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Pfizer Clinical Study Manager Jobs (NOW HIRING)

Axogen

Clinical Study Manager

Tampa, FL

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the endtoend operational leadership of an Axogensponsored randomized controlled trial (RCT) and other ...

Global Channel Management, Inc.

$57/hr

Qualifications Clinical Study Manager needs 5 years relevant experience is required with a BSc, 3 years with a MS/MPH, or 2 years with PharmD/PhD/MD Clinical Study Manager requires: * Phase II/III ...

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 ...

Axogen

Clinical Study Manager

Tampa, FL · On-site

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the end-to-end operational leadership of an Axogen-sponsored randomized controlled trial (RCT) and other ...

Axogen

Clinical Study Manager

Tampa, FL · On-site

Job Summary of the Clinical Study Manager The Clinical Study Manager (CSM) is accountable for the end‑to‑end operational leadership of an Axogen‑sponsored randomized controlled trial (RCT) and ...

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 ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site +1

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

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 ...

Intuitive

Senior Clinical Study Manager

Sunnyvale, CA · On-site

This Lead Clinical Study Manager-4 (CSM IV) / Senior Clinical Study Manager role will develop and execute strategies for US and global first-human-use and pivotal pre-market clinical trials to help ...

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 ...

Veranex

Senior Clinical Study Manager

San Jose, CA · On-site

$125K - $179K/yr

The Senior Clinical Study Manager is responsible for planning, executing, and overseeing clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory ...

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 ...

Spyglass Pharma

Clinical Study Manager

Aliso Viejo, CA · On-site

$140K - $160K/yr

Summary: The Clinical Study Manager (CSM) plays a key role in the planning and execution of SpyGlass Pharma's clinical trials. Working closely with the Director of Clinical Research and cross ...

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 ...

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 ...

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All JobsPfizer Clinical Study Manager Jobs

Pfizer Clinical Study Manager information

See salary details

$22K

$125.3K

$206K

How much do pfizer clinical study manager jobs pay per year?

As of Jun 9, 2026, the average yearly pay for pfizer clinical study manager in the United States is $125,290.00, according to ZipRecruiter salary data. Most workers in this role earn between $85,000.00 and $157,000.00 per year, depending on experience, location, and employer.

What does a Pfizer Clinical Study Manager do?

A Pfizer Clinical Study Manager oversees the planning, execution, and completion of clinical trials for new drugs or treatments. They coordinate with cross-functional teams, ensure compliance with regulations, manage timelines and budgets, and maintain data integrity throughout the study. Their role is essential in ensuring that clinical studies are conducted efficiently and meet all scientific, ethical, and regulatory standards.

What are some of the main challenges a Pfizer Clinical Study Manager may face when overseeing global clinical trials?

As a Pfizer Clinical Study Manager, one of the main challenges is coordinating complex clinical trials across multiple countries and regulatory environments. This involves ensuring compliance with diverse local regulations, managing timelines, and adapting protocols to different healthcare settings. Additionally, effective communication with cross-functional teams, vendors, and investigators is crucial to address issues quickly and maintain study quality. Managing these logistical and regulatory complexities while maintaining data integrity and patient safety makes the role both challenging and rewarding.

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

To thrive as a Pfizer Clinical Study Manager, you need a solid background in life sciences or a related field, experience in clinical trial management, and knowledge of regulatory requirements such as GCP (Good Clinical Practice). Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and often a relevant certification like PMP or a clinical research credential is expected. Outstanding organizational skills, leadership, and effective communication enable collaboration across diverse teams and stakeholders. These competencies are vital to ensure studies are conducted efficiently, compliantly, and on schedule, supporting successful drug development outcomes.

What is the difference between Pfizer Clinical Study Manager vs Pfizer Clinical Research Associate?

AspectPfizer Clinical Study ManagerPfizer Clinical Research Associate
ResponsibilitiesOversees entire clinical trials, manages teams, ensures compliance, and coordinates study activities.Monitors clinical sites, collects data, and ensures protocol adherence at the site level.
Required CredentialsBachelor's or higher in life sciences, project management experience, and knowledge of GCP guidelines.Bachelor's in health sciences or related field, clinical monitoring experience, and GCP knowledge.
Work EnvironmentOffice-based with site visits, team management, and project coordination.Frequent site visits, monitoring activities, and data collection at clinical sites.

The Pfizer Clinical Study Manager typically oversees the entire clinical trial process, managing teams and ensuring compliance, while the Pfizer Clinical Research Associate focuses on monitoring clinical sites and collecting data. Both roles require similar educational backgrounds and GCP knowledge, but differ in scope and daily responsibilities.

Infographic showing various Pfizer Clinical Study Manager job openings in the United States as of May 2026, with employment types broken down into 100% Part Time. Highlights an 83% Physical, 3% Hybrid, and 14% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.
Clinical Study Manager

Clinical Study Manager

Global Channel Management, Inc.

New York, NY • On-site

$70/hr

Contractor

Posted 29 days ago

Job description

Company Description

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation.  Our account managers and recruiters have over a decade of experience in various verticals. GCM understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function.  Organizations need to reduce training and labor costs but at same requiring the best "talent " for the job. 


Qualifications

3-5 years
Strong Project Management
Regulatory submission experience
Oncology experience
Participate on a cross functional team focused on US regulatory submissions (FDA).
* Previous Pfizer experience is preferred; Pharmaceutical/biotech experience mandatory.
Familiarity with U.S. NDA processes required
Provides Financial Oversight
Forecasts and manages high level clinical trial budget. Oversees the study risk planning process (e.g. IQMP)
Works proactively with AP/CRO
Supports Practical Clinical Trial Design
o Partners with Clinician and other team members and supporting functional lines to provide operational expertise and insight to inform protocol design.
o Initiates and ensures a Protocol Operational Feasibility and Budget assessment is performed by seeking input from other lines within Development Operations and at the Alliance Partner/Vendor as needed.
o Facilitates early engagement of Alliance Partners/Vendors when needed.

Additional Information

$70/hr

6  months

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About Global Channel Management

Sourced by ZipRecruiter

Global Channel Management is a technology company that specializes in various types of recruiting and staff augmentation. Global Channel Management understands the challenges companies face when it comes to the skills and experience needed to fill the void of the day to day function. Organizations need to reduce training and labor costs but at the same time requiring the best talent for the job. GCM's Ownership and Management teams have extensive Staffing, Recruiting, HR and Executive Leadership knowledge, Experience and Expertise. Our Understanding and Commitment to our Client's Satisfaction are key reasons GCM has been successful in establishing long term relationships.

Industry

Recruiting and staffing services

Company size

11 - 50 Employees

Headquarters location

Austell, GA, US

Year founded

2009

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