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Study Manager Jobs (NOW HIRING)

AstraZeneca

Global Study Manager

South San Francisco, CA · On-site

$112K - $168K/yr

Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a ...

AstraZeneca

Global Study Manager

South San Francisco, CA · On-site

$112K - $168K/yr

Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a ...

AstraZeneca

Global Study Manager

Gaithersburg, MD · On-site

$112K - $168K/yr

Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a ...

AstraZeneca

Global Study Manager

Gaithersburg, MD · On-site

$112K - $168K/yr

Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a ...

AstraZeneca

Global Study Manager

South San Francisco, CA

$112K - $168K/yr

Join us as aGlobal Study Manager in Cell Therapy, where you willbe responsible forsupporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a high ...

Danaher

Senior Clinical Study Manager

The Senior Clinical Study Manager is responsible for clinical trial execution within the US and EU regions for Leica Biosystems. This role will specifically support Leica Biosystems, an operating ...

ICON

Global Study Manager

Blue Bell, PA · On-site +1

Global Study Manager - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Icon plc

Global Study Manager

Blue Bell, PA · On-site +1

Global Study Manager - Oncology - Home Based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

Philips

Clinical Study Manager

$114K - $182K/yr

Job Title Clinical Study Manager Clinical Study Manager The Clinical Study Manager for Sleep & Respiratory Care oversees the execution and regulatory compliance of clinical studies, managing ...

ARTHREX

Clinical Study Manager

Naples, FL

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Clinical ...

Philips

Clinical Study Manager

Seattle, WA · On-site

$114K - $182K/yr

Clinical Study Manager The Clinical Study Manager for Sleep & Respiratory Care oversees the execution and regulatory compliance of clinical studies, managing documentation, negotiations, and team ...

New

ARTIDIS

Clinical Study Manager

Houston, TX · On-site

The Clinical Study Manager is an integral part of the Clinical Operations Team which manages planned and ongoing clinical studies. The Clinical Study Manager is responsible for overseeing the ...

Mobia Medical, Inc.

Clinical Study Manager

Fridley, MN · On-site

$110K - $160K/yr

About the role The Clinical Study Manager is a key member of the Clinical Affairs team, responsible for leading the operational execution and management of clinical studies that support the company ...

TEEMA

Study Manager - Mining & Metals

Phoenix, AZ · On-site

$90K - $145K/yr

Study Manager - Mining & Metals (PFS / FS) Location: Phoenix, AZ (Onsite) Role Type: Direct Hire | Senior Leadership The Opportunity Are you a strategic engineer who thrives in the Front-End of ...

Cordis

Clinical Study Manager

Irvine, CA · On-site +1

$114K - $165K/yr

Responsibilities The Clinical Study Manager (CSM) is responsible for the operational management and execution of clinical trials, ensuring studies are delivered on time, within budget, and in ...

Penumbra

Clinical Study Manager

General Summary The Clinical Study Manager provides leadership in the planning, design, and execution of clinical studies sponsored by Penumbra to assess safety and effectiveness of products. This ...

Arthrex

Clinical Study Manager

Naples, FL · On-site

Clinical Study Manager Arthrex, Inc. is a global medical device company and a leader in new product development and medical education in orthopedics. Arthrex is actively searching for a Clinical ...

Danaher

Senior Clinical Study Manager

Chaska, MN · On-site

$135K/yr

The Senior Clinical Study Manager is responsible for managing clinical trial execution from feasibility assessments through study closeout. This position reports to the Senior Manager Clinical ...

Intuitive

Sr. Clinical Study Manager

Sunnyvale, CA · On-site +1

The Clinical Study Manager-4 (CSM IV) role will develop and execute strategies for clinical and outcomes research studies to help regulatory approvals and key strategic evidence initiatives. As a ...

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Study Manager information

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$24.5K

$59.5K

$116K

How much do study manager jobs pay per year?

As of Jun 25, 2026, the average yearly pay for study manager in the United States is $59,525.00, according to ZipRecruiter salary data. Most workers in this role earn between $42,000.00 and $68,500.00 per year, depending on experience, location, and employer.

How does a Study Manager typically collaborate with cross-functional teams during the course of a clinical trial?

As a Study Manager, you'll work closely with cross-functional teams including clinical research associates, data managers, regulatory affairs, and biostatisticians to ensure the trial progresses smoothly and meets regulatory requirements. Regular meetings, status updates, and shared project management tools facilitate clear communication and timely issue resolution. You will often serve as the central point of contact, coordinating tasks and resolving conflicts between departments to keep the study on track. Collaboration skills are essential, as you’ll need to balance input from multiple stakeholders while maintaining study timelines and quality standards.

What are the key skills and qualifications needed to thrive as a Study Manager, and why are they important?

To thrive as a Study Manager, you need a solid background in clinical research, regulatory compliance, and project management, often supported by a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and GCP certification is typically required. Strong organizational skills, attention to detail, and effective communication are essential soft skills for coordinating teams and stakeholders. These qualifications ensure the successful planning, execution, and oversight of clinical studies within regulatory and timeline requirements.

What jobs pay $10,000 a month without a degree?

A Study Manager typically earns less than $10,000 monthly without a degree, but some high-paying roles like sales managers, real estate brokers, or skilled trades such as electricians and plumbers can reach or exceed this income level through experience and commissions. These jobs often require specialized skills, certifications, or extensive experience rather than formal degrees.

What does a Study Manager do?

A Study Manager is responsible for overseeing the planning, execution, and completion of research studies, often in clinical or academic settings. They coordinate between various stakeholders, including research teams, sponsors, and regulatory authorities, to ensure studies are conducted efficiently and in compliance with relevant guidelines. Study Managers manage timelines, budgets, and resources, while also handling documentation and reporting requirements. Their role is critical to ensuring that studies meet their scientific objectives and adhere to ethical standards.

What is the role of a study manager?

A study manager oversees the planning, execution, and monitoring of clinical or research studies to ensure they are completed on time, within scope, and according to regulatory standards. They coordinate with teams, manage budgets, and ensure compliance with protocols and Good Clinical Practice (GCP) guidelines.

Can you be a CRA with no experience?

A Clinical Research Associate (CRA) typically requires prior experience in clinical trials, monitoring, or related healthcare fields. Entry-level CRA positions may be available for candidates with strong organizational skills and relevant certifications, but most employers prefer candidates with some industry experience or training in Good Clinical Practice (GCP).

What jobs pay 2000 a day?

High-paying jobs that can pay around $2,000 a day typically include specialized roles such as senior corporate consultants, experienced surgeons, high-level executives, or successful entrepreneurs. These positions often require advanced skills, extensive experience, and sometimes certifications or licenses, and may involve consulting, project management, or leadership responsibilities.
More about Study Manager jobs
What cities are hiring for Study Manager jobs? Cities with the most Study Manager job openings:
What are the most commonly searched types of Study jobs? The most popular types of Study jobs are:
What states have the most Study Manager jobs? States with the most job openings for Study Manager jobs include:
Study Manager jobs near you
Infographic showing various Study Manager job openings in the United States as of June 2026, with employment types broken down into 50% Full Time, 46% Part Time, and 4% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $59,525 per year, or $28.6 per hour.
Global Study Manager

Global Study Manager

AstraZeneca

South San Francisco, CA • On-site

$112K - $168K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 25 days ago

AstraZeneca rating

8.6

Company rating: 8.6 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

16th of 72 rated pharmaceutical

Job description

Are you ready to make a bold move in your career? Join us as a Global Study Manager in Cell Therapy, where you will be responsible for supporting the delivery of cell therapy clinical studies ensuring quality and compliance. This role requires a high degree of flexibility as the exact accountabilities will differ depending on the nature of the clinical program or study.
As a Global Study Manager, you will contribute to the development of study documents, lead the preparation of country-specific agreements, manage third-party vendors, provide input to data management documents, and ensure the supply of study materials. You will also oversee third-party vendors, global / local internal staff, and investigator sites to support effective delivery of a study. Your role will involve monitoring study conduct and progress, support risk management and quality efforts, and assisting in the implementation of audits and regulatory inspections. You will be based in Gaithersburg, MD and will report to the Director, Study Management Cell Therapy.
Essential Qualifications:
  • Bachelor's degree with 4+ years of experience as a study manager
  • Experience of working with and delivering through strategic partners and 3rd party vendors
  • Excellent knowledge of ICH-GCP principles
  • Ability to lead, coordinate and prioritize multiple tasks and deliverables
  • Vendor Management experience
  • Proactive approach to achieving study goals
  • Demonstrated verbal and written communication skills
  • Good negotiation and collaboration skills
  • Demonstrated interpersonal and problem-solving skills
  • Ability to manage change with a high degree of flexibility
  • Some travel may be required

Desirable Experience:
  • Early/late phase oncology clinical trial experience
  • Experience in autologous or allogeneic therapies
  • Clinical Study Management experience

#CellTherapy
The annual base pay for this position ranges from $112K to $168K. Our positions offer eligibility for various incentives-an opportunity to receive short-term incentive bonuses, equity-based awards for salaried roles and commissions for sales roles. Benefits offered include qualified retirement programs, paid time off (i.e., vacation, holiday, and leaves), as well as health, dental, and vision coverage in accordance with the terms of the applicable plans.
At AstraZeneca, we follow the science and pioneer new frontiers. Our Oncology R&D team is dedicated to eliminating cancer as a cause of death. It's our big vision that unites and inspires us. With multiple indications and high-quality molecules at all stages of our innovative pipeline, we keep pushing forward. Fusing cutting-edge science with the latest technology to achieve breakthroughs. We are pioneers of collaborative research and have built an unrivalled scientific community both internally and externally. Working seamlessly and inclusively together we expedite research in some of the hardest-to-treat cancers. You can have the opportunity to build a rewarding and meaningful career as part of the team committed to improving the lives of millions with cancer.
Ready to make a difference? Apply now and join us in our mission to eliminate cancer as a cause of death!
Why AstraZeneca?
At AstraZeneca when we see an opportunity for change, we seize it and make it happen, because any opportunity no matter how small, can be the start of something big. Delivering life-changing medicines is about being entrepreneurial - finding those moments and recognizing their potential. Join us on our journey of building a new kind of organization to reset expectations of what a bio-pharmaceutical company can be. This means we're opening new ways to work, pioneering innovative methods and bringing unexpected teams together. Interested? Come and join our journey.
Date Posted
01-Jun-2026
Closing Date
28-Jun-2026
Our mission is to build an inclusive environment where equal employment opportunities are available to all applicants and employees. In furtherance of that mission, we welcome and consider applications from all qualified candidates, regardless of their protected characteristics. If you have a disability or special need that requires accommodation, please complete the corresponding section in the application form.

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