports appropriately in a timely manner. Performs clinical study site management/monitoring activities in compliance with International Conference on Harmonization / Good Clinical Practices, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated Documents.
Clinical Research Specialist II University of RochesterClinical Research Specialist IIWe are seeking a time-as-reported (10 – 15 hours), bilingual (American Sign Language and English) interventionist to work remotely on a randomized clinical trial (RCT), funded by the National Institute of Mental Health (NIMH), focused on a cognitive behavioral intervention to promote treatment-seeking among Deaf adults with mental health disorders. Complete the Deaf CBT-TS training protocol, which includes reviewing the manual and materials for the intervention; attending a workshop covering the theoretical background, intervention principles, procedures, and intervention techniques; completing role-play exercises; and passing an exam with a mock participant.
Manager Clinical Research 62 Moses Cone Medical ServicesManager Clinical ResearchOversees the fiscal operations of the department, including preparing and managing departmental and pharmaceutical studies budgets, ensuring financial accountability and efficient resource allocation to support the successful execution of research projects. The Manager Clinical Research manages team members that work closely with study subjects and other research staff and supervises most steps of the research trial process to collect, compile, document, and analyze clinical research data.
Clinical Trials Proj Mgr II University of RochesterClinical Trials Proj Mgr IIUnder oversight of the Manager of Clinical Trials Projects, the Clinical Trials Project Manager will manage multiple studies’ day-to-day operations, carry out project management for clinical trials run through the URCC NCORP network from protocol development and initiation to study close-out according to regulatory/NCI guidelines, and ensure each study’s integrity. Manages the assigned project during the critical development and launch period and is responsible for working with the URCC NCORP Research Base leadership, Clinical Trial Chairs and Co-Chairs, as well as all cross functional teams to assess the scope of work, deliverables, timelines, milestones and relevant metrics to track progress and ensure all deadlines are met successfully.
NewHead of Biostatistics & Programming (Clinical Research Organization) Zp Group LlcHead of Biostatistics & Programming (Clinical Research Organization)$275,000–$350,000 / yearKeywords: Global Head of Biostatistics, Biostatistics Leadership, CRO, Clinical Research Organization, Executive Leadership, P&L Ownership, Clinical Development, Drug Development, Statistical Strategy, Data Science, Regulatory Compliance, FDA, EMA, PMDA, ICH, Clinical Trials, Business Development, Client Engagement, Global Operations, Life Sciences, Commercial Strategy, Revenue Growth, Global Team Leadership, statistical programming, programming, biostats, biostatistics. This role is ideal for a senior biostatistics leader with strong commercial acumen, global team leadership experience, and a proven track record of business growth within the life sciences industry.
Senior Clinical Research Associate (level dependent on experience) CTISenior Clinical Research Associate (level dependent on experience)Senior Clinical Research Associate ( home based ) (Level dependent on experience) To help support the unique job functions of our CRAs, we have a dedicated training department that offers ongoing therapeutic training sessions from our world-class medical directors, and an experienced and supportive management team that is there to offer continual guidance. For that reason, we treat our team members with the respect they deserve, and our numbers show it: We support career progression – We believe in promoting from within and we have a structured mentoring program and program for recent graduates to provide the support employees need to move forward.
Manager, Clinical Trials Project, CHeT Outcomes University of RochesterManager, Clinical Trials Project, CHeT OutcomesWorker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400980 Neuro-Ctr Health & Tech/Admin Work Shift: UR - Day (United States of America) Range: UR URG 113 Compensation Range: $77,600.00 - $116,400.00 The referenced pay range represents the minimum and maximum compensation for this job. Collaborates with principal investigators and project leadership to design, develop, and implement study protocols, data collection tools, and quality assurance processes.
Clinical Research Project Manager JBL ResourcesClinical Research Project ManagerRemote, NJRemoteJBL Resources is proud to have earned the reputation of being a premier provider of top talent professionals in the fields of engineering, human resources, logistics, operations, and supply chain management. Working here means joining a team of top technical professionals bringing cutting-edge products to the forefrontoffering driven individuals the opportunity to make a meaningful impact every day.
NewClinical Research Project Manager C University of PennsylvaniaClinical Research Project Manager CThe Research Project Manager will take leadership role in developing study documents managing the detailed operations of projects, coordinating activities in single center and multicenter studies (including international sites), quality control, and assisting with grant applications when applicable. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas) Everest Clinical ResearchSenior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas)To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as a Senior Clinical Research Associate (Pain/Oncology/CNS Therapeutic Areas) . Interact with personnel from study Sponsors, investigational sites, vendors, and Everest functional groups to enable quality and on-time execution of clinical trials in compliance with ICH-GCP and relevant local regulations.
NewSupv, Clinical Research Team Member ServicesSupv, Clinical ResearchEnsures teams maintain adequate inventory levels, order approved equipment and supplies, and maintain clinical supply areas. Applicants may review general information about Florida’s background screening requirements at the Florida Care Provider Background Screening Clearinghouse : https://info.flclearinghouse.com/ .
NewClinical Research Associate - Oncology Zp Group LlcClinical Research Associate - OncologyRemote$120,000–$180,000 / yearSEO Keywords: Senior Clinical Research Associate, Oncology CRA, Remote CRA Jobs, Clinical Research Associate Remote, Oncology Clinical Trials, Site Monitoring Visits, GCP Compliance, RECIST Criteria, ECOG Performance Status, CTCAE Grading, Clinical Monitoring, Investigational Product Accountability, CRO Careers. The Senior Clinical Research Associate will oversee monitoring activities across clinical trial sites, ensuring compliance, data integrity, and patient safety.
Senior Clinical Research Associate Zp Group LlcSenior Clinical Research AssociateRemote$155,000–$175,000 / yearKeywords: clinical research, clinical trials, CRA, general medicine, GCP, ICH, regulatory compliance, site monitoring, CTMS, EDC, protocol training, clinical documentation, data review, query resolution, clinical operations, FDA regulations, SOPs, quality oversight, risk-based monitoring, therapeutic areas. The Senior Clinical Research Associate (CRA) will join a remote, contract-based team supporting Phase II and Phase III studies across a variety of general medicine indications within a full-service clinical research environment.
NewCardiology Clinical Research Associate Zp Group LlcCardiology Clinical Research Associate$100,000–$130,000 / yearKeywords: cardiology clinical research associate, CRA, clinical trials, cardiology studies, GCP, FDA regulations, monitoring visits, site management, EDC systems, data integrity, clinical research, pharmaceutical, medical device, cardiovascular trials. Responsibilities of the Cardiology Clinical Research Associate: Monitor cardiology clinical trials at investigative sites to ensure adherence to protocols, GCP guidelines, and regulatory requirements.
NewPrincipal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert) Biotronik SE & Co KGPrincipal Clinical Research Analyst - Class III Medical Devices (EU MDR Clinical Affairs Expert)$165,000–$185,000 / yearWe are seeking a highly experienced Principal Clinical Research Analyst to provide strategic leadership and technical expertise in clinical evaluation, clinical evidence generation, and regulatory compliance for Class III medical devices. The ideal candidate will possess more than 7 years of experience in clinical affairs, clinical research, and regulatory support within the medical device industry, with extensive expertise in the requirements of the European Union Medical Device Regulation (EU MDR 2017/745).
Sr. Contract Clinical Research Associate (Vaccines) Zp Group LlcSr. Contract Clinical Research Associate (Vaccines)Remote$55–$65 / hourKeywords: senior clinical research associate, sr cra, vaccines cra, vaccine clinical trials, infectious disease trials, contract cra, clinical monitoring, ich-gcp, cro, pharmaceutical, biotechnology, remote cra, clinical research associate, cra, vaccines. Contract Clinical Research Associate (Vaccines) role is ideal for an experienced CRA with strong vaccine monitoring experience and the ability to travel across multiple U.S. regions.
Sr. Contract Clinical Research Associate (Oncology) Zp Group LlcSr. Contract Clinical Research Associate (Oncology)Remote$55–$65 / hourKeywords: senior clinical research associate, sr cra, oncology cra, oncology clinical trials, contract cra, clinical monitoring, ich-gcp, cro, pharmaceutical, biotechnology, remote cra, clinical research associate, cra, oncology. Contract Clinical Research Associate (Oncology) role is ideal for an experienced CRA with strong oncology monitoring experience and the ability to travel across multiple U.S. regions.
Sr. Contract Clinical Research Associate (Gen Med) Zp Group LlcSr. Contract Clinical Research Associate (Gen Med)Remote$55–$65 / hourContract Clinical Research Associate (Gen Med) focused on Gen Med will play a critical role in the oversight and execution of Phase I-III clinical studies, with a preference for experience in Cardiology, Endocrinology, and Obesity, while remaining open to other general medicine indications. Keywords: Senior Clinical Research Associate, Contract CRA, General Medicine, Cardiology Clinical Trials, Endocrinology Studies, Obesity Research, Clinical Monitoring, ICH-GCP, FDA Regulations, Remote CRA, Pharmaceutical, Biotechnology.
NewOphthalmology Clinical Research Associate Zp Group LlcOphthalmology Clinical Research Associate$90,000–$140,000 / yearKeywords: ophthalmology, clinical research associate, CRA, clinical trials, GCP, FDA regulations, site monitoring, clinical operations, ophthalmic studies, CTMS, EDC, regulatory compliance, patient enrollment, study coordination. The Ophthalmology Clinical Research Associate role is ideal for a detail-oriented professional with experience supporting ophthalmic clinical trials and ensuring compliance across study activities.
Senior Clinical Research Associate (Oncology) Zp Group LlcSenior Clinical Research Associate (Oncology)RemoteThe Senior Clinical Research Associate will play a critical role in trial execution, site management, and monitoring activities while serving as a key partner to investigative sites and study sponsors. Responsibilities for the Senior Clinical Research Associate: Independently monitor Phase II-III Oncology clinical trials in accordance with ICH-GCP guidelines, study protocols, and SOPs.
Clinical Research Coordinator B/C University of PennsylvaniaClinical Research Coordinator B/CThe CRC-C may act in a lead capacity in coordination with CRU Research Team projects and assist Research Team Managers in overseeing the execution of project timelines as well as completion of study related activities delegated to the research coordinators(A/B) who provide study related support. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Clinical Research Systems & eSource Specialist Cardiovascular Associates of AmericaClinical Research Systems & eSource SpecialistReporting to the Senior Research Systems Administrator, this role partners closely with research coordinators, regulatory staff, investigators, site leadership, and sponsors to ensure research systems effectively support study conduct and participant management. This position supports implementation, configuration, optimization, training, and ongoing support of REALTIME CTMS, eSource, eRegulatory, sponsor systems, and other research technologies.
Clinical Research Center Manager Harvard Medical Faculty PhysiciansClinical Research Center ManagerAs needed, provide age specific care to pediatric and adult patients with or without diabetes mellitus in a collaborative practice, by using competencies in history taking, physical examination, assessment and interpretation of laboratory and related diagnostic tools for purposes of screening and safety assessments of participants participating in clinical research studies. As part of its dedication to excellence, Longwood Specialty Physicians is associated with Harvard Medical Faculty Physicians (HMFP) and Beth Israel Deaconess Medical Center (BIDMC), renowned organizations that offer access to innovative research, advanced education, and a network of 680+ physicians.
Group Product Manager (eSource Clinical Data Management) Act for HealthGroup Product Manager (eSource Clinical Data Management)Individual base pay depends on various factors, in addition to primary work location, complexity and responsibility of role, job duties/requirements, and relevant experience, skills and other market-based factors. The GPM will bridge the gap between technical configuration and clinical execution, ensuring our systems are not only compliant and validated but are also driving the future of decentralized, hybrid, and site-based trials.
Financial Spec I, Clinical Trials University of RochesterFinancial Spec I, Clinical TrialsWorker Subtype: Regular Time Type: Full time Scheduled Weekly Hours: 40 Department: 400990 Clin & Trans Science Institute Work Shift: UR - Day (United States of America) Range: UR URG 108 H Compensation Range: $25.14 - $35.24 Under general supervision, the Financial Spec I, Clinical Trials provides administrative and transactional support for clinical research financial operations within OCR.
Clinical Research Coordinator III - Mayerson Center Cincinnati Children’s HospitalClinical Research Coordinator III - Mayerson CenterAs a hospital-based Child Advocacy Center, it provides comprehensive, multidisciplinary care to more than 2,000 children each year while partnering with medical, social service and community agencies to deliver coordinated, child-focused support JOB RESPONSIBILITIES . Serve as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations.
NewClinical Research Coordinator III Cincinnati Children’s HospitalClinical Research Coordinator IIIServe as CCHMC liaison to internal departments, clinical teams, regulatory agencies, physician's offices, city clinics, government agencies, academic centers, and other organizations. Recruitment/Enrollment/Retention - Determine best method/s to identify potential participants for research protocol (advertisements, chart reviews, monitoring of clinic schedule, etc.) and prepare accordingly.
Clinical Research Coordinator MRINetwork JobsClinical Research CoordinatorClinicalResearch #CRCJobs #ClinicalTrials #HealthcareCareers #DallasJobs #ResearchCoordinator #NowHiring #MedicalResearch #OnsiteJob #TexasCareers. The position involves coordinating study activities, collecting data, ensuring compliance, and collaborating with physicians, sponsors, and research teams to keep studies on track and accurate.
NewClinical Research Associate (Cardiology/Neurology) Zp Group LlcClinical Research Associate (Cardiology/Neurology)$100,000–$135,000 / yearKeywords: Clinical Research Associate, CRA, Cardiology, Neurology, Cardiovascular Clinical Trials, Neuroscience Clinical Trials, GCP, ICH-GCP, FDA Regulations, Site Monitoring, EDC, eTMF, CTMS, Clinical Operations, Pharmaceutical, Biotechnology. The Clinical Research Associate role is ideal for a detail-oriented professional with experience monitoring cardiovascular or neurological studies and ensuring compliance with regulatory and protocol requirements throughout the lifecycle of the clinical trial.
NewClinical Research Associate Zp Group LlcClinical Research AssociateRemote$100,000–$125,000 / yearThe Clinical Research Associate role is ideal for an experienced professional with strong expertise across non-oncology therapeutic areas including Cardiovascular, CNS, Diabetes, and GLP-1 studies. Requirements of the Clinical Research Associate include: 3+ years of CRA experience with strong exposure to Cardiovascular, CNS, Diabetes, and GLP-1 trials.
Associate Director, Clinical Affairs Becton Dickinson Medical DevicesAssociate Director, Clinical AffairsPlan and direct complex activities with large scale or significant business impact with the accountability for successful completion of all deliverables including but not limited to: Oversee the relationship management of physicians/investigators, other medical professionals, Research Organizations (CRO's), hospitals, research institutions and/or vendors. The role leads managers and teams across multiple large‑scale initiatives, partners closely with investigators, hospitals, CROs, and internal stakeholders, and ensures regulatory compliance, data integrity, and study execution from initiation through completion.
Clinical Research Coordinator- Neurology Epilepsy Yale UniversityClinical Research Coordinator- Neurology EpilepsyHealthcare workers (HCW) are defined as university employees working a healthcare setting who have the potential for direct or indirect exposure to patients, human research subjects or infectious materials including body substance, contaminated medical supplies, devices and equipment, surfaces, or air. HCW have specific health requirements that must be met prior to starting work, including MMR vaccine or immunity, varicella (chickenpox) vaccine or immunity, TB screening, COVID vaccine according to University policy, hepatitis B vaccine or immunity, and annual flu vaccination.
Senior Specialist, Clinical Research Becton Dickinson Medical DevicesSenior Specialist, Clinical ResearchFor most roles, we require a minimum of 4 days of in-office presence per week to maintain our culture of excellence and ensure smooth operations, while also recognizing the importance of flexibility and work-life balance. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per year—to look at the impossible and find transformative solutions that turn dreams into possibilities.
Oncology Clinical Research Associate (CRA) Zp Group LlcOncology Clinical Research Associate (CRA)$120,000–$135,000 / yearResponsibilities for the Oncology Clinical Research Associate: Monitor clinical trials to ensure compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Locations for the Clinical Research Associate: Wisconsin, Michigan, Illinois, Indiana, Ohio, Oklahoma, Nebraska, Utah, Colorado, New York and Massachusetts.
Clinical Research Associate II Zp Group LlcClinical Research Associate IIRemote$100,000–$110,000 / yearKeywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development. Piper Companies is seeking a Clinical Research Associate II to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel across the United States.
Senior Clinical Research Associate I Zp Group LlcSenior Clinical Research Associate IRemote$115,000–$125,000 / yearKeywords: clinical research, clinical trials, CRA, GCP, ICH, regulatory compliance, site monitoring, clinical monitoring, CTMS, EDC, cardiovascular studies, CNS trials, diabetes research, GLP-1, site management, FDA regulations, clinical operations, documentation, quality assurance, protocol compliance, investigator sites, patient safety, clinical development. Piper Companies is seeking a Senior Clinical Research Associate I to join a global organization within the clinical research and life sciences industry for a remote permanent role with 60-75% travel to sites in the US.
Clinical Research Associate Oncology Zp Group LlcClinical Research Associate Oncology$100,000–$135,000 / yearThe Clinical Research Associate (Oncology) role is ideal for an experienced professional with strong oncology monitoring expertise who is passionate about ensuring high-quality clinical trial execution and advancing innovative research. Piper Companies is seeking a Clinical Research Associate (Oncology) to support a rapidly growing organization within the clinical research and life sciences industry.
Clinical Research Coordinator III - (Training & Onboarding Spec) Cancer & Blood Diseases Institute Cincinnati Children’s HospitalClinical Research Coordinator III - (Training & Onboarding Spec) Cancer & Blood Diseases InstituteThe role serves as a highly visible representative of the clinical research division and works collaboratively with research staff, faculty, sponsors, contract research organizations (CROs), and institutional partners to foster a supportive, efficient, and compliant research environment. This position oversees protocol training and onboarding activities for Oncology, Hematology, and Bone Marrow Transplantation research personnel while supporting division-wide operational initiatives, process improvement efforts, and special projects.
Assistant Clinical Manager -Infusion Clinic Advocate Health and Hospitals CorporationAssistant Clinical Manager -Infusion ClinicProviding care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
Manager Clinical Operations (RN)- Medical/Surgical 4W Advocate Health and Hospitals CorporationManager Clinical Operations (RN)- Medical/Surgical 4WPhysical Requirements and Working Conditions : Ability to travel locally as well as long distance travel Ability to work within stressful conditions and difficult situations Resilient and flexible in a changing environment May be exposed to hazardous material and life threatening diseases Ability to cooperate and work with others Ability to make sound and timely decisions. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise.
Clinical Research Coordinator A (Department of Neurosurgery) University of PennsylvaniaClinical Research Coordinator A (Department of Neurosurgery)Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. The Neurosurgery Clinical Research Division of the Department of Neurosurgery at the University of Pennsylvania seeks a full time Clinical Research Coordinator- A. This position will assist in the management of multiple clinical research studies and responsibilities in specific research area.
Vice President of Patient Recruitment, Lynd Clinical 25madisonVice President of Patient Recruitment, Lynd ClinicalOur model combines owned site infrastructure with a proprietary AI platform that analyzes longitudinal medical records to identify, screen, and enroll high-quality participants with speed and precision: driving faster enrollment and better trial outcomes for both sponsors and trial participants. The Vice President of Patient Recruitment will build and oversee Lynd's centralized patient recruitment and enrollment function, supporting all current and future research sites across the network.