Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions. * Strong understanding of GCP and global clinical development ...
Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions. * Strong understanding of GCP and global clinical development ...
Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions. * Strong understanding of GCP and global clinical development ...
Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions. * Strong understanding of GCP and global clinical development ...
As a Clinical Research Project Director, you will provide strategic leadership for complex global ... Working in a collaborative, international environment, you will guide cross-functional teams ...
As a Clinical Research Project Director, you will provide strategic leadership for complex global ... Working in a collaborative, international environment, you will guide cross-functional teams ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
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As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Bachelor's degree, or its international equivalent in a scientific or health-related field or an ...
Must meet all requirements for Principal Clinical Research Associate position and have demonstrated ... Must be able to resolve problems using national and international regulations, guidelines, and ...
Must meet all requirements for Principal Clinical Research Associate position and have demonstrated ... Must be able to resolve problems using national and international regulations, guidelines, and ...
Clinical Research Assistant
Brownsville, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
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Clinical Research Assistant
Brownsville, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
Clinical Research Assistant
San Antonio, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
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Clinical Research Assistant
San Antonio, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
Clinical Research Assistant
Austin, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
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Clinical Research Assistant
Austin, TX · On-site
... International Council for Harmonization Good Clinical Practice (ICH GCP), Health Insurance ... Clinical research certification preferred Knowledge, Skills, and Other Abilities: * Ability to ...
Clinical & Endpoint Research Associate
Aurora, CO · On-site
$60K - $70K/yr
The Clinical & Endpoint Research Associate supports site operations with a primary focus on domestic and international travel to complete Site Endpoint Evaluation Visits (SEEVs) and assists with ...
Clinical & Endpoint Research Associate
Aurora, CO · On-site
$60K - $70K/yr
The Clinical & Endpoint Research Associate supports site operations with a primary focus on domestic and international travel to complete Site Endpoint Evaluation Visits (SEEVs) and assists with ...
The Clinical & Endpoint Research Associate supports site operations with a primary focus on domestic and international travel to complete Site Endpoint Evaluation Visits (SEEVs) and assists with ...
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The Clinical & Endpoint Research Associate supports site operations with a primary focus on domestic and international travel to complete Site Endpoint Evaluation Visits (SEEVs) and assists with ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing ... Provide oversight of domestic and international clinical supply shipments. Communicate with trial ...
Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing ... Provide oversight of domestic and international clinical supply shipments. Communicate with trial ...
Position Details Position Information Recruitment/Posting Title Assoc. Dir Research Operations ... Global clinical research experience and familiarity with international regulatory expectations.
Position Details Position Information Recruitment/Posting Title Assoc. Dir Research Operations ... Global clinical research experience and familiarity with international regulatory expectations.
... all aspects of international clinical trials within designated program budgets and timelines ... Must meet all requirements for Principal Clinical Research Associate position and have demonstrated ...
... all aspects of international clinical trials within designated program budgets and timelines ... Must meet all requirements for Principal Clinical Research Associate position and have demonstrated ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
Quick apply
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
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As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
CLINICAL RESEARCH COORDINATOR
Durham, NC · On-site
$22 - $29.25/hr
May maintain study level documentation for international studies and develop resources and tools ... Minimum Qualifications Education Completion of an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR
Durham, NC · On-site
$22 - $29.25/hr
May maintain study level documentation for international studies and develop resources and tools ... Minimum Qualifications Education Completion of an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR
Durham, NC · On-site
$22 - $29.25/hr
May maintain study level documentation for international studies and develop resources and tools ... Minimum Qualifications Education Completion of an Associate's degree Experience Work requires a ...
CLINICAL RESEARCH COORDINATOR
Durham, NC · On-site
$22 - $29.25/hr
May maintain study level documentation for international studies and develop resources and tools ... Minimum Qualifications Education Completion of an Associate's degree Experience Work requires a ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
Quick apply
As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ... Ability to travel at least 60% of the time (international and domestic - fly and drive) and should ...
Associate International Clinical Research information
See salary details
$36K - $45.8K
8% of jobs
$45.8K - $55.5K
8% of jobs
$60.4K is the 25th percentile. Wages below this are outliers.
$55.5K - $65.3K
17% of jobs
$65.3K - $75.1K
10% of jobs
$75.1K - $84.9K
3% of jobs
The median wage is $94.6K / yr.
$84.9K - $94.6K
3% of jobs
$94.6K - $104.4K
6% of jobs
$104.4K - $114.2K
8% of jobs
$114.2K - $124K
7% of jobs
$125.3K is the 75th percentile. Wages above this are outliers.
$124K - $133.7K
23% of jobs
$133.7K - $143.5K
5% of jobs
$36K
$94.3K
$143.5K
How much do associate international clinical research jobs pay per year?
What is the difference between Associate International Clinical Research vs Clinical Research Coordinator?
| Aspect | Associate International Clinical Research | Clinical Research Coordinator |
|---|---|---|
| Required Credentials | Bachelor's degree, often in life sciences; certifications like CCRP or GCP training | Bachelor's degree, relevant certifications often preferred |
| Work Environment | Global or multi-site clinical trials, often in international settings | Single-site or multi-site clinical trial management, primarily in hospitals or research centers |
| Employer & Industry Usage | Pharmaceutical companies, CROs, academic institutions involved in international studies | Hospitals, research institutions, pharmaceutical companies conducting clinical trials |
| Common Search & Comparison | Yes | Yes |
While both roles support clinical trial processes, the Associate International Clinical Research typically focuses on international or multi-site studies, requiring global coordination skills. The Clinical Research Coordinator usually manages local or site-specific trials, emphasizing patient interaction and trial administration. Understanding these differences helps candidates choose the role that best fits their experience and career goals.
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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.).Â
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.Â
- Support regional study feasibility, startup, and performance in partnership with regional partners.Â
- Provide regional clinical input into global development strategies, protocols, and study designs.Â
- 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.Â
- Demonstrated experience engaging with KOLs and investigators in ophthalmology and/or rare diseases across international regions.Â
- Strong understanding of GCP and global clinical development principles.Â
- 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 teamsÂ
- 30% travel
Education
Advanced degree in a scientific, medical, or health-related discipline
(PhD, PharmD, MD, or equivalent preferred).
Â
Generous. Innovative. Leadership-driven. Family-oriented. Socially responsible.Â
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.Â
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.Â
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.  Â
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.Â
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.
About Glaukos
Sourced by ZipRecruiter
Industry
Medical equipment and supplies manufacturing
Company size
51 - 200 Employees
Headquarters location
San Clemente, CA, US
Year founded
1998