
Job Overview
Location
Lincoln, NE
Job Type
Full-time
Category
Operations
Date Posted
July 9, 2026
Full Job Description
📋 Description
- • Design and develop Standard Operating Procedures (SOPs) that align with company governance and global regulatory requirements.
- • Collaborate with cross-functional teams to ensure SOPs are effective and efficient.
- • Develop and implement training programs to support the adoption of new SOPs.
- • Maintain and update existing SOPs to ensure compliance with changing regulations and company policies.
- • Work with the team in person and on-site every other week, with the option to work primarily from home after 6-8 weeks of on-site training.
- • Utilize experience, agility, and innovative research strategies to help get drugs to market faster.
🎯 Requirements
- • Bachelor's degree in a related field, such as Business Administration, Operations Management, or a related field.
- • 2+ years of experience in a related field, such as Operations, Quality Assurance, or Regulatory Affairs.
- • Strong understanding of regulatory requirements and industry standards.
- • Excellent communication and interpersonal skills.
- • Ability to work independently and collaboratively in a team environment.
- • Proficiency in Microsoft Office, particularly Excel, Word, and PowerPoint.
🏖️ Benefits
- • Competitive salary and benefits package.
- • Opportunities for professional growth and development.
- • Collaborative and dynamic work environment.
- • Flexible work arrangements, including the option to work primarily from home after 6-8 weeks of on-site training.
📍 Location
- • Lincoln, NE
- • On-site work every other week, with the option to work primarily from home after 6-8 weeks of on-site training.
Skills & Technologies
See exactly how your profile matches this role — strengths, skill gaps, and what to do about them.
About Celerion Inc.
Celerion Inc. is a contract research organization providing early-phase clinical research services to the biopharmaceutical industry. Operating facilities in the United States, Canada, and Northern Ireland, the company conducts Phase I and IIa trials, bioanalytical testing, and translational medicine studies. Its core expertise is in pharmacokinetics, pharmacodynamics, and metabolism, supporting the development of small molecules, biologics, and biosimilars for sponsors ranging from emerging biotechs to global pharmaceutical firms.
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