1

Internship Global Study Associate Astrazeneca Jobs

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 ...

Establishes good collaboration with the Global Clinical Study Manager, Regional Clinical Trial Management Associates and other key stakeholders globally and regionally * Knowledgeable of clinical ...

next page

Showing results 1-20

Internship Global Study Associate Astrazeneca information

See salary details

$2.4K

$5.3K

$7.7K

How much do internship global study associate astrazeneca jobs pay per month?

As of Aug 8, 2026, the average monthly pay for internship global study associate astrazeneca in the United States is $5,290.17, according to ZipRecruiter salary data. Most workers in this role earn between $3,000.00 and $7,500.00 per month, depending on experience, location, and employer.

What is the difference between Internship Global Study Associate Astrazeneca vs Clinical Research Intern Astrazeneca?

AspectInternship Global Study Associate AstrazenecaClinical Research Intern Astrazeneca
Required CredentialsUndergraduate or graduate degree in life sciences or related fieldSimilar educational background, often pursuing related degrees
Work EnvironmentOffice-based, collaborative global teams, clinical trial supportOffice or lab setting, assisting clinical research activities
Employer & Industry UsageUsed in pharmaceutical and biotech companies, especially in clinical developmentCommon 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.

More about Internship Global Study Associate Astrazeneca jobs
What cities are hiring for Internship Global Study Associate Astrazeneca jobs? Cities with the most Internship Global Study Associate Astrazeneca job openings:
What states have the most Internship Global Study Associate Astrazeneca jobs? States with the most job openings for Internship Global Study Associate Astrazeneca jobs include:
Infographic showing various Internship Global Study Associate Astrazeneca job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 28% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $63,482 per year, or $30.5 per hour.

Associate Global Study Coordinator

Suvoda

Conshohocken, PA

Full-time

Posted 24 days ago


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. 

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.

#LI-CG1