ZipRecruiter

Log In

1

Clinical Research Position Jobs in Indiana (NOW HIRING)

Actalent

Research Navigator

Indianapolis, IN

$28 - $35/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Clinical Research Navigator (Oncology) Contract-to-Hire | Hybrid Schedule We are seeking a Clinical ... Pay and Benefits The pay range for this position is $28.00 - $35.00/hr. Eligibility requirements ...

Becton, Dickinson and Company

  • Medical

  • Life

WAT), by applying to this role, you will be applying for a position with Waters. Waters is a global ... Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ...

Icon plc

Clinical Research Associate

Indianapolis, IN

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Clinical Research Associate ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values ...

Versiti, Inc.

Clinical Research Support - IN

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position SummaryUnder the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...

Versiti, Inc.

Clinical Research Support - IN

Indianapolis, IN · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Position Summary Under the direction of department leadership, Assistant, Clinical Research is responsible for handling a variety of administrative tasks associated with research studies including ...

previous page

Showing results 41-60

All JobsClinical Research Position JobsClinical Research Position Jobs in Indiana

Clinical Research Position information

What is a clinical research position?

A clinical research position typically involves planning, coordinating, and conducting research studies that test new medical treatments, drugs, or devices in human participants. Professionals in these roles may work in hospitals, universities, or pharmaceutical companies to ensure that studies are ethically conducted and compliant with regulatory standards. Their responsibilities can include recruiting participants, collecting and analyzing data, and maintaining documentation. These positions are vital for advancing medical knowledge and improving patient care.

How does a clinical research professional typically collaborate with healthcare providers and regulatory teams during a clinical trial?

Clinical research professionals work closely with healthcare providers, such as physicians and nurses, to ensure that study protocols are followed and that patient safety is maintained throughout the trial. They also interact regularly with regulatory teams to ensure compliance with local and international regulations, assisting with the preparation and submission of necessary documentation. Effective communication and collaboration are essential, as clinical research professionals act as a bridge between the research team, clinical staff, and regulatory authorities to facilitate smooth trial execution.

What are the key skills and qualifications needed to thrive in a clinical research position, and why are they important?

To thrive in a Clinical Research Position, you need a solid understanding of clinical trial protocols, regulatory compliance, and data analysis, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture systems, clinical trial management software (CTMS), and certifications such as Good Clinical Practice (GCP) are commonly required. Strong attention to detail, effective communication, and the ability to collaborate across multidisciplinary teams help professionals excel in this field. These skills are critical for ensuring accurate data collection, regulatory adherence, and successful execution of clinical studies.

What is the difference between Clinical Research Position vs Clinical Research Coordinator?

AspectClinical Research PositionClinical Research Coordinator
CredentialsVaries; often includes degrees in health sciences, certifications like CCRPTypically requires a bachelor's degree in health or life sciences, certification preferred
Work EnvironmentResearch labs, pharmaceutical companies, academic institutionsHospitals, clinics, research sites
Employer & Industry UsageUsed across biotech, pharma, academiaCommonly employed in clinical trial sites and hospitals
Job FocusDesigning, managing, and analyzing clinical studiesOverseeing daily trial activities, patient coordination

The Clinical Research Position generally involves higher-level responsibilities like study design and data analysis, often requiring advanced certifications. The Clinical Research Coordinator focuses on managing daily trial operations and patient interactions at research sites. Both roles are essential in clinical research but differ in scope and responsibilities.

What do you do as a clinical research position?

A clinical research position involves designing, conducting, and managing clinical trials to evaluate the safety and effectiveness of medical treatments or devices. Professionals in this role collect and analyze data, ensure compliance with regulatory standards, and often work with healthcare teams and research protocols. Strong organizational skills and knowledge of Good Clinical Practice (GCP) are essential for success in this field.

What qualifications do you need to be a clinical research position?

To qualify for a clinical research position, candidates typically need a bachelor's degree in a health-related field such as biology, nursing, or pharmacy. Relevant skills include knowledge of Good Clinical Practice (GCP), attention to detail, and experience with data management or clinical trial protocols; some roles may require certification like the Certified Clinical Research Professional (CCRP).

What are popular job titles related to Clinical Research Position jobs in Indiana?

For Clinical Research Position jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Clinical Research Position jobs in Indiana look for?

The top searched job categories for Clinical Research Position jobs in Indiana are:

What cities in Indiana are hiring for Clinical Research Position jobs?

Cities in Indiana with the most Clinical Research Position job openings:

Clinical Research Position jobs near you

Clinical Research Data Entry Specialist

ObjectiveHealth

South Bend, IN

Full-time

Posted 25 days ago

Job description

Description

Clinical Research Data Entry Specialist (Onsite)

The Clinical Research Data Entry Specialist is responsible for accurately entering, reviewing, and maintaining clinical trial data in EDC systems. This role supports clinical research studies by ensuring data quality, completeness, and compliance with study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements. This position is ideal for a detail-oriented individual with data entry or administrative experience who is interested in building a career in clinical research. 


 ObjectiveHealth is a clinical research company transforming how research is conducted at the point of care. Using our proprietary technology, we aim to:

  • Increase patient access to research trials within our communities
  • Provide physicians with enhanced care options for current patients
  • Deliver superior clinical research enrollment metrics to Pharma sponsors

All with the ultimate goal of Improving Patient Outcomes at the Point of Care. We want you to join us in doing just that.


 Key Responsibilities:

  • Enter clinical trial data into Electronic Data Capture (EDC) systems accurately and within required timelines. 
  • Review source documents and medical records to ensure complete and accurate transcription of participant data. 
  • Verify data for accuracy, completeness, and consistency prior to submission. 
  • Review, investigate, and resolve EDC data queries generated by sponsors, contract research organizations (CROs), or data management teams by comparing source documentation and collaborating with study personnel. 
  • Communicate with Clinical Research Coordinators, investigators, and other study staff to resolve missing, incomplete, or inconsistent data. 
  • Correct data discrepancies while maintaining appropriate documentation and audit trails within the EDC system. 
  • Ensure timely completion of data entry and query resolution to support study milestones and database lock. 
  • Maintain accurate study documentation related to data entry activities. 
  • Adhere to study protocols, sponsor requirements, Good Clinical Practice (GCP), HIPAA, and applicable regulatory guidelines. 
  • Assist with quality control reviews and support sponsor monitoring visits, audits, and regulatory inspections as needed. 
  • Maintain confidentiality of participant information and research data. 

Qualifications:

  • High school diploma or equivalent. 
  • 1+ years of data entry, administrative support, medical office, or related experience. 
  • Excellent attention to detail and data accuracy. 
  • Strong organizational and time management skills. 
  • Ability to manage multiple priorities and meet deadlines in a fast-paced environment. 
  • Strong written and verbal communication skills.

Requirements

This job requires legal authorization to work in the US. We are not currently accepting work visas. ObjectiveHealth is an EEO Employer and an E-Verify participant 

Apply