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Hourly Adverse Event Reporting Jobs in Indiana (NOW HIRING)

Walgreens

Pharmacist Local Specialty

Indianapolis, IN · On-site

$55.75 - $67/hr

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Walgreens

Pharmacist Local Specialty

Indianapolis, IN · On-site

$55.75 - $67/hr

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Fresenius Medical Care

Registered Nurse

Mishawaka, IN · On-site

Assists the physician in completing and reporting state required adverse event reports and reporting internally as per organization/FMC policy and procedure. MAINTENANCE/TECHNICAL: * Operates ...

WALGREENS

Pharmacist Local Specialty

Indianapolis, IN

$87K - $168K/yr

Confirms pharmacy department employees are trained on all required functions regarding payer and pharmaceutical contractual requirements (adverse event reporting, data and inventory reporting ...

Integrated Resources

Clinical Nurse

Warsaw, IN · On-site

Collect relevant Adverse Event information from clinical databases. Work with clinical sites to collect additional information relevant to complaint reporting and investigation. Perform medical ...

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Hourly Adverse Event Reporting information

What is the difference between Hourly Adverse Event Reporting vs Medical Records Technician?

AspectHourly Adverse Event ReportingMedical Records Technician
CredentialsTypically requires training in adverse event documentation, certifications varyHigh school diploma or equivalent, certification often preferred
Work EnvironmentHealthcare settings, hospitals, clinicsMedical offices, hospitals, healthcare facilities
Job FocusMonitoring, documenting adverse events, complianceManaging patient records, data entry, record organization

Hourly Adverse Event Reporting involves monitoring and documenting adverse events in healthcare, focusing on compliance and patient safety. Medical Records Technicians organize and maintain patient records. While both roles work in healthcare environments, they have different responsibilities and required skills.

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Hourly Adverse Event Reporting jobs near you

Research Nurse Coordinator

Innovative Hematology

Indianapolis, IN • On-site

Other

Posted 24 days ago

Job description

Research Nurse Coordinator

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.

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 includes:

  • Participating in the planning and execution of research projects under the direction of the Medical Director and the primary investigator.
  • Functioning 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.
  • Creating a study budget in InfoED in collaboration with the finance department. Working 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.
  • Assessing patients for inclusion and exclusion criteria to determine study eligibility, and working cooperatively with the comprehensive team to coordinate study-related patient care. Explaining informed consent for each study participant; documenting refusals according to protocol.
  • Ensuring accurate and prompt communication with patients, the primary investigator, research manager, external contacts, study sponsors, and monitors.
  • Preparing study-related documentation such as protocol worksheets, procedural manuals, drug dispensation records, regulatory forms, adverse event reports; submitting all relevant study documents to the institutional review board.
  • Monitoring study activities to ensure compliance with protocols and with all relevant local, federal, and state regulatory and institutional policies. Preparing for or participating in quality assurance audits conducted by study sponsors, federal agencies, or specially designated review groups.
  • Recording adverse event and side effect data and conferring with investigators regarding the reporting of events to oversight agencies.
  • Participating in internal quality assurance; reviewing monitor reports for trends across studies.

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