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Global Study Associate Astrazeneca Jobs (NOW HIRING)

AstraZeneca

Global Clinical Head

Boston, MA · On-site

$331K - $497K/yr

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here ... Delivered multiple complex and large studies (e.g., including but not limited to international ...

AstraZeneca

Global Clinical Head

Boston, MA · On-site

$331K - $497K/yr

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here ... Delivered multiple complex and large studies (e.g., including but not limited to international ...

AstraZeneca

Global Clinical Head

Boston, MA · On-site

$331K - $497K/yr

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here ... Delivered multiple complex and large studies (e.g., including but not limited to international ...

AstraZeneca

Global Clinical Head

Gaithersburg, MD

$331K - $497K/yr

At AstraZeneca, we put patients first and strive to meet their unmet needs worldwide. Working here ... Delivered multiple complex and large studies (e.g., including but not limited to international ...

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How much do global study associate astrazeneca jobs pay per hour?

As of Jun 25, 2026, the average hourly pay for global study associate astrazeneca in the United States is $39.99, according to ZipRecruiter salary data. Most workers in this role earn between $32.21 and $43.99 per hour, depending on experience, location, and employer.

What does a typical day look like for a Global Study Associate at AstraZeneca?

As a Global Study Associate at AstraZeneca, your typical day involves supporting global clinical study operations by maintaining study documentation, coordinating with internal teams and external vendors, and tracking study milestones. You'll often attend team meetings, update tracking systems, assist with regulatory submissions, and respond to queries from various stakeholders. The role requires close collaboration with clinical project managers, data managers, and other departments to ensure studies stay on schedule and adhere to compliance standards. This dynamic environment provides continuous learning and development opportunities.

What are the key skills and qualifications needed to thrive in the Global Study Associate Astrazeneca position, and why are they important?

To thrive as a Global Study Associate at AstraZeneca, you need a solid understanding of clinical research processes, attention to detail, and a relevant scientific degree. Familiarity with clinical trial management systems (CTMS), regulatory guidelines like ICH-GCP, and experience using tools such as Microsoft Office and electronic data capture platforms are important. Strong organizational, problem-solving, and communication skills help you navigate cross-functional teams and global projects effectively. These competencies ensure accurate study support, compliance, and seamless collaboration within complex, international research environments.

What is a Global Study Associate at AstraZeneca?

A Global Study Associate (GSA) at AstraZeneca supports the execution of clinical studies by coordinating administrative and operational tasks. This role involves collaborating with cross-functional teams, maintaining study documentation, and ensuring compliance with regulatory requirements. GSAs assist in study planning, tracking progress, and managing logistics to help deliver high-quality clinical trials. They play a crucial role in ensuring studies run smoothly and meet company and regulatory standards.

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Infographic showing various Global Study Associate Astrazeneca job openings in the United States as of June 2026, with employment types broken down into 90% Full Time, 1% Temporary, 8% Contract, and 1% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $83,169 per year, or $40 per hour.

Sr Clinical Study Assoc CO

Daiichi Sankyo, Inc.

Basking Ridge, NJ • On-site

$100K - $151K/yr

Other

Posted 21 days ago

Job description

At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.

Job Summary Assist in planning and execution of clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food and Drug Administration (FDA) regulations/EU Directive, and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP). Job Description Responsibilities Reconcile the TMF document trackers generated by the CRO with the document archive.

Bring issues with the reconciliation to the attention of the Study Manager and propose remediation plan. Distribute key study documents to the CRO and vendors as appropriate. Provide clinical administrative support to the study teams.

This may include preparing meeting logistics, distributing agendas, and minutes for study team meeting, meetings with Academic Research Organizations (AROs), and meetings with CRO and Investigator Meetings. Support Fair Market Value process in evaluating study budgets Collect information and coordinate with DS Regulatory Operations to post trial information on required public forums (eg.clinicaltrials.gov). Under supervision, review and document CRO-generated reports, such as site monitoring trip reports and protocol deviation reports and elevate issues to the attention of the supervisor.

Compile and maintain a monitoring review spreadsheet. Compile and maintain CRO Oversight Monitoring (CROOM) visit output Analyze study site metrics reports to identify potential areas of concern and bring to supervisor’s attention. Track study metrics such as site start-up, Investigator/site performance, recruitment, regulatory documents, TMF filing and QC activities and elevate areas of concern to your supervisor.

Create/maintain spreadsheets to track other items as needed, (e.g. Vendor invoices). Works with Insurance Brokers to obtain study site Insurance Provide tracking and oversight to the Vendor handling lab logistics and any other vendors deemed appropriate.

Participate in training; make recommendations for areas of improvement and innovation (study, or departmental level). Work with supervisor to provide input into individual career development plan. Responsibilities Continued Qualifications Education Qualifications Bachelor's Degree (preferred in Life Sciences) with relevant clinical development experience required Experience Qualifications 2 or more years work experience with Bachelors degree required Experience considered relevant includes clinical or basic research in a Pharmaceutical company, a Medical device/Diagnostic company, Academic Research Organization (ARO) or Contract Research Organization (CRO).

CRA experience preferred Time spent directly in a medical environment (e.g. as a Study Site Coordinator) is also considered relevant. preferred Travel Requirements Ability to travel up to 5% of the time.

In-house office position that may require occasional travel. Additional Information Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer.

Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law. Salary Range: USD$100,960.00 - USD$151,440.00 Download Our Benefits Summary PDF

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