Institutional Research Director jobs in Bloomington, IN

Institutional Research Director directs and oversees institutional research and studies for a university/college. Designs and leads institutional research studies evaluating the effectiveness of the organization's programs and policies. Being an Institutional Research Director manages data collection and analysis and oversees the formulation of research reports. May require an advanced degree. Additionally, Institutional Research Director typically reports to a head of a department. The Institutional Research Director manages a departmental sub-function within a broader departmental function. Creates functional strategies and specific objectives for the sub-function and develops budgets/policies/procedures to support the functional infrastructure. Deep knowledge of the managed sub-function and solid knowledge of the overall departmental function. To be an Institutional Research Director typically requires 5+ years of managerial experience. (Copyright 2024 Salary.com)

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Clinical Research Associate (1+ year monitoring experience required)
  • Pharmaceutical Research Associates, Inc
  • Edinburgh, IN OTHER
  • Overview

    Role: Clinical Research Associate

    Location: North of the UK (covering mainly Scotland based sites) 

    Fully sponsor dedicated

     

    ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

     

    With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

     

    Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

    Responsibilities

    As Clinical Research Associate, you will be dedicated to one of our global pharmaceutical clients; a science-based company with one of the most exciting product pipelines in the industry. This global pharmaceutical client develops breakthrough innovative medicines to improve and extend people’s lives in oncology, general medicine and eye care. Working in this way, you will have the opportunity to build your career in a rewarding customer-focused environment that supports creativity, collaboration and performance.

     

     

    Your responsibilities include, but are not limited to: Allocation, initiation and conduct of trials:

    • Conducts site selection for potential sites to evaluate their capabilities for conducting a clinical trial. Recommends sites to participate in clinical trial. Is the frontline liaison between ICON and sites to ensure successful collaboration, meeting ICON expectation on milestone and deliveries
    • Manages assigned study sites and networks, if applicable, conducting phase I-IV protocols according to the monitoring plan and Novartis procedures. Performs Site Initiation Visit, ensures site personnel is fully trained on all trial related aspects. Performs continuous training for amendments and new site personnel as required. Retrains site personnel as appropriate.
    • Conducts continuous monitoring activities (onsite and remote). Implements site management activities to ensure compliance with protocol, GCP, global and local regulations, global and local processes to secure data integrity and patient safety. Is accountable for continuously updating all electronic systems (global and local) relevant to perform job functions.
    • Ensures that study milestones for sites responsible are met as planned (i.e., study startup, recruitment, database analyses, closeout, etc.). Performs Site Closeout activities per SOPs and applicable regulations to ensure that site is aware of any follow up activity and archiving requirements. Attends onboarding-, disease indication and project specific training and general CRA training as required
    • Documents monitoring activities appropriately following ICON standards. Collaborates with the CRA Group Head/CSM to ensure recruitment plans and execute contingency plans,as needed. Participates from audit organization and inspection readiness activities for monitoring and site related activities as required and ensures implementation of corrective actions within specified timelines. Performs additional task as assigned Delivery of quality data and compliance to quality standards
    • Monitors studies as per current legislations, ICH/GCP and Novartis standards. Ensures timely delivery, of high quality, robust and reliable data of the monitored sites to support the goals of Trial Monitoring as defined by Trial Monitoring. (ADIS, DBL). Identifies issues at sites; resolves issues and escalate as appropriate
    • Collaborates with internal stakeholders and site personnel to manage data query resolution process to ensure timely and accurate data entry. Ensures the site Investigator Folder is up to date. Is responsible for collecting essential documents from site and accountable to keep sTMF(s) current. Supports the implementation of innovative processes and technologies Budget and productivity
    • Negotiates investigator remuneration; prepares financial contracts between ICON and investigational sites and investigators. Ensures that payments are appropriately triggered to investigational sites.

    Qualifications

    Degree in scientific or healthcare discipline.• Up to 2 years pharmaceutical industry experience or other relevant experience (NHS or Academic) • Good knowledge of drug development process specifically clinical trial/research• Knowledge of international standards (GCP/ICH, FDA, EMEA)• Monitoring experience is desirable

     

    Important for the role:• Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.• A minimum of 50% overnight travel may be required.

     

    What ICON can offer you:Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.Our benefits examples include:

    • Various annual leave entitlements
    • A range of health insurance offerings to suit you and your family’s needs
    • Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
    • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
    • Life assurance
    • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others

    Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefitsICON, including subsidiaries, is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

  • 25 Days Ago

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Executive Liaison to VPR and Associate Director of Research Operations (Program Management Specialist)
  • Indiana University
  • Bloomington, IN FULL_TIME
  • Department OFC OF IU RESEARCH (UA-VPRO-IUBLA) Department Information The Office of the Vice President for Research at Indiana University is responsible for research development, research compliance, a...
  • 20 Days Ago

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Human Resources Director (Human Resources Leader), IU Research
  • Indiana University
  • Bloomington, IN FULL_TIME
  • Department IU HUMAN RESOURCES (UA-HUMM-IUBLA) Department Information IU Human Resources supports the broader Indiana University academic and research mission, through a wide variety of strategic and o...
  • 23 Days Ago

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Remote data entry
  • Maxion Research
  • Bloomington, IN FULL_TIME
  • Remote Work From Home Data Entry Clerk for Entry Level Position Work at home position for job seekers from virtually any work background who are interested in part-time, side gigs, micro jobs, work fr...
  • 3 Days Ago

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CYBERSECURITY ANALYST - RC
  • McLaughlin Research Corp
  • Crane, IN FULL_TIME
  • Job Description: MRC has an immediate opening for a Cybersecurity Analyst supporting the Naval Surface Warfare Center, Crane Division. This position will provide cybersecurity consulting support to en...
  • 22 Days Ago

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ADMINISTRATIVE ASSISTANT-RC10
  • McLaughlin Research Corp
  • Crane, IN FULL_TIME
  • Job Description: In addition to secretarial duties (filing, taking phone calls, scheduling appointments, making travel arrangements), this position will provide administrative support to executive sta...
  • 23 Days Ago

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0 Institutional Research Director jobs found in Bloomington, IN area

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Assistant/Associate Professor of Clinical Radiology & Imaging Sciences
  • Indiana University
  • Bloomington, IN
  • Title Assistant/Associate Professor of Clinical Radiology & Imaging Sciences Specific Title Musculoskeletal Radiology Ap...
  • 3/29/2024 12:00:00 AM

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Assistant/Associate/Full Professor of Neurological Surgery
  • Indiana University
  • Bloomington, IN
  • Title Assistant/Associate/Full Professor of Neurological Surgery Specific Title Vice Chair of Education and Strategic En...
  • 3/29/2024 12:00:00 AM

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Assistant/Associate/Professor of Clinical Pathology and Laboratory Medicine
  • Indiana University
  • Bloomington, IN
  • Title Assistant/Associate/Professor of Clinical Pathology and Laboratory Medicine Specific Title Clinical Veterinarian A...
  • 3/29/2024 12:00:00 AM

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Executive Director, Convergent Bioscience and Technology Institute
  • Indiana University
  • Bloomington, IN
  • Title Executive Director, Convergent Bioscience and Technology Institute Appointment Status Tenure Track Department IUPU...
  • 3/28/2024 12:00:00 AM

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Psychologist (CBOC)
  • Department of Veterans Affairs
  • Bloomington, IN
  • Summary This position is eligible for the Education Debt Reduction Program (EDRP), a student loan payment reimbursement ...
  • 3/28/2024 12:00:00 AM

Bloomington is a city in and the county seat of Monroe County in the southern region of the U.S. state of Indiana. It is the seventh-largest city in Indiana and the fourth-largest outside the Indianapolis metropolitan area. According to the Monroe County History Center, Bloomington is known as the "Gateway to Scenic Southern Indiana." The city was established in 1818 by a group of settlers from Kentucky, Tennessee, the Carolinas, and Virginia who were so impressed with "a haven of blooms" that they called it Bloomington. The population was 80,405 at the 2010 census. The city's population was ...
Source: Wikipedia (as of 04/11/2019). Read more from Wikipedia
Income Estimation for Institutional Research Director jobs
$80,624 to $121,456
Bloomington, Indiana area prices
were up 1.3% from a year ago

Institutional Research Director in Huntsville, AL
The Office of University Analytics and  Institutional Research is responsible for gathering and analyzing institutional data, providing information and updates to maintain state and federal compliance, and assisting with data requests that advance the university’s overall mission and goals.
February 05, 2020
Institutional Research Director in New Bedford, MA
The Office of Assessment and Institutional Research (AIR) is committed to enhancing the educational, research, and workplace experience at NYU Tandon School of Engineering.
January 14, 2020
Institutional Research Director in Canton, OH
Institutional Research responds to ad hoc requests for data and facilitates training in the use of a data warehouse repository.
January 02, 2020