Clinical Research Coordinator
Company: Innovative Hematology, Inc.
Location: Indianapolis
Posted on: February 16, 2026
|
|
|
Job Description:
Job Description Job Description About IHI At Innovative
Hematology, Inc. (IHI), we offer a future where people with rare
blood disorders flourish. Our experts provide the highest quality
comprehensive services and holistic care to patients with bleeding,
clotting and other hematologic disorders, and to their families.
What You Will Do As a Clinical Research Coordinator, you will be
responsible for executing research projects under the direction of
the primary investigator and for performing in accordance to study
regulatory processes, standard operating procedures, and study
protocols. The Opportunity Participate in the planning and
execution of research projects under the direction of the Medical
Director and the primary investigator. Function as an integral part
of the research and comprehensive care teams, working with
colleagues to meet deadlines and maintain a flexible schedule based
on the needs of patients, the department, and IHI. Create a study
budget in InfoED in collaboration with the finance department. Work
with the finance department to assist with billing, invoicing,
tracking status on payments due or past due, documenting patient
stipend requests, and charting completed study visits. Assess
patients for inclusion and exclusion criteria to determine study
eligibility, and work cooperatively with the comprehensive team to
coordinate study-related patient care. Explain informed consent for
each study participant; document refusals according to protocol.
Ensure accurate and prompt communication with patients, the primary
investigator, research manager, external contacts, study sponsors,
and monitors. Prepare study-related documentation such as protocol
worksheets, procedural manuals, drug dispensation records,
regulatory forms, adverse event reports; submit all relevant study
documents to the institutional review board. Monitor study
activities to ensure compliance with protocols and with all
relevant local, federal, and state regulatory and institutional
polices. Prepare for or participate in quality assurance audits
conducted by study sponsors, federal agencies, or specially
designated review groups. Record adverse event and side effect data
and confer with investigators regarding the reporting of events to
oversight agencies. Participate in internal quality assurance;
review monitor reports for trends across studies. Requirements
Minimum Associate’s degree in related field required. Minimum 1
year of related experience required. Valid Indiana Driver’s license
and automobile insurance required. All IHI employees are expected
to enable multi-factor authentication via their personal smart
phone/smart device in order to access IHI systems as a requirement
of the role. Benefits IHI is a not-for-profit program based in
Indianapolis and offers a competitive salary and benefit package.
IHI is the only federally designated comprehensive hemophilia
program in Indiana and serves the entire state through services
available in Indianapolis and at outreach clinics. IHI is a leader
in hemophilia care, education and clinical research and has a
dedicated on-site multidisciplinary staff to ensure availability of
a wide range of required services. IHI participates in national and
international clinical research, including new infusion products
and therapies, investigation of long-term outcomes, and the impact
of associated conditions. The IHI research program provides
patients access to new therapies, and an opportunity to improve
care. Our center has more than 50 clinical research projects
involving bleeding disorders, sickle cell disease, thrombosis and
more. Innovative Hematology, Inc. is an Equal Opportunity
Employer.
Keywords: Innovative Hematology, Inc., Bloomington , Clinical Research Coordinator, Science, Research & Development , Indianapolis, Indiana
