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Senior Clinical Care Navigator, Cardiology

Carrum Health

Carrum Health is a healthcare company that partners with employers to provide employees access to high-quality medical care through a network of top providers. Carrum Health aims t

Clinical Research4 hours ago

Full Time Remote Senior

Role Description At Carrum, we live and breathe the mission of transforming the healthcare system to create an unmatched experience for patients. The heart of Carrum Health is a seamless and highly personalized patient experience, enabled by expert care coordination and navigation. As a senior member of the Care Team, the Senior Clinical Care Navigator serves as the lead architect for the most complex patient journeys and multi-system coordination needs. - Manage complex cardiology caseloads, guiding patients from diagnosis through recovery. - Represent the Cardiology Service Line, presenting critical data to leadership and cross-functional partners. - Take ownership of the clinical and operational success of your specific service line. - Use technical writing skills to transform complex workflows into clear, scalable Standard Operating Procedures (SOPs). - Influence care models, setting the gold standard for navigation workflows. - Act as the bridge between COE clinical experts and clinical operations teams. - Partner with cross-functional teams to support internal tools and processes. Qualifications - Registered Nurse with a BSN and 8+ years of progressive experience in cardiology. - Technical savvy to collect, report, and present program metrics. - Ability to work seamlessly in interdisciplinary environments. - Proven ability to manage complex workflows and high-impact responsibilities. - Consistent track record of reliability, growth, and increasing scope of responsibility. - Commitment to providing the highest level of service through empathy, professionalism, and integrity. - Ability to handle confidential information and adhere to HIPAA requirements. - Comfortable interacting through various tech platforms and learning new software quickly. Requirements - Bachelor of Science in Nursing (BSN) from an accredited School of Nursing is required. - Minimum of 8+ years of progressive clinical experience in Cardiology is preferred. - Current and unrestricted Registered Nurse licensure. - Nice to have: Spanish Speaking preferred. - Nice to have: Board certification in Cardiac-Vascular Nursing (RN-BC) or as a Care Coordination and Transition Management (CCCTM) professional is highly recommended. Benefits - Stock option plan. - Flexible schedules and remote work. - Self-managed vacation days, within reason. - Paid parental leave. - Health, vision, and dental insurance. - 401K retirement plan.

View details: Senior Clinical Care Navigator, Cardiology

United States

$85K - $95K / year

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Senior Clinical Trial Manager

Generate Biomedicines

Pioneering generative biology to create breakthrough therapeutics.

Clinical Research5 hours ago

Full Time Remote SeniorTeam 201-500Since 2020H1B Sponsor

Company Site LinkedIn

• Independently manages the operational aspects of Generate Biomedicines’ clinical trials, including vendors such as CROs, central labs, biomarker and specialty laboratories, and clinical trial sites, specifically late stage needs in Asthma/COPD. • Leads cross-functional internal study team meetings and meeting deliverables. • Identification, qualification, and selection of clinical trial sites and investigators alongside CRO including management of key relationships. • Leads day-to-day supervision of clinical trial execution, with a focus on site start up, patient enrollment, monitoring, compliance, and data flow metrics from the clinical sites, CROs and central labs. • Facilitates investigator meetings, kick-off meetings, monitoring training, and various CRO (or other vendor) meetings. • Development and review of specific study documents e.g. informed consent forms, study guidelines, operations manuals, training materials. • Participation in the development of clinical trial protocols, amendments, CRFs, IRB/Ethics applications, and recruitment materials. • Management of clinical study budgets and execution timelines. • Ensures adherence to study timelines and project and program goals. • Attends and leads monitoring oversight visits and effective collaboration with CRO, Investigators, and site staff on any outcomes/findings. • Reviews study reports and metrics to ensure timely collection of clinical data, samples, and lab results. • Collaboration on SOP development and promotion of standardized clinical business tools. • Development of action plans to address protocol compliance, safety, data and administrative issues with investigational sites and CROs. • Maintenance and oversight of Trial Master File for assigned studies. • Collaborate with QA and cross functional teams to ensure inspection readiness activities for assigned clinical trials, ensuring TMF completeness, audit preparedness, and compliance with GCP, SOPs, and applicable regulatory requirements. • Participation in the preparation of presentations of trial data for internal and external parties (management review, scientific meetings, and advisory boards). • Trains and mentors junior staff.

Google Cloud Platform

View details: Senior Clinical Trial Manager

Massachusetts

$140K - $196K / year

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Feasibility Manager – Post Award

Precision For Medicine

Clinical Research8 hours ago

Full Time Remote LeadTeam 1,001-5,000H1B No Sponsor

Company Site LinkedIn

• Leading pre-award feasibility projects • Provide detailed pre-award support to operational strategy and business development teams • Provide feasibility analysis and input for pre-award RFPs • Provide enrollment modelling(s) for agreed study strategy(ies) • Undertake feasibility site outreach for pre award opportunities • Support and/or attend BDM and client calls • Apply process, templates and delivery standards for feasibility pre-award • Leading post-award feasibility projects • Provide guidance for post-award, rescue and standalone feasibility in alignment with study and client requirements • Manage feasibility project team in all aspects pertaining to the conduct of the feasibility • Present feasibility strategy at KOM and provide regular updates to sponsor • Conduct the analysis of the collected site data to provide accurate site identification, enrollment modeling and study strategy (ies) • Support Business Development in client meetings and bid defense presentation

View details: Feasibility Manager – Post Award

United States

$100.6K - $151K / year

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Feasibility Manager – Post Award

Precision Medicine Group

Moving Science Closer to Health

Clinical Research8 hours ago

Full Time Remote LeadTeam 1,001-5,000Since 2012H1B Sponsor

Company Site LinkedIn

• Feasibility Manager is responsible for the management and delivery of pre-award, post-award, rescue, and stand-alone-feasibility projects • Lead pre-award feasibility projects and support business development and operational strategy teams by conducting detailed feasibility analysis and presenting at internal and client meetings • Lead feasibility projects for newly awarded and/or ongoing clinical trials and support start-up and clinical teams with site identification, study strategy(ies) and enrollment modeling • Conduct feasibility analysis and input for pre-award RFPs, including: competitive analysis, historical recruitment analysis, standards of care, drug analysis, epidemiology analysis, site and country analysis • Provide enrollment modelling(s) for agreed study strategy(ies) • Participate in growth of the Feasibility Department and Precision for Medicine

View details: Feasibility Manager – Post Award

United States

$100.6K - $151K / year

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Coordinator Clinical Programs

UF Health

UF Health is the University of Florida’s academic health system delivering “World-class care, built for you,” by combining high-quality patient care, inno

Clinical Research10 hours ago

Full Time Remote Mid Level

Company Site

Role Description Ensures coordination and continuity of patient care for transplant patients in order to maintain organized and efficient support to staff and other health care professionals. Responsible for: - Identifying the patient's alterations in health - Assessing the patient's response to treatment protocols - Communicating appropriate data to physician staff - Implementing nursing interventions based upon established treatment protocols - Anticipating potential outcomes for patients at risk for complications Must demonstrate ability to assess data reflective of the patient's status and interpret the appropriate information needed to identify each patient's requirements relative to age-specific needs and organ(s) transplanted and provide care according to protocols and with practice of nursing. Qualifications - Graduate of an accredited four (4) year baccalaureate program in nursing; in lieu of a BSN, extensive and directly clinically-related experience is required (greater than 10 years directly relatable experience in the solid organ body system) - Master's degree in nursing or master's degree 'eligible' (i.e. completion of academic coursework) or related health care field preferred - Currently licensed as a registered nurse (RN) or Advanced/Registered Nurse Practitioner (ARNP) in Florida - Minimum of 3 years experience in nursing with at least 2 years experience in critical care or transplantation - Knowledgeable in transplant immunology, technical aspects of surgery, interpretation of diagnostic and laboratory data, and clinical management of patients - If experienced in all areas listed, will consider enrollees in baccalaureate program Requirements - Motor Vehicle Operator Designation: Employees in this position will not operate vehicles for an assigned business purpose

View details: Coordinator Clinical Programs

United States

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Clinical Research Associate I

Children’s Minnesota

Children’s Minnesota is one of the largest pediatric health systems in the United States and the only health system in Minnesota to provide care exclusively to children, from before birth through young adulthood. An independent and not-for-profit system since 1924, Children’s Minnesota is one system serving kids throughout the Upper Midwest at two free-standing hospitals, nine primary care clinics, multiple specialty clinics and seven rehabilitation sites. As The Kids Experts™ in our region, Children’s Minnesota is regularly ranked by U.S. News & World Report as a top children’s hospital. Children’s Minnesota is proud to be recognized by Modern Healthcare as one of 2023’s Top Diversity Leaders. The national honor recognizes the top diverse healthcare executives and organizations influencing public policy, care delivery, and promoting diversity, equity and inclusion in their organizations and the industry.

Clinical Research10 hours ago

Full Time Remote Mid LevelTeam 5,001-10,000

Role Description The primary responsibility of the Clinical Research Associate I (CRA I) is support of the research team in the conduct of department research projects. - Perform study startup, implementation, and closeout activities - Assist research team with coordination and entry of research data - Assist with regulatory submissions to the Institutional Review Board, and maintain compliance with all federal and local agencies in accordance with Good Clinical Practice guidelines - Interact with patients and families for securing informed consent, scheduling research visits, and collection of data - Maintain documentation for regulatory binder, adverse event reporting, and communications between sponsors and sites - Other special skills specific to assigned research area may include phlebotomy, sample collection, processing or shipping, ECGs, chart abstraction or other duties as assigned - Manage personal career development and administrative tasks Qualifications - Baccalaureate degree or at least 4 years relevant clinical research, professional experience - High attention to detail with strong written and oral communication skills - Strong computer skills beyond basic familiarity with the most common hardware and software systems - Ability to assist staff working on multiple projects - Experience working with pediatric populations (preferred) Requirements - Promotion to next higher level, typically CRA II, is determined by the Clinical Research Program Manager through performance reviews that take into account both experience carrying out the department's job-related duties/tasks, as well as a demonstrated commitment to professionalism in carrying out those tasks in line with Children's values and organizational policies and procedures. Benefits - Medical, dental, vision, retirement, and other fringe benefits - Positions that require night, weekend or on-call work may be eligible for shift differentials or premium pay

View details: Clinical Research Associate I

United States

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Biostatistician

HEALTH CHOICE NETWORK

Clinical Research11 hours ago

Full Time Remote Mid Level

Role Description The Biostatistician provides statistical leadership and advanced analytic support for community‑engaged research, clinical trials, program evaluations, and quality‑improvement initiatives. This role ensures methodological rigor; oversees data cleaning, merging, and preparation; performs complex statistical analyses; and collaborates with multidisciplinary teams across HCN and partner institutions to generate valid, actionable insights that advance health equity. Key Responsibilities - Statistical Design & Methodology - Develop statistical analysis plans for observational studies, RCTs, quasi‑experimental designs, and community health evaluations. - Conduct power and sample‑size calculations. - Advise investigators on appropriate statistical methods and study designs. - Guide selection of measures, variables, and coding structures. - Data Management & Quality Assurance - Oversee data extraction, cleaning, validation, and merging/linkage from EHR systems, REDCap datasets, and multi‑site data sources. - Build reproducible data pipelines (R, SAS, Stata, SQL). - Convert raw datasets into analysis‑ready formats, consistent with workflows. - Ensure compliance with HIPAA, DUAs, IRB requirements, and internal research SOPs. - Statistical Analysis & Interpretation - Conduct descriptive, inferential, and multivariable modeling (e.g., LMM, GEE, logistic/Poisson regression, survival analysis). - Perform longitudinal, clustered, and multi‑level modeling used in community health research. - Produce tables, figures, and visualizations for internal and external dissemination. - Collaborate with investigators to interpret and contextualize findings. - Research & Grant Support - Contribute to research protocols, IRB submissions, and methodological sections of grant proposals. - Provide biostatistical expertise during project planning, execution, and reporting phases. - Support multi‑site research implementation activities. - Submit and lead grant proposals. - Reporting, Publication & Dissemination - Prepare analytic reports for leadership, funders, and research partners. - Contribute to and lead peer‑reviewed manuscripts, abstracts, and conference presentations. - Translate quantitative findings into clear, actionable insights for diverse audiences. - Collaboration & Stakeholder Engagement - Work closely with researchers, clinicians, data analysts, technical teams, and community health centers. - Participate in and lead research meetings. - Provide statistical consultation and capacity‑building across the research network. Qualifications - Doctoral degree in Biostatistics, Statistics, Epidemiology, or related quantitative field. - Demonstrated expertise in statistical programming (R, SAS, Stata, or Python). - Experience with large health datasets, longitudinal data, and applied analysis in clinical or public health settings. - Strong understanding of epidemiologic methods, statistical modeling, and research design. - Experience working in multi‑site or community‑based research environments. Preferred Qualifications - Experience with EHR‑derived data and community health center environments. - Familiarity with REDCap, SQL, and large‑scale data infrastructure. - Experience contributing to federally funded research (NIH, CDC, HRSA). - Experience working on RCTs or complex multi‑level studies, as seen in NCPCR/CEAL protocols. - Geographic Information Systems (GIS) experience is a plus.

View details: Biostatistician

United States

$90K - $100K / year

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Clinical Scientist Associate Director, Cardiovascular

Amgen

Founded in 1980, Amgen (short for Applied Molecular Genetics) is a biotechnology firm focused on developing human therapeutics. As an employer, Amgen has been d

Clinical Research1 day ago

Full Time Remote Senior

Company Site

• Supports the design, execution, and oversight of cardiovascular trials and other late-phase global clinical studies. • Contributes to protocol development, study execution, medical monitoring support, and clinical data review, ensuring delivery of high-quality, decision-ready clinical data for regulatory submissions and scientific dissemination. • Support the design, start-up, and execution of global cardiovascular trials, ensuring adherence to protocol, regulatory requirements, and data integrity standards. • Contribute to development of clinical protocols, statistical analysis plans, investigator brochures, and regulatory documents, with particular focus on cardiovascular endpoints and safety outcomes. • Collaborates with cross-functional teams to support endpoint strategy, event adjudication processes, and cardiovascular safety monitoring. • Participates in development and oversight of endpoint adjudication charters, safety monitoring plans, and Data Monitoring Committee (DMC) interactions. • Provides clinical input into data management plans, CRF design, and clinical data review, with focus on cardiovascular outcomes endpoints (e.g. MACE, hospitalization events, mortality) and/or cardiac imaging endpoints. • Conducts ongoing clinical data review and signal detection, supporting identification and resolution of safety and data quality issues across global trial sites. • Supports preparation and interpretation of interim analyses, database lock activities, and top-line data readouts. • Assists Development Lead and Clinical Scientist Director with medical monitoring activities and oversight of CROs, vendors, and adjudication committees. • Collaborates with clinical operations, biostatistics, safety, regulatory, and medical affairs teams to ensure successful delivery of cardiovascular outcomes and/or cardiac imaging studies. • Contributes to clinical study reports, regulatory submissions, scientific publications, and presentations for internal and external stakeholders. • Identifies operational or scientific risks and proactively implement mitigation strategies across cross-functional teams.

View details: Clinical Scientist Associate Director, Cardiovascular

United States

$169.8K - $229.7K / year

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Senior Clinical Trial Management

ICON plc

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

Clinical Research1 day ago

Full Time Remote SeniorTeam 10,001+Since 1990H1B No Sponsor

Company Site LinkedIn

Role Description The Senior LOM role is a site aligned E2E partner to streamline communication across cross functional stakeholders throughout trial lifecycles. - Serves as the primary point of communication for sites, facilitating internal client teaming to drive issue resolution. - Intimately understands site operational model and owns relationships with critical site stakeholders to provide a voice for the site to the client's teams. - Contribute to quality Site Selection through participation in site feasibility ensuring consistent conduct of site qualification visits and appropriate follow-up of site qualification visit report and country feasibility report. - Ensures local/country team is meeting recruitment targets with high quality data on time and within study budget by providing input to study level documents and leading/coordinating local team activities in compliance with SOPs, other procedural documents and applicable regulations. - Act as primary company contact for assigned trial sites, engaging with Investigator and Site Staff throughout the life of the trial. - Focuses on investigator engagement through timely follow up with sites. - Drive study compliance by maintaining and updating trial management systems, using study tools and management reports available to analyze trial progress. - Contribute to site level recruitment strategy and contingency planning and implementation in partnership with other functional areas to achieve clinical research target. - Delivers competent vendor management at the country level to support the study. - Ensures high standards for study monitoring by conducting quality local trial team meetings and facilitating SM training, when needed. - Contributes to patient understanding of protocol and patient safety by preparing country specific informed consent in accordance with procedural document/templates. - Ensures trial subject safety in that all AEs/SAEs/PQCs are reported within the required reporting timelines and documented, as appropriate. - Ensures Inspection readiness by maintaining complete, accurate and timely data and essential documents in systems utilized for trial management. - Accountable for ensuring quality data (accurate, valid and complete) is provided by the site and queries are resolved within expected timelines. - Keeps oneself inspection ready and knowledgeable for current work by complying with relevant training requirements. - With focus on quality and compliance, will work closely with SM to ensure CAPA is implemented for audits/inspections or any quality related visits. - Ensure accurate finance reporting and trial delivered within budget by adhering to finance reporting deliverables and timelines. - Keeps the trial in compliance with local regulatory requirements by organizing and ensuring IEC/HA approvals in cooperation with the local Start Up team. - May contribute as a trainer of systems/processes or provide input to functional area in process initiatives, if applicable. - Full utilization by timely and accurate time reporting. - Experience in management and startup of complex Early Phase trials projection with internal matrix clinical teams and sites, as applicable. - Autonomy with execution of local trial management services. - Depth of knowledge with local trial management services. - Process leadership. Qualifications - BA/BS degree. - Degree in a health or science related field. - 3 - 5+ years of trial end to end management experience. - Start-up & Database Locks/Cleaning experience preferred. - Solid Tumor Oncology experience required. - Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures. - Strong IT skills in appropriate software and company systems. - Proficient in speaking and writing the country language and English. - Good written and oral communication skills as appropriate. Requirements - To qualify, applicants must be legally authorized to work in the United States and should not require, now or in the future, sponsorship for employment visa status. - Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Benefits - Competitive base salary and performance related incentives. - Health and wellbeing programmes including medical, dental, and vision coverage where applicable. - Retirement and pension plans. - Life assurance and disability coverage. - Employee assistance programmes and wellbeing resources. - Learning and development opportunities through structured training and career pathways. - Benefits may vary depending on role and location. Company Description ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

View details: Senior Clinical Trial Management

United States

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Clinical Licensing Specialist

Geode Health

Providing mental health services, in-person or virtual visits within a few days. Book on-line or call 888-902-1704.

Clinical Research1 day ago

Full Time Remote Mid LevelTeam 51-200H1B No Sponsor

Company Site LinkedIn

Role Description The Clinical Licensing Specialist (Program Specialist) supports regulatory and credentialing operations by coordinating provider licensure tracking, verification, and renewal processes. This role ensures providers maintain appropriate licensure throughout the hiring process and active employment and supports regulatory documentation requirements related to collaboration agreements and provider licensure compliance. This role is responsible for managing and coordinating the collaboration agreement process across all states, ensuring alignment with varying state-specific regulatory requirements and maintaining accurate, compliant documentation. Estimated Pay Range: $25 - 28/hour Key Responsibilities - Track provider licensure status and renewal timelines to ensure regulatory compliance - Conduct pre-hire licensure verification to confirm provider eligibility prior to onboarding - Support provider licensure progression for provisionally licensed providers during the hiring process - Coordinate licensure renewal reminders and follow-up with providers regarding renewal documentation - Maintain accurate licensure records and documentation within credentialing and compliance systems - Manage and coordinate collaboration agreement processes across all states, including tracking requirements, renewals, and documentation to ensure ongoing compliance with state regulations - Coordinate annual collaboration agreement renewals for Nurse Practitioners and Physician Assistants in accordance with state regulatory requirements - Submit and track collaboration agreements and regulatory documentation as required - Support cross-functional coordination with Compliance, Credentialing, and Operations teams - Assist with compliance documentation, audits, and regulatory tracking activities - Perform other job-related duties consistent with the scope and responsibilities of the role, as assigned Role Scope / Authority - Performs defined compliance and credentialing coordination activities within established policies, procedures, and regulatory requirements. - Exercises judgment within established workflows to ensure provider licensure documentation and renewal timelines are maintained. - Coordinates and manages the multi-state collaboration agreement process, ensuring consistency, completeness, and compliance across jurisdictions. - This role does not have authority for hiring, discipline, or performance management and operates as an individual contributor supporting credentialing and compliance processes. Professional Expectations for This Role - Accountability: Owns assigned responsibilities and follows through on compliance-related processes and documentation. - Integrity: Applies regulatory and organizational policies consistently and maintains accurate documentation. - One Team: Supports collaboration across compliance, credentialing, and operational teams. - Balance: Promotes efficient workflows and escalates process or compliance risks appropriately. - Continuous Improvement: Identifies opportunities to improve compliance tracking and documentation processes. - Servant Leadership: Supports operational and regulatory processes while working within defined scope and authority. Qualifications - Strong organizational and documentation management skills - Ability to manage multiple regulatory timelines and deadlines across states - High attention to detail and accuracy - Effective communication and follow-up with providers and internal teams - Ability to maintain confidentiality of provider and organizational information Requirements - Bachelor’s degree preferred - 2–4 years of experience in healthcare credentialing, provider enrollment, compliance coordination, or licensure administration preferred - Experience working with credentialing systems, licensing boards, or regulatory documentation preferred - Experience supporting multi-state licensure and collaboration agreement processes strongly preferred Benefits - Competitive compensation - Flexible schedule - In-person and virtual patient visits - Comprehensive admin support (front office, accounting, finance, payroll, HR, etc) - Professional development opportunities - Clinical community, support, and leadership - Medical, dental and vision benefits - Life insurance - Short and long-term disability - Paid vacation and holidays - Matching 401k plan - State of the art technology

View details: Clinical Licensing Specialist

United States

$25 - $28 / hour

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