NewPrincipal Investigator (Gastroenterology) Professional Case ManagementPrincipal Investigator (Gastroenterology)Kansas City, KS$156,600–$266,700Risks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes; Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result; Selection of human subjects and patients for research participation is equitable; Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in accordance with, and to the extent required, by company policies and federal regulations; Informed consent of human research subjects will be obtained in advance of research participation and appropriately documented in accordance with, and to the extent required, by company policies and federal regulations; Where appropriate, there is routine monitoring of the data collected to ensure the safety of human research subjects; The privacy of human research subjects is protected and the confidentiality of data is maintained; Appropriate additional safeguards are included in the study to protect the rights and welfare of human research subjects who are likely to be vulnerable to coercion or undue influence (e.g., children, prisoners, individuals with impaired decision-making capacity, or economically or educationally disadvantaged persons). Maintaining adequate, current, and accurate records of research data, outcomes, and reportable new information to permit an ongoing assessment of the risk/benefit ratio of study participation; Reporting promptly any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study; Reporting promptly any significant changes in the risk/benefit of study participation; Ensuring that, in the event a research subject experiences a significant adverse event, every reasonable effort is made to provide the subject with adequate care to correct or alleviate the consequences of the adverse event to the extent possible; Ensuring that human research subjects are kept fully informed of any new information that may affect their willingness to continue to participate in the research study; Ensuring that all listed investigators have the appropriate credentials to conduct the portion of the study in which they are involved and have completed the applicable company required training modules; Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
NewPrincipal Investigator (Psychiatry) Professional Case ManagementPrincipal Investigator (Psychiatry)Kansas City, KS$156,600–$266,700Risks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes; Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result; Selection of human subjects and patients for research participation is equitable; Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in accordance with, and to the extent required, by company policies and federal regulations; Informed consent of human research subjects will be obtained in advance of research participation and appropriately documented in accordance with, and to the extent required, by company policies and federal regulations; Where appropriate, there is routine monitoring of the data collected to ensure the safety of human research subjects; The privacy of human research subjects is protected and the confidentiality of data is maintained; Appropriate additional safeguards are included in the study to protect the rights and welfare of human research subjects who are likely to be vulnerable to coercion or undue influence (e.g., children, prisoners, individuals with impaired decision-making capacity, or economically or educationally disadvantaged persons). Maintaining adequate, current, and accurate records of research data, outcomes, and reportable new information to permit an ongoing assessment of the risk/benefit ratio of study participation; Reporting promptly any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study; Reporting promptly any significant changes in the risk/benefit of study participation; Ensuring that, in the event a research subject experiences a significant adverse event, every reasonable effort is made to provide the subject with adequate care to correct or alleviate the consequences of the adverse event to the extent possible; Ensuring that human research subjects are kept fully informed of any new information that may affect their willingness to continue to participate in the research study; Ensuring that all listed investigators have the appropriate credentials to conduct the portion of the study in which they are involved and have completed the applicable company required training modules; Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
NewPrincipal Investigator (Medical Director) AtriumPrincipal Investigator (Medical Director)Austin, TX$100–$150 / hourThe organization partners with healthcare providers, Research teams, and sponsors to support high-quality clinical studies across multiple therapeutic areas while maintaining a strong commitment to patient safety, operational excellence, and scientific integrity. Responsibilities of the Principal Investigator (Medical Director): Serve as Principal Investigator (Medical Director) or Sub-Investigator for site-based and decentralized/hybrid clinical trials, ensuring patient safety, regulatory compliance, and data integrity.
Principal Investigator (Pediatrics) Professional Case ManagementPrincipal Investigator (Pediatrics)Riverdale, GA$156,600–$266,700Risks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes; Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result; Selection of human subjects and patients for research participation is equitable; Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in accordance with, and to the extent required, by company policies and federal regulations; Informed consent of human research subjects will be obtained in advance of research participation and appropriately documented in accordance with, and to the extent required, by company policies and federal regulations; Where appropriate, there is routine monitoring of the data collected to ensure the safety of human research subjects; The privacy of human research subjects is protected and the confidentiality of data is maintained; Appropriate additional safeguards are included in the study to protect the rights and welfare of human research subjects who are likely to be vulnerable to coercion or undue influence (e.g., children, prisoners, individuals with impaired decision-making capacity, or economically or educationally disadvantaged persons). Maintaining adequate, current, and accurate records of research data, outcomes, and reportable new information to permit an ongoing assessment of the risk/benefit ratio of study participation; Reporting promptly any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study; Reporting promptly any significant changes in the risk/benefit of study participation; Ensuring that, in the event a research subject experiences a significant adverse event, every reasonable effort is made to provide the subject with adequate care to correct or alleviate the consequences of the adverse event to the extent possible; Ensuring that human research subjects are kept fully informed of any new information that may affect their willingness to continue to participate in the research study; Ensuring that all listed investigators have the appropriate credentials to conduct the portion of the study in which they are involved and have completed the applicable company required training modules; Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
Principal Investigator (Neurology) Professional Case ManagementPrincipal Investigator (Neurology)Dallas, TX$156,600–$266,700Risks to research subjects are minimized by using procedures which are consistent with sound research design and which do not unnecessarily expose the subjects to risk; and, whenever appropriate, by using procedures already being performed on the subjects for diagnostic or treatment purposes; Risks to human research subjects are reasonable in relation to the anticipated benefits (if any) to the individual, and the importance of the knowledge that may be expected to result; Selection of human subjects and patients for research participation is equitable; Individuals are adequately informed of the risks and benefits of research participation and the procedures that will be involved in the research, and that informed consent will be obtained from each prospective human research subject, or his/her legally authorized representative, in accordance with, and to the extent required, by company policies and federal regulations; Informed consent of human research subjects will be obtained in advance of research participation and appropriately documented in accordance with, and to the extent required, by company policies and federal regulations; Where appropriate, there is routine monitoring of the data collected to ensure the safety of human research subjects; The privacy of human research subjects is protected and the confidentiality of data is maintained; Appropriate additional safeguards are included in the study to protect the rights and welfare of human research subjects who are likely to be vulnerable to coercion or undue influence (e.g., children, prisoners, individuals with impaired decision-making capacity, or economically or educationally disadvantaged persons). Maintaining adequate, current, and accurate records of research data, outcomes, and reportable new information to permit an ongoing assessment of the risk/benefit ratio of study participation; Reporting promptly any internal or external adverse event that is considered to be unexpected, serious, and possibly or definitely related to the study; Reporting promptly any significant changes in the risk/benefit of study participation; Ensuring that, in the event a research subject experiences a significant adverse event, every reasonable effort is made to provide the subject with adequate care to correct or alleviate the consequences of the adverse event to the extent possible; Ensuring that human research subjects are kept fully informed of any new information that may affect their willingness to continue to participate in the research study; Ensuring that all listed investigators have the appropriate credentials to conduct the portion of the study in which they are involved and have completed the applicable company required training modules; Ensuring that conduct of the research study adheres to Good Clinical Practice guidelines.
Regional Director, Home Care and Research (Nurse Practitioner) Professional Case ManagementRegional Director, Home Care and Research (Nurse Practitioner)Farmington, NM$113,200–$179,100Individual 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. Whether you work in our Home Care, Clinical Research, Impairments, or Catastrophic Care division, you will support our mission to deliver care and other services that enhance the quality of life of our clients.
NewNURSE RESEARCH COORDINATOR Methodist Health SystemNURSE RESEARCH COORDINATORDallas, TXNamed one of the fastest-growing health systems in America by Modern Healthcare , Methodist has a network of 12 hospitals (through ownership and affiliation) with nationally recognized medical services, such as a Level I Trauma Center, multi-organ transplantation, Level III Neonatal Intensive Care, neurosurgery, robotic surgical programs, oncology, gastroenterology, and orthopedics, among others. In addition to customary research coordination activities, the Nurse Research Coordinator, under the direction of the principal investigator, will perform study-related assessments and procedures, such as: physical examinations, transient elastography (TE), electrocardiogram (ECG) infusion therapy, phlebotomy, and administer medications as outlined in the research protocol.
NewClinical Research Coordinator III JouléClinical Research Coordinator IIICarnegie, PAA top-ranked research university is currently searching for a Clinical Research Coordinator III for one of its growing departments to be for all study-related activities including screening & consent and enrollments, data collection/entry, and compliance with the regulatory process. Responsibilities include but are not limited to screening patients to determine eligibility/verification of enrollments, facilitating study activities, coordinating/conducting informed consent discussions, assisting with consent issues, and monitoring patients for complications and outcomes.
Clinical Research Nurse JouléClinical Research NurseRochester, NY$40–$50 / hourManage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study related supplies and equipment, assisting with monitoring visits, attending Investigator Meetings, and assisting with query resolution, as required. Ensure Serious Adverse Events (SAE’s) are reported to Principal Investigator, Sponsor, and IRB (through Regulatory) within 24 hours of site being notified of event, including collecting all required information for initial and follow-up reporting.
Research Associate JouléResearch AssociateRockville, MD$28–$43 / hourStrong computer skills, including proficiency with basic data analysis programs (Microsoft Office, GraphPad Prism, Pristima, etc.) and programming and data analysis (R Studio, Linux, etc.). System One, and its subsidiaries including Joulé, ALTA IT Services, and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
NewResearch Scientist Gables Search GroupResearch ScientistLancaster, SC$75,000–$95,000Performs routine activities such as facilitating site recruitment, site training and study initiation, in-life and close-out activities in order to ensure site activities are in accordance with project objectives. Minimum Education: Masters degree preferably in science, biology, veterinary, or related life science with 4+ years of experience with a producer of nutraceutical or pharmaceutical products.
NewClinical Research Coordinator I (PA/NJ Residents Only) St. Luke's Health Network, Inc.Clinical Research Coordinator I (PA/NJ Residents Only)Bethlehem, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
Clinical Research Coordinator I (PA/NJ residents only) St. Luke's Health Network, Inc.Clinical Research Coordinator I (PA/NJ residents only)Bethlehem, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
Corporate Fraud Investigator Mountain West BankCorporate Fraud InvestigatorSpokane, WAFull timeThis role involves handling cases related to electronic banking fraud (including Zelle), new account abuse, deposit fraud, check forgery, elder abuse, debit and credit card fraud, suspected money laundering, check kiting, identity theft, internal fraud, loan fraud, and other complex schemes. Conduct routine investigations into suspected fraud including identity theft, account abuse, check fraud, elder abuse, debit/credit card fraud, loan fraud, electronic banking fraud (e.g., Zelle), internal fraud, loan fraud, and others.
Research Investigator - Anesthesiology & PeriOp Med - Research University of Texas MD Anderson Cancer CenterResearch Investigator - Anesthesiology & PeriOp Med - ResearchHouston, TX$59,000–$89,000 / yearIn Anesthesiology & PeriOp Medicine - Research, our neuroscience research focuses on the function of voltage- and ligand-gated ion channels and synaptic plasticity in chronic pain, opioid actions, and neurogenic hypertension. Works on general laboratory routine functions including reagent preparation, equipment maintenance, minor repairs on small equipment, inventory bookkeeping and supply ordering.
Research / Sr. Research Investigator, Quantitative Pharmacology Incyte CorpResearch / Sr. Research Investigator, Quantitative PharmacologyWilmington, DEBy accessing this link you can learn about the types of personal data we collect how we use it whether collection and processing is optional sources of the personal data we process how it is shared where it is stored or transferred to how long we keep it and contact information for Incyte Incytes data protection officer and your supervisory authority if applicable. Essential Functions of the Job Key responsibilities Conducts model-based analyses including population pharmacokinetics PK and pharmacokineticspharmacodynamics PKPD and exposure-response modeling under the guidance of senior team members.
Research Support Pharmacist MultiCare Health SystemResearch Support PharmacistTacoma, WAFull timeHome to the MultiCare Regional Cancer Center, a Family Birth Center and specialized neonatal care in partnership with Mary Bridge Children's, our collaborative, mission-driven teams offer a rewarding environment for career growth and professional excellence. Deliver training for pharmacists, technicians, study teams, and patients as needed; serve as a subjectmatter resource for investigational medication use across clinical areas.
Human Subjects Research Compliance Specialist Washington State UniversityHuman Subjects Research Compliance SpecialistPullman, WA$4,508.70–$6,763.06 / monthFull timeThis position has been designated by the department to require a background check because it requires access to children or vulnerable adults as defined by https://apps.leg.wa.gov/rcw/default.aspx?cite=74.34, engages in law enforcement, requires security clearance, interacts with WSU students in a counseling or advising capacity, has access to personal identifying and/or financial information, unsupervised access to university buildings/property, or other business-related need. To request disability accommodation in the application process, contact Human Resource Services: 509-335-4521 (v), Washington State TDD Relay Service: Voice Callers: 1-800-833-6384; TDD Callers: 1-800-833-6388, 509-335-1259(f), or https://hrs@wsu.edu.
Clinical Research Coordinator - Cellular Therapy Providence St. Joseph HealthClinical Research Coordinator - Cellular TherapySeattle, WAFull timeIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington.
Senior Clinical Research Analyst - Tumor Institute Providence St. Joseph HealthSenior Clinical Research Analyst - Tumor InstituteSeattle, WAFull timeIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. This includes preparation of all submissions to the IRB to assure the protection of human subjects in research; FDA-required submissions which may include investigator 1572 forms, investigational new drug applications, device submissions such as Emergency use, HDE, Safety Reports, and other documents that may be required by a regulatory agency or the institution.
Senior Research Investigator, Clinical Pharmacology & Pharmacometrics Bristol-Myers Squibb CoSenior Research Investigator, Clinical Pharmacology & PharmacometricsPrinceton, NJ$146,420–$177,428 / yearThe CP&P team interacts with discovery and translational scientists, project leadership, early development, late development and commercial colleagues to optimize dosing, formulation, delivery and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Senior Research Investigator, Clinical Pharmacology Bristol-Myers Squibb CoSenior Research Investigator, Clinical PharmacologyPrinceton, NJ$146,420–$177,428 / yearThe CP&P team interacts with discovery and translational scientists, project leadership, early development, late development and commercial colleagues to optimize dosing, formulation, delivery and combination strategies to enable faster and more effective drug development informed by core scientific principals and data. Based on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day.
Product Development Research Investigator On-Board CompaniesProduct Development Research InvestigatorMidland, MI$50–$60 / hourToday, On-Board is a thriving privately held family of companies with services including: Consulting, Professional Engineering, Industrial Maintenance and Facility Management, Contracted Manufacturing and Production Services, as well as Temporary Staffing and Recruiting throughout North America. Overview: On-Board PMO is well known for complex program solutions, whether the need is in Production, Operations, Product Processing, Packaging, Warehousing & Logistics, Contract Manufacturing, or Plant Management; On-Board has the infrastructure and experience to provide world-class service.
Research Investigator Sr. University of PennsylvaniaResearch Investigator Sr.Philadelphia, PA$80,891–$94,753 / yearLong-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. As the scope of our 3D printing work expands, the software infrastructure must be actively maintained, improved, documented, and extended to support new phantom designs, new imaging targets, improved realism, and more efficient production workflows.
Clinical Research Coordinator - Tumor Institute Providence St. Joseph HealthClinical Research Coordinator - Tumor InstituteSeattle, WAFull timeTogether, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington. The amounts listed are the base pay range; additional compensation may be available for this role, such as shift differentials, standby/on-call, overtime, premiums, extra shift incentives, or bonus opportunities.
Clinical Research Coordinator - Hematology Providence St. Joseph HealthClinical Research Coordinator - HematologySeattle, WAFull timeIt is comprised of eight hospital campuses (Ballard, Edmonds, Everett, Centralia, Cherry Hill (Seattle), First Hill (Seattle), Issaquah and Olympia); emergency rooms and specialty centers in Redmond (East King County) and the Mill Creek area in Everett; and Providence Swedish Medical Group, a network of 190+ primary care and specialty care locations throughout the Puget Sound. Together, our 120,000 caregivers (all employees) serve in over 50 hospitals, over 1,000 clinics and a full range of health and social services across Alaska, California, Montana, New Mexico, Oregon, Texas and Washington.
Senior Research Investigator University of PennsylvaniaSenior Research InvestigatorPhiladelphia, PA$80,891–$100,000 / yearJob Description: The Senior Research Investigator will build, validate, document, and deploy robust, custom-tailored and user-friendly image analysis pipelines for the analysis of super-resolution microscopy data, including but not limited to single-molecule localization microscopy, single-particle tracking, spatial statistics, and multi-dimensional image analysis. The successful candidate should have a highly analytical mindset and be able to identify analysis needs, design appropriate computational approaches, implement and test software tools, support the biological interpretation of imaging data, and help disseminate methods through publications, grants, and documentation.
Research Investigator, Senior University of PennsylvaniaResearch Investigator, SeniorPA$80,891–$108,725.54 / yearImportantly, this individual should have substantial experience in the growth and manipulation of primary human epithelial cultures and analysis of infection of primary cultures with respiratory pathogens, and have experience with confocal microscopy, cilia beat frequency analysis, and immunologic assays, including flow and flow sorting. Importantly, this individual should have substantial experience in growth and manipulation of primary human epithelial cultures and analysis of infection of primary cultures with respiratory pathogens and have experience with confocal microscopy, cilia beat frequency analysis and immunologic assays including flow and flow sorting.
Research Expert / Research Investigator - Biotransformation (Metabolite Identification), DMPK Incyte CorpResearch Expert / Research Investigator - Biotransformation (Metabolite Identification), DMPKWilmington, DED. in Pharmaceutical Sciences Chemistry Biochemistry or a related discipline with 0-5 years of relevant industry or postdoctoral experience or M.S. with 4-8 years of relevant industry experience or B.S. with 6-10 years of relevant industry experience Experience in biotransformation and metabolite identification in a pharmaceutical or CRO environment Hands-on experience with in vitro metabolism systems e.g. By accessing this link you can learn about the types of personal data we collect how we use it whether collection and processing is optional sources of the personal data we process how it is shared where it is stored or transferred to how long we keep it and contact information for Incyte Incytes data protection officer and your supervisory authority if applicable.
Research Expert / Research Investigator – Biotransformation (Metabolite Identification), DMPK Incyte CorporationResearch Expert / Research Investigator – Biotransformation (Metabolite Identification), DMPKWilmington, DelawareBy accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable). We are seeking an experienced scientist who has the flexibility to provide hands-on (lab-based) support of biotransformation (metabolite identification) activities across a portfolio of small molecule programs.
Sr. Research Investigator University of PennsylvaniaSr. Research InvestigatorPhiladelphia, PA$79,500–$113,000 / yearLong-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 has 12 highly-regarded schools that provide opportunities for undergraduate, graduate and continuing education, all influenced by Penn's distinctive interdisciplinary approach to scholarship and learning.
Clinical Research Physician (Principal Investigator/Sub-Investigator) - Full Time Thermo Fisher Scientific IncClinical Research Physician (Principal Investigator/Sub-Investigator) - Full TimeRichfield, MN$240,000–$315,000 / yearDemonstrated ability to collaborate effectively across a matrixed organization, partnering with clinical operations, recruitment, regulatory, pharmacy, laboratory, and sponsor-facing teams to achieve study objectives. As a business of PPD, we are committed to optimizing each step in the patient journey and delivering best-in-class site performance to bring our customers greater certainty to clinical trial delivery.
Research Investigator, Statistician HealthPartners InstituteResearch Investigator, StatisticianBloomington, MNReporting to the Director of the Research Methodology Group, this role joins a team of seven statisticians with broad methodologic expertise in pragmatic-randomized trials, traditional clinical trials, causal inference, machine learning, predictive analytics, and other topics. In addition to contributing to grant proposals, data analysis for ongoing studies, and dissemination of research findings through presentation and publication, the Research Investigator, Statistician will have the opportunity to develop an independent line of research aligned with organizational mission and their area(s) of expertise.
Research Investigator University of MichiganResearch InvestigatorAnn Arbor, MISupporting ongoing test activities on Hall thrusters, rotating magnetic field thrusters, advanced hollow cathodes, and magnetic nozzles. The Department of Aerospace Engineering in the College of Engineering at the University of Michigan in Ann Arbor is seeking a Research Investigator.
Principal Investigator - Clinical Research QPS Holdings LLCPrincipal Investigator - Clinical ResearchSpringfield, MOQPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. For experienced PIs, QPS provides a platform to focus on quality, mentorship, and meaningful clinical impact, while working closely with sponsors and multidisciplinary teams in a collaborative, well-supported research environment.
Research investigator - Woodland Hills USA Express Legal & Investigative ServiceResearch investigator - Woodland HillsWoodland Hills, CaliforniaUSA Express Legal & Investigative Services is seeking a motivated and detail-oriented Research Investigator to support legal and insurance-related investigations. The ideal candidate is an effective communicator with strong writing skills, an inquisitive mindset, and the ability to work both independently and as part of a team.
RESEARCH INVESTIGATOR University of MichiganRESEARCH INVESTIGATORAnn Arbor, MIIn this leadership position, the candidate will: 1) conduct their own individual research projects; 2) mentor graduate students and research technicians; 3) help in generating data for manuscripts and grant applications; and 4) write and submit their own grant applications as a step to acquire an independent position. The ideal candidate will be supervised by the Principal Investigator in a laboratory that studies the regulation of epithelial differentiation and its interaction with the immune system which are key to the understanding of tissue homeostasis and inflammatory diseases.
Sr Research Engineer-Project Principal Investigator SRI InternationalSr Research Engineer-Project Principal InvestigatorAnn Arbor, Michigan$130,760–$194,505 / yearFull timeQualified candidates are a Principal Investigator or have the experience to develop in the near term into a Principal Investigator, designing new research paths, supervising research staff, and interacting with research sponsors to fund new program directions. Research Engineer to work on-site at our Ann Arbor, MI office, and will participate in multi-disciplinary, collaborative teams and contribute to the development of state-of-the-art remote sensing solutions and surveillance technologies.
Sr Research Engineer Project Principal Investigator SRI InternationalSr Research Engineer Project Principal InvestigatorAnn Arbor, MI$130,760–$194,505 / yearQualified candidates are a Principal Investigator or have the experience to develop in the near term into a Principal Investigator, designing new research paths, supervising research staff, and interacting with research sponsors to fund new program directions. Research Engineer to work on-site at our Ann Arbor, MI office, and will participate in multi-disciplinary, collaborative teams and contribute to the development of state-of-the-art remote sensing solutions and surveillance technologies.
Sr Research Engineer-Project Principal Investigator - RF SRI InternationalSr Research Engineer-Project Principal Investigator - RFAnn Arbor, Michigan$130,760–$194,505 / yearFull timeQualified candidates are a Principal Investigator or have the experience to develop in the near term into a Principal Investigator, designing new research paths, supervising research staff, and interacting with research sponsors to fund new program directions. The salary range is: $130,760-$194,505 Salary ranges will vary and are based on several factors, including geographic location, market competitiveness and equity amongst internal employees in similar roles.
Sr Research Engineer Project Principal Investigator RF SRI InternationalSr Research Engineer Project Principal Investigator RFAnn Arbor, MI$130,760–$194,505 / yearQualified candidates are a Principal Investigator or have the experience to develop in the near term into a Principal Investigator, designing new research paths, supervising research staff, and interacting with research sponsors to fund new program directions. The salary range is: $130,760-$194,505 Salary ranges will vary and are based on several factors, including geographic location, market competitiveness and equity amongst internal employees in similar roles.
Clinical Research Sub-Investigator (PA or NP) Bethany MedicalClinical Research Sub-Investigator (PA or NP)High Point, NCFull timeThe Physician Assistant or Nurse Practitioner will serve as a Sub-Investigator on clinical research studies and will work closely with the Principal Investigator and clinical research team to support protocol execution, participant safety, and accurate clinical documentation. The Triad is home to 85 colleges and universities, including Wake Forest University, High Point University, UNC-Greensboro, NC A&T, Guilford College, Bennett College, and Greensboro College.
Principal Investigator (Assistant, Associate or Full Staff) - Heart, Blood, and Kidney Research Cleveland Clinic FoundationPrincipal Investigator (Assistant, Associate or Full Staff) - Heart, Blood, and Kidney ResearchCleveland, OH$130,000–$300,000 / yearWe are seeking to expand and enhance our research efforts in the areas of cardio-metabolism, vascular biology, atherosclerosis, thrombosis, arrhythmia, renal biology, and heart failure with an open search for NIH funded investigators at the Assistant, Associate, or Full Staff levels who will leverage existing expertise and clinical infrastructure for programmatic efforts. The Department of Heart, Blood, and Kidney Research (formerly Cardiovascular and Metabolic Sciences), chaired by Dr. Stanley Hazen, MD, PhD, in Cleveland Clinic Research, seeks investigators who use multidisciplinary approaches to determine the underlying causes of and develop new treatments for cardiovascular, kidney, and blood diseases.
Breast Medical Oncologist (Research - Clinical Investigator) Orlando HealthBreast Medical Oncologist (Research - Clinical Investigator)Orlando, FloridaFull timeThe incoming physician will play a key role in strengthening the Institute’s breast oncology research platform, contribute to outcomes and translational research initiatives, and work with institutional leadership to identify opportunities within the breast clinical trials portfolio as the program continues to expand. OHCI’s Breast Cancer Center is comprised of a robust, multidisciplinary team of medical, surgical, and radiation oncologists, APPs, and additional cancer care specialists dedicated to providing high-quality, personalized care.
Senior Research Investigator MercorSenior Research InvestigatorNew York, New YorkRemote$70–$100 / hourDesign challenging, real-world physics problems in areas like classical mechanics, electromagnetism, and quantum mechanics. Currently enrolled in or recently completed a PhD program in Physics or a related field.
Principal Investigator – Transportation Research Cervello Global CorporationPrincipal Investigator – Transportation ResearchBozeman, MontanaThe selected PI will lead proof-of-concept development of STRATUM-X Corridor Intelligence—a predictive freight bottleneck forecasting system fusing real-time edge analytics, machine learning, generative AI, and federated learning to deliver actionable corridor-level intelligence for state and local DOTs and private freight operators. CGRC is seeking a Principal Investigator (PI) to lead the research and technical execution of a U.S. Department of Transportation (DOT) SBIR Phase I award under Topic 26-OS2, Freight Corridor Predictive Intelligence.
NewClinical Research Sub-Investigator (NP Or PA) Actalent IncClinical Research Sub-Investigator (NP Or PA)Phoenix, AZ$120,000–$160,000 / yearThis role serves as a Clinical Research Sub-Investigator within a Good Clinical Practice (GCP)-compliant clinical trial environment, providing direct patient care while supporting the safe and accurate conduct of clinical studies. The position requires working closely with patients, clinical staff, and research teams in a structured, protocol-driven setting that emphasizes accuracy, patient safety, and regulatory compliance.
Research Physician - Principal Investigator (Tucson) Arizona Liver HealthResearch Physician - Principal Investigator (Tucson)Tucson, ArizonaThis policy relates to all phases of employment, including, but not limited to, recruiting, employment, placement, promotion, transfer, demotion, reduction of workforce and termination, rates of pay or other forms of compensation, selection for training, the use of all facilities, and participation in all company-sponsored employee activities. This position will be responsible for the clinical oversight/care of research patients and the recruitment, screening, and randomization of patient subjects while ensuring regulatory compliance and data accuracy.
Assistant/Associate Professor - Research and Medical Investigator Louisiana State UniversityAssistant/Associate Professor - Research and Medical InvestigatorBaton Rouge, LAPosition Type: Faculty Department: LSUPBRC ExD - Clinical Science (Juan Lertora (00057945)) Work Location: LSU - Pennington Biomedical Pay Grade: Academic Job Description: Pennington Biomedical Research Center, a world-renowned academic research institute of Louisiana State University, is seeking an Assistant or Associate Professor - Research and Medical Investigator in Clinical Science. Research at Pennington Biomedical is supported broadly by multiple NIH Research Centers, and includes approximately 65 faculty and 20 postdoctoral fellows who comprise a network of 44 laboratories and 13 highly specialized core service facilities.
Cinical Research Sub-Investigator (NP/PA) ObjectiveHealth IncCinical Research Sub-Investigator (NP/PA)Springboro, OHThis is a unique opportunity for an advanced practice provider in Internal Medicine, Family Medicine, or a related field to contribute to innovative clinical research while maintaining a flexible schedule. ObjectiveHealth is seeking a licensed Nurse Practitioner (NP) or Physician Assistant-Certified (PA-C) to serve as a Sub-Investigator at our Dayton, OH research site.