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Clinical Study Designer Jobs (NOW HIRING)

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ... Experience in study designs for in vitro diagnostic technologies (IVD) is highly preferred ...

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU ... Experience in study designs for in vitro diagnostic technologies (IVD) is highly preferred ...

Danaher

Senior Clinical Study Manager

Chaska, MN · On-site

$135K/yr

Experience in study designs diagnostic technologies (IVD) is highly preferred, specifically for Clinical Chemistry, Immunoassays, and/or Biomarkers. * Advanced degree in Science, Healthcare, or ...

Danaher

Senior Clinical Study Manager

Chaska, MN · On-site

$135K/yr

Experience in study designs diagnostic technologies (IVD) is highly preferred, specifically for Clinical Chemistry, Immunoassays, and/or Biomarkers. * Advanced degree in Science, Healthcare, or ...

Arthrex GmbH

Sr. Clinical Study Manager

Naples, FL · On-site

... is designed to collect all required data per the protocol. * Responsible for training internal ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.

ARTHREX

Sr. Clinical Study Manager

Naples, FL · On-site

... is designed to collect all required data per the protocol. * Responsible for training internal ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.

Arthrex

Sr. Clinical Study Manager

Naples, FL · On-site

... is designed to collect all required data per the protocol. * Responsible for training internal ... Prepare and track clinical study budgets that include both sponsor costs and sites costs.

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Clinical Study Specialist

Cambridge, MA · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON is a global ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Specialist

Cambridge, MA · Hybrid

$62K - $77K/yr

Clinical Study Specialist - Hybrid role: Warren, NJ, Armonk NY or Cambridge MA ICON is a global ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Specialist

New York, NY · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid - Warren, NJ, Armonk, NY or Cambridge MA)) ICON is a global ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Specialist

Warren, NJ · Hybrid

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

ICON

Clinical Study Specialist

Warren, NJ · On-site

$62K - $77K/yr

Clinical Study Specialist (Hybrid office/home based in Warren NJ, Armonk NY or Cambridge MA) ICON ... Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to ...

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Clinical Study Designer information

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How much do clinical study designer jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for clinical study designer in the United States is $37.67, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $48.08 per hour, depending on experience, location, and employer.

What does a clinical study designer do?

A Clinical Study Designer is responsible for planning, structuring, and developing the protocols for clinical trials. They work to ensure that studies are scientifically sound, ethically conducted, and compliant with regulatory requirements. Their tasks include defining study objectives, selecting methodologies, determining sample sizes, and coordinating with cross-functional teams. This role is critical in ensuring that clinical studies produce reliable data to evaluate the safety and efficacy of new drugs or treatments.

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

To thrive as a Clinical Study Designer, you need a solid background in clinical research, study protocol development, and regulatory compliance, typically supported by a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, statistical software (such as SAS), and GCP certifications are commonly required. Strong analytical thinking, attention to detail, and effective communication skills help ensure the clarity and integrity of study designs. These skills and qualifications are essential for producing rigorous, compliant studies that yield reliable, actionable results in clinical research.

What are some common challenges clinical study designers face when working on multi-center trials?

Clinical Study Designers often encounter challenges in ensuring protocol consistency and regulatory compliance across multiple study sites. Coordinating timelines, managing varying site capabilities, and facilitating clear communication between diverse teams can be complex. To address these challenges, designers rely on robust project management tools, detailed documentation, and regular cross-site meetings. Collaborative skills and adaptability are essential for maintaining study integrity and achieving successful trial outcomes.

What are popular job titles related to Clinical Study Designer jobs?

For Clinical Study Designer jobs, the most frequently searched job titles are:

Clinical Study Designer - Lincoln, Nebraska

Lincoln, NE

Celerion
Pharmaceutical and Medicine Manufacturing • 1 - 5K employees
Learn more about Celerionexternal

$20 - $21/hr

Full-time

Re-posted 15 days ago

Celerion rating

7.0

Company rating: 7.0 out of 10

Based on 13 frontline employees who took The Breakroom Quiz

64th of 75 rated research

Job description

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

We are currently seeking a full time Clinical Study Designer at our Lincoln, Nebraska location.  As part of our team, you will be responsible for the logistical set up and maintenance of clinical trials in ClinQuick - our electronic data capture system. You will also manage the creation of study conduct instruction manuals and detailed timed event schedules for the clinic staff and study participants. 
 
Requirements:
A minimum of an Associate’s degree in a health related field and/or applicable experience in a medical, clinical, pharmaceutical or laboratory setting is required. You must be detail‑oriented, computer literate, and able to work in a fast-paced atmosphere.
Celerion Values:       Integrity   Trust   Teamwork   Respect
 
Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.
 

Note: To make sure you don't miss important updates from us, please check your Spam folder for emails from @celerion.com, particularly interview invitations. If you find one there, mark it as "Not Junk" to ensure future Celerion emails land in your inbox. Please note that Gmail accounts have been particularly noted as routing to Spam.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.

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