1

Contract Research Jobs in Indiana (NOW HIRING)

Counsels, directs, and/or assists faculty, staff, and researchers in matters related to preparation ... WORK EXPERIENCE Required * 2 years in grants, contracts, and/or research policy related field.

New

Lead Contract Negotiations: Develop and execute strategies to secure favorable terms and manage ... S. Through use of groundbreaking research and advanced technology, our highly skilled employees ...

Substantial Contract to Cash experience in SAP. Responsibilities: * Research and analyze pricing and contract data. * Partner with key stakeholders, including the Strategic Deal Team, Corporate ...

P. is seeking a Contract Insurance Specialist. This position will report to our Sr. Vice President ... Research applicable laws and remain abreast of changes with our corporate insurance program.

Research, develop and write basic contracts or contract changes to meet regulatory and/or business needs and timelines * Collaborate with business line on filing strategies and materials * Review and ...

Showing results 41-60

Contract Research information

What are the key skills and qualifications needed to thrive as a contract research associate?

To thrive as a Contract Research Associate, you need a background in life sciences or a related field, strong research methodology knowledge, and often a relevant degree (such as a BSc or MSc). Familiarity with clinical trial management systems (CTMS), Good Clinical Practice (GCP) certification, and data analysis tools like SPSS or SAS are typically required. Attention to detail, strong organizational skills, and effective communication are vital soft skills for coordinating studies and managing stakeholders. These abilities ensure high-quality, compliant research execution and reliable study outcomes within regulatory frameworks.

What is contract research?

Contract research refers to research services provided by an external organization, known as a Contract Research Organization (CRO), to other businesses, academic institutions, or government agencies. These services often include conducting clinical trials, laboratory testing, data analysis, or product development on a contractual basis. Contract research allows companies to access specialized expertise, reduce costs, and focus on their core activities while outsourcing complex or resource-intensive research tasks.

What are some common challenges faced by professionals in contract research roles and how can they be managed?

Professionals in contract research often navigate tight deadlines, shifting client requirements, and the need to maintain strict regulatory compliance. Balancing multiple projects simultaneously and communicating effectively with both internal teams and external sponsors can be demanding. Proactively managing workload, staying organized, and maintaining clear, consistent communication with stakeholders are key strategies to overcome these challenges. Additionally, staying updated on industry regulations and leveraging project management tools can help ensure successful outcomes.
What are the most commonly searched types of Research jobs in Indiana? The most popular types of Research jobs in Indiana are:
What are popular job titles related to Contract Research jobs in Indiana? For Contract Research jobs in Indiana, the most frequently searched job titles are:
What cities in Indiana are hiring for Contract Research jobs? Cities in Indiana with the most Contract Research job openings:
Infographic showing various Contract Research job openings in Indiana as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 85% Full Time, 11% Part Time, and 2% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution.

ELN Administrator (Bioanalytical Support)

B2S Life Sciences LLC

Franklin, IN • On-site

Full-time

Re-posted 25 days ago


Job description

Description:

Location: Onsite in Franklin, Indiana.



Position Summary

The ELN Administrator is responsible for the management, creation, maintenance, and continuous improvement of Electronic Lab Notebook (ELN) templates used at B2S LifeSciences workflows within a regulated Contract Research Organization (CRO). This role supports scientific and operational teams by translating study protocols, assay methods, and regulatory requirements into standardized, compliant, and user-friendly electronic templates to support our Logistics, Metrology, Chemical Reagent Team, and Bioanalytical groups.

The ELN Administrator serves as the Technical Lead and SME (Subject Matter expert) for the Sapio ELN platform.

The position plays a critical role in ensuring data integrity, consistency, and efficiency in bioanalytical study execution, while maintaining compliance with GLP, GCP, and 21 CFR Part 11 requirements.



Key Responsibilities

ELN Template Development & Maintenance

  • Design, build, and maintain ELN templates for ligand binding assays, including PK, immunogenicity (ADA), and biomarker workflows.
  • Design, build, and maintain ELN templates for Critical Reagent workflows.
  • May require user to translate study protocols, assay methods, and SOPs into structured, standardized ELN formats.
  • Ensure templates support accurate, complete, and consistent data capture.
  • Maintain version control and lifecycle management of ELN templates.
  • Serves as a Subject Matter Expert (SME) for ELN Template generation, qualification and implementation within a regulatory environment.
  • Other duties as assigned.

Regulatory Compliance & Data Integrity

  • Ensure all ELN templates comply with GLP, GCP, and 21 CFR Part 11 requirements for electronic records and signatures. Other regulations may apply.
  • Partner with Quality Assurance (QA) to ensure templates meet audit and inspection readiness standards.
  • Incorporate data integrity principles (ALCOA+) into all template designs.
  • Support audit preparation and responses related to ELN processes.

Cross-Functional Collaboration

  • Work closely with various B2S team members to understand workflow requirements.
  • Collaborate with IT and ELN system administrators (internally & externally) to implement template functionality and updates.

Process Improvement & Standardization

  • Identify opportunities to improve template usability, automation, and efficiency.
  • Drive standardization across assays, studies, and clients where appropriate.
  • Contribute to SOP development and best practices for ELN usage.

User Support & Training

  • Provide guidance and support to laboratory staff on ELN template usage, training and deployment.
  • Assist in troubleshooting template-related issues.
  • Develop training materials and conduct user training sessions as needed.

Documentation & Change Management

  • Manage template change requests and document all updates in accordance with change control procedures.
  • Maintain clear documentation of template specifications and configurations.
  • Other duties as assigned.
Requirements:

Education

  • Bachelor’s degree in Life Sciences, Chemistry, Biology, or a related field or equivalent combination of scientific and administrative experience.

Experience

  • 2–5+ years of experience in a regulated laboratory, CRO, or pharmaceutical environment.
  • Experience working with Electronic Lab Notebooks (e.g., IDBS E-Workbook, Benchling, LabWare ELN, or similar. Sapio Is preferred).
  • Experience in developing Electronic Lab Notebook templates is preferred.
  • Familiarity with bioanalytical workflows, preferably ligand binding assays.

Technical Skills

  • Strong attention to detail with the ability to translate scientific procedures into structured digital templates.
  • Proficiency in data structuring, formatting, and workflow logic.
  • Experience with document control and versioning systems.
  • Basic understanding of assay workflows (ELISA, MSD, etc.) is highly desirable.

Regulatory Knowledge

  • Understanding of GLP, GCP, and 21 CFR Part 11 requirements.
  • Familiarity with data integrity principles (ALCOA+).


Preferred Qualifications

  • Experience specifically supporting ligand binding assay (LBA) environments (PK, ADA, biomarkers).
  • Experience using an Electronic Laboratory Notebook system, generation and versioning of templates and Exposure to LIMS and other laboratory informatics systems.
  • Experience with validation of computerized systems (CSV) or template validation.
  • Prior experience in template automation or workflow optimization.


Key Competencies

  • Exceptional attention to detail and organizational skills
  • Strong written and verbal communication
  • Ability to collaborate across scientific, QA, and IT teams
  • Problem-solving and process improvement mindset
  • Adaptability in a fast-paced, regulated environment
  • Commitment to quality and compliance


Work Environment

  • Office or hybrid role within a CRO supporting laboratory operations.
  • Frequent interaction with laboratory scientists, QA, and IT teams.
  • Work may be deadline-driven, aligned with study start-up timelines.