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The CARIO operates at the intersection of research, clinical care, education, and digital innovation, partnering closely with academic leadership, research administration, and IT executives to enable high-impact discovery, efficient research operations, and seamless integration of research into care delivery. Michigan Medicine is seeking a Chief Academic & Research Information Officer (CARIO) to provide executive leadership for the strategy, design, and enablement of informatics, digital, and technology capabilities supporting research, education, and academic operations across the enterprise.

University of Michigan

Chief Academic & Research Information Officer CARIO

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The candidate will work with a clinical research coordinator and the Principal Investigator (PI; Dr. Broome), and get the opportunity to learn about, analyze, and perform statistical analyses on a variety of imaging methods including, but not limited to, REDCap, MiChart (University of Michigan's version of Epic (electronic medical record), and assist with data analysis (using R software, STATA, GraphPad Prism, and/or SAS software), and with drafting/publication of abstracts and manuscripts. The research assistant will be involved in clinical trial recruitment for the PREvention of CardIovascular and DiabEtic kidNey Disease in Type 2 Diabetes (PRECIDENTD) clinical trial (ClinicalTrials.gov link: Study Details | NCT05390892 | PREvention of CardIovascular and DiabEtic kidNey Disease in Type 2 Diabetes | ClinicalTrials.gov).

RESEARCH ASSISTANT I TEMP

Responsibilities will include: synthesis of bioactive molecules and radiochemistry precursors; labeling with carbon-11, fluorine-18, gallium-68, astqtine-211 radionuclides; optimization of reactions, including, purification, characterization and formulation of radiotracers for clinical and pre-clinical research collaborations in neurology and oncology, analyzing outcomes and adverse event information in patient records. Synthesis of bioactive molecules and radiochemistry precursors; labeling with carbon-11, fluorine-18, gallium-68, astatine-211 radionuclides; purification, characterization and formulation of radiotracers for clinical and pre-clinical research collaborations in neurology and oncology, analyzing outcomes and adverse event information in patient records.

RESEARCH FELLOW

We are excited to announce that in partnership with L'Oréal/CeraVe Skincare we are looking for a District Sales Manager to join our team of over 10,000 global field representatives in several regions making over 20 million product details annually for our pharmaceutical and biotech clients. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.

YEAR

IQVIA Holdings Inc

District Sales Manager â Mid-Atlantic Pharmaceutical Sales Leadership - Ped/Derm Experience (OH/PA/KY) â 2478629

Risks 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.

Act for Health

Principal Investigator (Gastroenterology)

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Principal Investigator (Neurology)

Ensure compliance with sponsor and UM policies regarding expenditures and communicate concerns about allowable expenses to PIs; Track cost sharing commitments and monitor expenditure of funds to ensure fulfillment of cost sharing obligations; Track personnel budgeted effort and make salary distribution changes as needed; In partnership with ORSP and Sponsored Programs work to complete various post-award responsibilities including: Processing of award change requests, completing budget reallocations, submitting reports (RPPR's, FSR's Uniform Guidance etc.). Establish sub-accounts for projects when needed; Work extensively with other UM research administrators to establish and monitor sub-account activity; Submit paperwork to Office of Contract Administration to establish subcontracts with external institutions; Assist with submission of yearly non-competing renewals, interim reports, and final reports, ensuring timely submission to ORSP and sponsor.

Research Administrator Senior

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. 8D is a 20-bed, Critical Care unit which provides care for critical and moderate care medical-surgical patients, as well as those patients who are in transition from ICU to general care and rehabilitation floors.

NURSING SUPERVISOR UM Health Adult Hospitals 8D Intermediate CareIntensive Care Unit

Based in Detroit, Henry Ford is one of the nation's most respected academic medical centers and is leading the Future of Health: Detroit, a $3 billion investment anchored by a reimagined Henry Ford academic healthcare campus. We offer a full continuum of services from primary and preventative care to complex and specialty care, health insurance, a full suite of home health offerings, virtual care, pharmacy, eye care and other health care retail.

Henry Ford Hospital

Manager Ophthalmology

Michigan Medicine improves the health of patients, populations and communities through excellence in education, patient care, community service, research and technology development, and through leadership activities in Michigan, nationally and internationally. Or an advanced degree in a health-related areas such as: Health Sciences, Behavioral Sciences, Public Health, Health Care Administration, Clinical Research Administration, Social Work, Psychology, Epidemiology, Foreign MD.

CRC Technician

The Research Assistant will lead participant recruitment and screening, conduct informed consent and study enrollment, and administer virtual social network interviews using Network Canvas software. The ideal candidate is detail-oriented, comfortable engaging diverse participant populations in a virtual research setting, and able to manage multiple study visits and data collection tasks with fidelity to protocol.

HOUR

Ann & Robert H. Lurie Children's Hospital of Chicago

Behavioral Research Assistant-Allergy/Adolescent Medicine

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This role is responsible for gathering, analyzing, and translating client requirements into detailed business and functional requirements, while coordinating cross-functional projects to ensure compliant REMS websites and technology solutions are delivered on time, and in accordance with regulatory requirements. The REMS Business Analyst serves as the critical liaison between business stakeholders, sponsors, and IT teams to ensure the successful delivery of Risk Evaluation and Mitigation Strategy (REMS) programs and supporting REMS solutions.

REMS Operations & Implementation Lead (Remote - US)

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With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. We support the pharmaceutical, biotech, and medical device industries with our proven scientific approach to complex trial data and regulatory submission challenges.

Clinical Jobs in Duncan, MI

Chief Academic & Research Information Officer CARIO University of Michigan

RESEARCH ASSISTANT I TEMP University of Michigan

RESEARCH FELLOW University of Michigan

District Sales Manager â Mid-Atlantic Pharmaceutical Sales Leadership - Ped/Derm Experience (OH/PA/KY) â 2478629 IQVIA Holdings Inc

Principal Investigator (Gastroenterology) Act for Health

Principal Investigator (Neurology) Act for Health

Research Administrator Senior University of Michigan

NURSING SUPERVISOR UM Health Adult Hospitals 8D Intermediate CareIntensive Care Unit University of Michigan

Manager Ophthalmology Henry Ford Hospital

CRC Technician University of Michigan

Behavioral Research Assistant-Allergy/Adolescent Medicine Ann & Robert H. Lurie Children's Hospital of Chicago

REMS Operations & Implementation Lead (Remote - US) MMS

Senior Manager Post-Market Pharmacovigilance (Remote - US) MMS

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