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Clemente Clinical Research Jobs (NOW HIRING)

Glaukos

Sr. Clinical Trials Associate

Aliso Viejo, CA

$35.50 - $48.50/hr

The Sr. Clinical Trials Associate is responsible for the coordination of clinical research studies ... Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente ...

Agilidade RH

Gastroenterologist

Aliso Viejo, CA · On-site

$423K/yr

In addition to clinical work, Hoag is committed to building a research footprint. Hoag further ... Aliso Viejo and San Clemente, CA * Conditions: General Gastrointestinal Conditions * Team: IBD ...

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How much do clemente clinical research jobs pay per hour?

As of Jul 27, 2026, the average hourly pay for clemente clinical research in the United States is $22.71, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $25.96 per hour, depending on experience, location, and employer.

What are some common challenges faced by clinical research professionals at Clemente Clinical Research, and how can they be addressed?

At Clemente Clinical Research, professionals often encounter challenges such as managing complex regulatory requirements, coordinating with multiple stakeholders, and ensuring timely data collection. These challenges can be addressed by maintaining clear communication channels within the research team, staying updated on regulatory changes, and utilizing robust project management tools. Collaboration with cross-functional teams and ongoing training also play a key role in overcoming obstacles and ensuring successful clinical trial execution.

What is Clemente Clinical Research?

Clemente Clinical Research refers to a specialized organization or division involved in conducting clinical trials and medical research. These teams typically design, manage, and oversee studies that test new treatments, drugs, or medical devices for safety and effectiveness. Their work is crucial in bringing new therapies to market and improving healthcare outcomes. Clinical research at Clemente may also involve collaboration with hospitals, pharmaceutical companies, and regulatory agencies to ensure studies are ethical and scientifically sound.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate, and why are they important?

To thrive as a Clinical Research Associate, you need a solid background in life sciences or a related field, experience with clinical trial protocols, and often a relevant certification such as ACRP or SOCRA. Familiarity with electronic data capture (EDC) systems, regulatory compliance tools, and Good Clinical Practice (GCP) guidelines is essential. Strong attention to detail, communication, and organizational skills set top performers apart in this role. These competencies ensure accurate data collection, regulatory compliance, and effective coordination across research sites for successful clinical trials.
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Clemente Clinical Research jobs near you
Infographic showing various Clemente Clinical Research job openings in the United States as of July 2026, with employment types broken down into 2% Locum Tenens, 1% Internship, 30% As Needed, and 67% Full Time. Highlights an 100% Physical job distribution, with an average salary of $47,241 per year, or $22.7 per hour.
International Clinical Research Director

International Clinical Research Director

Glaukos

Aliso Viejo, CA

Full-time

Posted 12 days ago

Job description

How You'll Make an Impact:

The Director, Clinical Development - EMEAI serves as the senior regional Clinical Development leader and primary clinical liaison for the EMEAI region. This role supports global clinical development programs across primarily pharmaceutical products, with some combination products, spanning multiple ophthalmology indications. This role supports direct study execution in region, serving as a regional touchpoint for investigators and key opinion leaders and is responsible for local study performance (site identification, activation, enrollment, etc.). 

 

What You'll Do:

  • Serve as the primary Clinical representative for the EMEAI region, providing clinical and regional insight to global clinical development programs.
  • Develop and maintain strong relationships with KOLs and investigators across EMEAI. 
  • Support regional study feasibility, startup, and performance in partnership with regional partners. 
  • Provide regional clinical input into global development strategies, protocols, and study designs. 
  • Collaborate cross-functionally with Regulatory, Biostats/Data Management, Science/Medical Writing, CMC and Global Clinical Operations.
 

How You'll Get There:

  • Extensive experience in pharmaceutical clinical development, with exposure to combination products preferred. 
  • Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions. 
  • Strong understanding of GCP and global clinical development principles. 
  • Driven self-starter
  • Proactively identifies issues/opportunities and delivers solutions
  • Data-driven
  • Relationship-focused; builds strong connections across stakeholders
  • Scientifically inclined-translates complex concepts into actionable study procedures
  • Expert communicator (written and verbal) who builds trust and clarity across teams 
  • 30% travel
 

Education

Advanced degree in a scientific, medical, or health-related discipline
(PhD, PharmD, MD, or equivalent preferred).

#GKOSEMEAI #GKOSINTERNATIONAL   
 

Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible. 

Founded in 1998, Glaukos Corporation is an ophthalmic pharmaceutical and medical technology company focused on developing and commercializing novel therapies for the treatment of glaucoma, corneal disorders, and retinal diseases.

Our mission at Glaukos is to truly transform vision by pioneering novel, dropless therapies that can meaningfully advance the standard of care and improve the lives of patients suffering from chronic, sight-threatening eye diseases. 

Innovation is at the core of everything we do, and we are resolute in our commitment to challenge conventional thinking with new treatment alternatives that are supported by real science, robust clinical evidence, and an unrelenting focus on patients. 

Our constant pursuit of game-changing technologies that disrupt legacy treatment paradigms is encapsulated in the Glaukos mantra "We'll Go First," which articulates our willingness to take chances, our determination to forge new ground, and our commitment to continuous improvement in all that we do.   

Our company completed an initial public offering in June of 2015, and our shares are traded on the New York Stock Exchange under the ticker symbol "GKOS". Our global headquarters is in Aliso Viejo, California with additional locations in San Clemente, California, and Burlington, Massachusetts.

Glaukos Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex including sexual orientation and gender identity, national origin, disability, protected Veteran Status, or any other characteristic protected by applicable federal, state, or local law. 


All offers of employment are contingent upon the successful completion of a background check, including successfully passing a drug screen, based on the position and local regulations.

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