Indiana Other Job Listings

Be Part of the Science That Keeps Communities Strong (Evansville)64843003350275120

Craigslist

Be Part of the Science That Keeps Communities Strong (Evansville)

Trialmed Evansville is looking for overall healthy volunteers to participate in a clinical research trial to help advance vaccine research. • 50 to 64 years old • Health status is further evaluated by reviewing medical history, screening assessments, and visit with physician • Available and willing to commit to the trial visit structure - You will be asked to come to our clinic for 3 outpatient visits and 3 follow-up phone calls Participants must be generally healthy and NOT at risk for severe COVID-19. Study participants must NOT have any of the following: • Asthma • Obesity (BMI > 30 kg/m2) • Type 1 or Type 2 Diabetes Mellitus • Any Heart Conditions (heart failure, coronary artery disease (CAD), or cardiomyopathies) • Chronic Lung Disease (COPD, interstitial lung disease, pulmonary embolism, pulmonary hypertension) • Mental health conditions such as schizophrenia, mood disorders, major depression • Current or former smoker Eligible participants will receive trial related care and assessments at no cost and may be compensated up to $414 for trial related time. If you are interested in participating, please complete the contact form. We will follow up with more information and schedule an appointment to see if you qualify. Additional Details

955 S Kenmore Dr, Evansville, IN 47714, USA

$414/day

Do you drink alcohol? We want to study your brain! (Payment offered) (Indianapolis)64634682214401121

Craigslist

Do you drink alcohol? We want to study your brain! (Payment offered) (Indianapolis)

Thank you for your interest in our studies! Some of our studies involve an MRI where we take pictures of your brain, some involve alcohol delivered to you through an IV, and some involve tasting beverages, alcoholic and non-alcoholic, while in the MRI scanner. One study involves an overnight visit. If you qualify after the initial phone interview, you will be invited to a paid, in-person interview at Goodman Hall in Downtown Indianapolis. If you qualify after the in-person interview and agree to participate, then you will be scheduled for a paid study day. Participants may earn up to $325 or $575 for completion of an interview (approximately 3 hrs.) and study visit, depending on the study for which you are qualified. Some study visits may require an overnight stay (approximately 24 hours) at University Hospital in Downtown Indianapolis, while others only require participation for a 6½ hour visit during normal business hours. To see if you qualify, please complete this survey: https://redcap.uits.iu.edu/surveys/?s=YAWFYJ7CTN or call (317) 278-5010 for a phone interview. David Kareken, Ph.D., study principal investigator

1340 Cora St, Indianapolis, IN 46202, USA

$325-575/week

Research Nurse Coordinator63392007129475122

Workable

Research Nurse Coordinator

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 Research Nurse 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 Nursing. Bachelor’s preferred RN or LPN license in the state of Indiana required Minimum 5 years of related experience Experience in pharmaceutical sponsored studies required Valid Indiana Driver’s license and automobile insurance 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.

Indianapolis, IN, USA

Negotiable Salary

Clinical Research Coordinator63500033163523123

Workable

Clinical Research Coordinator

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.

Indianapolis, IN, USA

Negotiable Salary