The Associate Global Study Manager balances administrative coordination with hands-on, customer ... internships or entry-level project or study coordination work; * Proficiency with common business ...
The Associate Global Study Manager balances administrative coordination with hands-on, customer ... internships or entry-level project or study coordination work; * Proficiency with common business ...
The Associate Global Study Manager balances administrative coordination with hands-on, customer ... internships or entry-level project or study coordination work; * Proficiency with common business ...
The Associate Global Study Manager balances administrative coordination with hands-on, customer ... internships or entry-level project or study coordination work; * Proficiency with common business ...
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
Local Study Associate Director- FSP
Chesapeake, VA · On-site
$110 - $170/hr
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
New
Local Study Associate Director- FSP
Chesapeake, VA · On-site
$110 - $170/hr
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
New
Local Study Associate Director - FSP
$34.25 - $46.75/hr
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
Local Study Associate Director - FSP
$34.25 - $46.75/hr
Reports study progress/update to the Global Study Associate Director/ Global Study Team including Site Management and Monitoring (SMM) Lead. * Contributes to patient recruitment strategy including ...
Initiates, monitors, and closes study sites in compliance with AstraZeneca Procedural Documents ... Good cultural awareness and ability to work within global teams. * Proficiency with clinical ...
Initiates, monitors, and closes study sites in compliance with AstraZeneca Procedural Documents ... Good cultural awareness and ability to work within global teams. * Proficiency with clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Office based minimum 3 days per week AstraZeneca is a global, science-led, patient-focused ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Global Development Senior Medical Director, Hematology Oncology
Cambridge, MA · On-site
$288.06 - $432.09/hr
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Global Development Senior Medical Director, Hematology Oncology
Cambridge, MA · On-site
$288.06 - $432.09/hr
AstraZeneca is a global, science-led, patient-focused biopharmaceutical company that focuses on the ... Responsible for the ensuring the risk-benefit of a clinical study, ensuring that all clinical ...
Global Study Management Associate (gSMA)
$72K - $97K/yr
Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally * Knowledgeable of clinical ...
Global Study Management Associate (gSMA)
$72K - $97K/yr
Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally * Knowledgeable of clinical ...
Empowered to act on smart risks, you will translate strategy into decisive studies, accelerate ... Why AstraZeneca: Here, science and courage go hand-in-hand. You will work on one of the most ...
Empowered to act on smart risks, you will translate strategy into decisive studies, accelerate ... Why AstraZeneca: Here, science and courage go hand-in-hand. You will work on one of the most ...
Empowered to act on smart risks, you will translate strategy into decisive studies, accelerate ... Why AstraZeneca: Here, science and courage go hand-in-hand. You will work on one of the most ...
Empowered to act on smart risks, you will translate strategy into decisive studies, accelerate ... Why AstraZeneca: Here, science and courage go hand-in-hand. You will work on one of the most ...
Clinical Study Associate Manager
Armonk, NY · On-site
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
Clinical Study Associate Manager
Armonk, NY · On-site
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
Clinical Study Associate Manager
Warren, MI · On-site
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
Clinical Study Associate Manager
Warren, MI · On-site
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
We are seeking aClinical Study Associate Managerto join ourClinical Trial management team.In this ... with global study plans, and may contribute to global planning and management of the study
Internship Global Study Associate Astrazeneca information
See salary details
$2.4K - $2.9K
17% of jobs
$3K is the 25th percentile. Wages below this are outliers.
$2.9K - $3.4K
28% of jobs
$3.4K - $3.9K
3% of jobs
The median wage is $4K / yr.
$3.9K - $4.3K
5% of jobs
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$4.8K - $5.3K
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$6.7K - $7.2K
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$7.4K is the 75th percentile. Wages above this are outliers.
$7.2K - $7.7K
46% of jobs
$2.4K
$5.3K
$7.7K
How much do internship global study associate astrazeneca jobs pay per month?
What is the difference between Internship Global Study Associate Astrazeneca vs Clinical Research Intern Astrazeneca?
| Aspect | Internship Global Study Associate Astrazeneca | Clinical Research Intern Astrazeneca |
|---|---|---|
| Required Credentials | Undergraduate or graduate degree in life sciences or related field | Similar educational background, often pursuing related degrees |
| Work Environment | Office-based, collaborative global teams, clinical trial support | Office or lab setting, assisting clinical research activities |
| Employer & Industry Usage | Used in pharmaceutical and biotech companies, especially in clinical development | Common in clinical research departments within pharma companies |
The Internship Global Study Associate Astrazeneca and Clinical Research Intern Astrazeneca roles both target students or recent graduates in life sciences, with similar educational requirements and work environments. The main difference lies in the scope: the Study Associate focuses on supporting global clinical studies, while the Clinical Research Intern may assist with specific clinical trial tasks. Both roles serve as entry points into pharmaceutical clinical research careers.
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Job description
Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.
Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda's software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.
The Concierge team operates at the intersection of clinical trial operations and participant support, delivering travel and payment services across both the Concierge and Site Driven delivery models. The Study Management group serves as the operational backbone of clinical trial delivery, owning the full lifecycle of assigned studies from onboarding through closeout.Â
The Associate Global Study Manager balances administrative coordination with hands-on, customer-facing study support, acting as an extension of the Global Study Manager in maintaining accurate records, resolving day-to-day requests, and helping ensure studies stay compliant and on track.
Responsibilities:
Administrative Responsibilities
- Route incoming correspondence to the appropriate team member for action;
- Audit study documentation and shared files for accuracy and adherence to internal procedures;
- Prepare recurring internal and customer-facing reports;
- Assist in the maintenance of internally stored data;
- Support additional administrative and operational needs as assigned, which may include tracking participant transfers between studies, preparing expense-tracking materials, and coordinating region-specific documentation requirements;
Operational & Customer-Facing Responsibilities
- Create and maintain study playbooks that internal stakeholders use to stay aligned on study details, requirements, and expectations;
- Monitor and help resolve customer- and site-submitted requests for exceptions to standard study terms, escalating to the Global Study Manager as needed;
- Review coordinator-submitted activity on a recurring basis to catch and resolve discrepancies;
- Audit participant consent documentation on a quarterly basis;
- Monitor a shared safety-alert channel for events that could affect participant travel, escalating urgent matters promptly to the appropriate study team members;
- Serve as the customer-facing point of contact for a subset of studies requiring dedicated regional support, including coordinator onboarding and exception management for those studies;
- Act as a secondary point of contact after Global Study Manager for customer inquiries and day-to-day relationship management;
Qualifications:
- Bachelor's degree in Business, Healthcare Administration, Health Policy, or a related field preferred; equivalent experience considered;
- 1-3 years of post-graduate experience, including internships or entry-level project or study coordination work;
- Proficiency with common business and reporting software; ability to quickly learn internal systems and platforms;
- Strong written and oral communication skills, with good judgment about when and how to escalate customer- or participant-facing issues;
- High attention to detail, especially when auditing data or documentation for accuracy;
- Strong organizational skills; able to manage multiple recurring tasks and deadlines across a portfolio of studies;
- Discretion in handling sensitive information;
- Capable of working independently following training, with clearly defined escalation path to senior study management position;
- Comfortable operating across a range of digital tools - including Microsoft 365 and emerging AI-assisted technologies - with the adaptability to pick up new systems quickly;
- Strong interpersonal instincts - able to build trust with customers and participants alike, and to bring a human touch to what is often a sensitive, high-stakes experience.
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About Suvoda
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Conshohocken, PA, US
Year founded
2012