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Biologic Coordinator Remote Jobs in Indiana (NOW HIRING)

The role combines project coordination, hands-on configuration, training delivery, and customer ... or remote technical seminars. • Resolve software and related hardware issues for current ...

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Biologic Coordinator Remote information

What is a Biologic Coordinator (Remote)?

A Biologic Coordinator (Remote) is a healthcare professional who manages and coordinates the process of obtaining, administering, and monitoring biologic medications for patients, often working from a remote location. They act as a liaison between patients, healthcare providers, insurance companies, and specialty pharmacies to ensure timely access to biologic treatments. Their responsibilities often include insurance verification, prior authorization, patient education, and ongoing support throughout the treatment process. This role requires strong organizational skills, attention to detail, and knowledge of biologic therapies and insurance procedures.

What are some common challenges faced by remote Biologic Coordinators and how can they be addressed?

Remote Biologic Coordinators often face challenges related to communication and coordination with healthcare providers, patients, and insurance companies due to the lack of in-person interactions. Staying organized and using effective digital communication tools are essential to ensure timely medication authorizations and patient support. Building strong relationships with team members and regularly scheduled virtual meetings can help bridge communication gaps. Additionally, remote coordinators must stay updated on changing insurance policies and medication protocols to provide accurate assistance.

What is the difference between Biologic Coordinator Remote vs Clinical Research Coordinator?

AspectBiologic Coordinator RemoteClinical Research Coordinator
CredentialsRelevant certifications (e.g., CCRP, RACB), biology or healthcare backgroundResearch certifications, healthcare or clinical research background
Work EnvironmentRemote, administrative and coordination tasksClinical sites, hospitals, or research facilities
Industry UsagePharmaceutical, biotech, and clinical trial companiesAcademic institutions, hospitals, research organizations
Search IntentRemote biologic trial coordinationOn-site or mixed clinical trial management

The main difference is that a Biologic Coordinator Remote primarily handles biologic clinical trial coordination remotely, focusing on documentation and communication, while a Clinical Research Coordinator often works on-site managing patient visits and data collection. Both roles require similar certifications but differ mainly in work environment and specific responsibilities.

What are the key skills and qualifications needed to thrive as a Biologic Coordinator Remote, and why are they important?

To thrive as a Biologic Coordinator Remote, you need a solid foundation in healthcare coordination, patient advocacy, and knowledge of biologic therapies, often supported by a background in nursing, pharmacy, or medical assisting. Familiarity with health insurance processes, electronic medical records (EMRs), and prior authorization platforms is typically required. Excellent organizational skills, attention to detail, and compassionate communication with patients and providers are essential soft skills. These abilities ensure effective patient support, timely access to biologic treatments, and smooth collaboration across remote healthcare teams.
What are popular job titles related to Biologic Coordinator Remote jobs in Indiana? For Biologic Coordinator Remote jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Biologic Coordinator Remote jobs? Cities in Indiana with the most Biologic Coordinator Remote job openings:
Infographic showing various Biologic Coordinator Remote job openings in Indiana as of July 2026, with employment types broken down into 77% Full Time, 16% Part Time, and 7% Contract. Highlights an 100% Remote job distribution.
Implementation Specialist

Implementation Specialist

STARLIMS

Fort Wayne, IN • On-site, Remote

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 2 days ago


Job description

STARLIMS provides leading Laboratory Information Management System (LIMS) solutions that have served customers around the world for nearly 40 years. Our solution suite helps labs:
  • Improve the reliability of sampling and testing
  • Manage complex testing workflows and analytical methods
  • Simplify compliance and support regulatory standards
  • Unlock comprehensive reporting, monitoring, and analysis
With multiple support centers across the globe, STARLIMS is used in labs across pharma & biotech, food & beverage, petrochemical refineries, oil & gas, chemical, public health, clinical diagnostics, and more, offering you exposure to a wide range of industries and opportunities to grow.
We value people who are curious, accountable, collaborative, and empathetic. Our teams are small, nimble and have a strong drive to succeed. If you are seeking to build your career while working on a technical product that our F500 customers describe as "critical to operational success,", you'll feel at home here.
About the Role:
The MODA-EM Implementation Specialist supports customer software deployments in GMP-regulated environments. You will work directly with clients to understand their QC Microbiology processes, configure and deploy MODA, and serve as a technical resource across the full implementation lifecycle. The role combines project coordination, hands-on configuration, training delivery, and customer support.
What You'll Do:
• Lead customer deployments in GMP-regulated environments, including project coordination, installation, documentation, and validation support.
• Deliver core team training, configuration activities, and end-user / administrative training.
• Conduct product demonstrations and on-site or remote technical seminars.
• Resolve software and related hardware issues for current customers via on-site visits, phone, email, and remote sessions.
• Partner with clients to align operational data, configurations, test methods, and reports with their QC Microbiology workflows.
• Contribute to documentation, training materials, and project plans.
• Manage multiple projects and assignments simultaneously, including pre-sales scoping and sales-to-service transitions.
What We're Looking For:
• Bachelor's degree, preferably in Life Sciences, Lab Systems, or Pharma IT.
• Excellent written and verbal communication, client consulting, and time-management skills.
• Ability to work independently across multiple concurrent projects.
You should have a core background in either QC Microbiology or Laboratory IT Systems, with complementary skills in the other:
QC Microbiology track:
• 3+ years in Quality Control microbiology or a related industry.
• BS in Biology, Microbiology, Chemistry, or related life-science field.
• Beginner-to-intermediate exposure to SQL Server, Oracle, Windows Server, Crystal Reports, Windows 10/11 administration, networking, software/testing lifecycle, or Azure DevOps.
Laboratory IT Systems track:
• 3+ years implementing software systems in regulated laboratory or pharmaceutical production environments (or software engineering experience).
• BS in Computer Science or related IT field.
• Experience implementing QC systems (environmental monitoring, final release, in-process control).
• Hands-on experience with one or more LIMS / lab software platforms such as LabWare, LabVantage SQL*LIMS or Sapphire, ThermoFisher Sample Manager, Novatek NOVA LIMS, Velquest SmartLab, Waters Empower, Labtronics Nexxis ELN, or LIMSLink.
• Foundational scientific knowledge in biology, microbiology, or chemistry, with willingness to deepen domain expertise.
At STARLIMS we offer market competitive benefits such as:
  • Competitive health and Wellness (medical, dental, and vision)
  • Retirement plan with matching company contribution
  • Life Insurance and Disability/Income Protection
STARLIMS is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, creed, religion, color, national or ethnic origin, citizenship, sex, sexual orientation, gender identity and expression, genetic information, veteran status, age or disability status.