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Clinical Trial Software Jobs in Indiana (NOW HIRING)

$24 - $26/hr

... phase 2 clinical trial samples and data compilation and review by following standard operating ... Data processing (familiarity with Excel and other graphing software) and accurately recording lab ...

Biologist I

Indianapolis, IN · On-site

$24 - $26/hr

... phase 2 clinical trial samples and data compilation and review by following standard operating ... Data processing (familiarity with Excel and other graphing software) and accurately recording lab ...

Showing results 21-40

Clinical Trial Software information

How does a clinical trial software specialist typically collaborate with clinical research teams during a study?

A Clinical Trial Software Specialist works closely with clinical research coordinators, data managers, and principal investigators to ensure the software aligns with study protocols and regulatory requirements. They are responsible for configuring electronic data capture (EDC) systems, providing user training, troubleshooting technical issues, and ensuring data integrity throughout the trial. This collaborative environment requires strong communication skills and a proactive approach to problem-solving, as the specialist often acts as a liaison between technical and non-technical team members.

What are the key skills and qualifications needed to thrive as a clinical trial software specialist, and why are they important?

To thrive as a Clinical Trial Software Specialist, you need a solid understanding of clinical research processes, data management, and software development principles, often supported by a degree in life sciences, computer science, or a related field. Familiarity with electronic data capture (EDC) systems such as Medidata or Oracle Clinical, knowledge of regulatory compliance like GCP, and sometimes certifications like Certified Clinical Data Manager (CCDM) are typically required. Strong analytical thinking, problem-solving abilities, and effective communication set top performers apart in this role. These skills and qualities are crucial for ensuring accurate data collection, regulatory compliance, and smooth collaboration across clinical research teams.

What is clinical trial software?

Clinical trial software refers to specialized digital tools used to plan, manage, and monitor clinical trials in the medical and pharmaceutical fields. These platforms help streamline processes such as patient recruitment, data collection, regulatory compliance, and reporting. By automating many tasks, clinical trial software increases efficiency, reduces errors, and ensures adherence to industry standards and regulations. This technology is essential for organizations conducting clinical research, as it improves data accuracy and enhances collaboration among stakeholders.

What is the difference between Clinical Trial Software vs Clinical Research Coordinator?

AspectClinical Trial SoftwareClinical Research Coordinator
Primary RoleSoftware tools used to manage, track, and analyze clinical trial dataManages daily activities of clinical trials, including patient recruitment and data collection
Required SkillsTechnical knowledge of software systems, data management, and complianceClinical knowledge, organization, communication, and regulatory understanding
Work EnvironmentTechnology-focused, often in office or remote settingsHospital, clinic, or research facility
Industry UsageUsed by clinical trial teams, data managers, and IT professionalsEmployed directly by research institutions, hospitals, or pharmaceutical companies

While Clinical Trial Software involves the tools used to facilitate and manage clinical trials, Clinical Research Coordinators are the professionals who execute and oversee the trial processes. Both roles are essential in the clinical research industry but serve different functions—one focuses on software solutions, the other on trial management and coordination.

$24 - $26/hr

Full-time

Re-posted 18 days ago


Bureau Veritas rating

8.1

Company rating: 8.1 out of 10

Based on 29 frontline employees who took The Breakroom Quiz

42nd of 120 rated laboratories


Job description

Overview:

Business Title: LEM Biologist I

Position Title: Analyst I

Division: Consumer Products Services

Entity: ATL

Location: Indianapolis, IN

Reports to: Manager

FLSA: Non-exempt

Hours Worked: Typically, Monday through Friday, forty-hours per week.

However, must be flexible to meet the needs of the department and complete other projects as assigned.

Position Summary:

The Biologist will be primarily responsible for the organization, preparation, and analysis of phase 2 clinical trial samples and data compilation and review by following standard operating procedures (SOPs) and protocols. Proper documentation and lab notebooking are essential in this role. Other duties include buffer preparation and general lab upkeep. We are seeking an enthusiastic candidate who has excellent written and communication skills and wants to learn and grow in this role. 

Duties and Responsibilities:

It is everyone's responsibility to live out our Values and Absolutes by Shaping a World of Trust while ensuring responsible progress.

  • Support the implementation of immunogenicity assays and biomarker assays by collaborating with internal scientific/regulatory/quality/clinician subject matter experts (SMEs).
  • Perform experiments to implement assays and analyze samples
  • Draft, compile, and/or review data, protocols and reports
  • Aid in troubleshooting assay issues
  • Ensure assays and analyses comply with most current regulatory agency guidance
  • Manage multiple assay projects and meet timelines established by customers.
  • General laboratory techniques including, but not limited to, pipetting, weighing, and buffer preparation.
  • Familiarity with or willingness to work with automation (liquid handlers, automated Western systems, tube labelers).
  • Data processing (familiarity with Excel and other graphing software) and accurately recording lab activities in an electronic notebook.
  • General laboratory services (inventory, supplies, cleaning, stocking, instrument care and maintenance, and reagent or sample handling).
  • Follow the guidelines set forth with clients and Company Quality, Health, Safety, Security and Environmental policies and procedures.
  • Comply with clients' and Company management systems in accordance with appropriate regulatory agencies.
  • Perform other essential tasks, projects, and responsibilities as required.
  • Other duties as defined by Manager, department needs and workload

Skills & Proficiencies:

  • Must be self-regulated and have high attention to detail for quality and strong organization skills.
  • Ability to understand and execute multi-step protocols.
  • Experience with laboratory documentation practices: recording of information and details necessary to recreate experiment as well as notation of any deviations or errors.
  • Proven Microsoft Word, Excel, Teams, SharePoint, and PowerPoint skills
  • Strong attention to detail and ability to multi-task.
  • Ability to understand the objective of experiments in order to identify issues.
  • Excellent communication skills - verbal and written. Ability to communicate issues as they occur.
  • Works well both as a team and as an individual contributor.
  • Strong safety focus and willingness to assist with general lab housekeeping.
  • Ability and willingness to adapt to changing project needs and timelines and flex plans and responsibilities as needed.
  • Adheres to company values
  • Requires the ability to pass Assay Competency Testing in accordance with regulatory requirements in order to maintain employment

Education and Experience:

  • Degree requirement: Bachelor's Degree in science or a related discipline.

Preferences:

  • Experience in a highly detail-oriented laboratory environment
  • ELISA and liquid handling experience
  • Experimental design; scientific approach to problem solving; method development, optimization, and validation
  • Experience in a regulated (for example, Good Laboratory Practices [GLP], Good Clinical Practices [GCP], Good Manufacturing Practices [GMP]) environment.

 

An equivalent combination of education and experience may be accepted in lieu of above.

Compensation Range: $24.00-$26.00 per hour  (e.g., the job posting is not necessarily reflective of actual compensation that may be earned, and actual compensation is subject to variation due to such factors as location, education, experience, and skillset).


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