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Clinical Study Manager Jobs in Nebraska (NOW HIRING)

Argenta

Study Director - Americas CRO

Oakland, NE · On-site

Advanced degree in a scientific discipline. * 10+ years experience in animal health product development, or veterinary clinical study project management. * Proven experience managing cross functional ...

Argenta

Study Director - Americas CRO

Oakland, NE · On-site

Advanced degree in a scientific discipline. * 10+ years experience in animal health product development, or veterinary clinical study project management. * Proven experience managing cross functional ...

Argenta

Study Director - Americas CRO

Oakland, NE

Advanced degree in a scientific discipline. * 10+ years experience in animal health product development, or veterinary clinical study project management. * Proven experience managing cross functional ...

Celerion

Clinical Research Coordinator

Lincoln, NE · On-site

$21 - $28/hr

You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies ...

Celerion

Clinical Research Coordinator

Lincoln, NE · On-site

$21 - $28/hr

You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies ...

Celerion

Clinical Research Coordinator

Lincoln, NE

$21 - $28/hr

You are responsible for the overall management of Clinical Studies to include: on-time performance with defect-free execution, independently conducting bioequivalency and bioavailability studies ...

micro1 AI

Medical Writing Manager

Omaha, NE · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

micro1 AI

Medical Writing Manager

Lincoln, NE · Remote

$50 - $80/hr

Author and review realistic evaluation tasks based on Clinical Study Reports, DSURs, PSURs/PBRERs ... and appendix management. * Evaluate scientific accuracy in narrative sections such as efficacy ...

Bryan Health

Clinical Nurse Specialist

Lincoln, NE · On-site

Provides routine or urgent care management for complex, high-risk patients/families to improve patient outcomes, investigate clinical practice issues, generate clinical study/research questions ...

Bryan Health

Clinical Nurse Specialist

Lincoln, NE · On-site

Provides routine or urgent care management for complex, high-risk patients/families to improve patient outcomes, investigate clinical practice issues, generate clinical study/research questions ...

Bryan Health

Clinical Nurse Specialist

Lincoln, NE · On-site

Provides routine or urgent care management for complex, high-risk patients/families to improve patient outcomes, investigate clinical practice issues, generate clinical study/research questions ...

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Showing results 21-40

All JobsClinical Study JobsClinical Study Manager JobsClinical Study Manager Jobs in Nebraska

Clinical Study Manager information

See Nebraska salary details

$27

$59

$91

How much do clinical study manager jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for clinical study manager in Nebraska is $59.61, according to ZipRecruiter salary data. Most workers in this role earn between $48.37 and $67.16 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical study manager?

To thrive as a Clinical Study Manager, you need a strong background in clinical research, project management, and regulatory compliance, typically supported by a degree in life sciences and experience in clinical trials. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications like GCP (Good Clinical Practice) are highly valued. Strong organizational, leadership, and communication skills help manage cross-functional teams and ensure study timelines are met. These skills are crucial for maintaining study quality, ensuring regulatory adherence, and delivering successful trial outcomes.

What are some common challenges faced by clinical study managers, and how can they be addressed?

Clinical Study Managers often encounter challenges such as coordinating multiple stakeholders, ensuring regulatory compliance, and managing tight timelines across study sites. Effective communication and proactive planning are essential to address these issues, as well as staying up to date with changing industry regulations. Building strong relationships with site staff and fostering a collaborative team environment can also help mitigate delays and ensure study milestones are met successfully.
What are the most commonly searched types of Clinical Study jobs in Nebraska? The most popular types of Clinical Study jobs in Nebraska are:
What are popular job titles related to Clinical Study Manager jobs in Nebraska? For Clinical Study Manager jobs in Nebraska, the most frequently searched job titles are:
What job categories do people searching Clinical Study Manager jobs in Nebraska look for? The top searched job categories for Clinical Study Manager jobs in Nebraska are:
What cities in Nebraska are hiring for Clinical Study Manager jobs? Cities in Nebraska with the most Clinical Study Manager job openings:
Clinical Study Manager jobs near you
Infographic showing various Clinical Study Manager job openings in Nebraska as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 15% Part Time, and 1% Contract. Highlights an 93% Physical, 3% Hybrid, and 4% Remote job distribution, with an average salary of $123,981 per year, or $59.6 per hour.

Study Director - Americas CRO

Argenta

Oakland, NE • On-site

Full-time

Re-posted 5 days ago

Job description

At Argenta, we're more than a company - we're a global team, dedicated to healthier animals. We believe that when their lives are made better, we're all the better for it.
Founded in 2006, we support companies big and small to develop and manufacture health products for pets and livestock. Our trusted, innovative solutions and services cover every stage of the process, from molecule to market.
We're in a unique position. We are the world's only combined contract research and contract development and manufacturing organization (CRO/CDMO) dedicated to animal health.
Our uniqueness means:
We are ambitious, growing and building a 'one team' culture, guided by our values.
    • We are team players;
    • We are doers;
    • We are customer-centric;
    • We are innovators.

We value diversity, as a global company, we get the richness of working with different people in different places whether it be location, stages of their career, their development, their role. We believe that when everyone works together and puts their best "paw" forward we will make the lives of the animals we care for, better.
With bases in New Zealand, the US, the UK and Europe, our 900+ colleagues are driven by our partnership approach and purpose: Healthy Animals. Let's Make It Happen, Together.
TEAM PLAYERS who want to DO great work and find INNOVATIVE ways to make animals lives better through our CUSTOMER CENTRIC efforts should apply.
Argenta is currently looking to fill the role of Study Director at our Oakland, NE location.
Key Responsibilities
  • Approve and sign study protocol
  • Ensure objectives meet regulatory requirements
  • Coordinate with Sponsors and Quality Assurance
  • Delegates tasks accordingly during the course of the study but retails full responsibility
  • Ensures the study follows GLP and study protocol, overseeing animal care, sample collection and data recording
  • Addresses deviations and ensures proper documentation
  • Review and interpret results ensuring the scientific validity of conclusions
  • Writes, approves and signs the final study report
  • Ensures all raw data are archived properly

About You
  • Advanced degree in a scientific discipline.
  • 10+ years experience in animal health product development, or veterinary clinical study project management.
  • Proven experience managing cross functional teams
  • Thorough knowledge of practical experience in GLP protocols, Final Study Reports and Study Master Files
  • Collaborative working style and the ability to lead and motivate people at all levels and across multiple functions within the organization
  • Proven affinity with Animal Health
  • Excellent attention to detail and scientific judgement

Argenta has strongly embedded company values which is key to who we are and how we deliver. We offer an opportunity to work for a successful and rapidly expanding global business where your input will be valued. At Argenta we are a hard-working group who really enjoy the people we work with each day. That is why we support our people through a strong culture, great benefits, and growth opportunities.
Argenta is an equal-opportunity employer
To find out more about Argenta, click here: www.argentaglobal.com

Apply