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Pfizer Clinical Study Manager Jobs (NOW HIRING)

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 ...

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 ...

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 ...

Pfizer

Manager, Clinical Pharmacology

Bothell, WA

$106K - $176K/yr

Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Pfizer

Manager, Clinical Pharmacology

La Jolla, CA · On-site

$106K - $176K/yr

Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Pfizer

Manager, Clinical Pharmacology

Groton, CT

$106K - $176K/yr

Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Pfizer

Manager, Clinical Pharmacology

San Diego, CA · On-site

$106K - $176K/yr

Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

Pfizer

Manager, Clinical Pharmacology

Cambridge, MA

$106K - $176K/yr

Provides the clinical pharmacology components to Clinical Study Protocols, Clinical Study Reports ... Pfizer compensation structures and benefit packages are aligned based on the location of hire. The ...

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Pfizer Clinical Study Manager information

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$22K

$125.3K

$206K

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

As of Jun 16, 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 June 2026, with employment types broken down into 100% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $125,290 per year, or $60.2 per hour.

Clinical Study Manager, Clinical Operations

Daiichi Sankyo, Inc.

Basking Ridge, NJ • On-site

Full-time

Posted 21 days ago

Job description

Job Title: Clinical Study Manager, Clinical Operations
Job Requisition ID: 1536
Posting Start Date: 5/26/26
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
The Clinical Study Manager is responsible for the delivery and execution of global clinical studies under the direction of a Study Delivery Lead. This role is primarily focused on tactical study delivery and reports to a Director or higher-level position. The position requires excellent written and verbal communication, project management skills, and attention to detail. The Clinical Study Manager will have routine interaction with key internal and external stakeholders to communicate project status, resolve issues, and troubleshoot routine inquiries. This position may require the Clinical Study Manager to take on a dual role of both operational strategy and study execution.
Job Description
Responsibilities
Clinical Operations Study Management(Global) has primary accountability for operational execution and delivery of assigned clinical trials, including study level time, cost and quality deliverables. In a CRO outsourcing model, responsibilities also include:
  • Study Oversight: Lead the clinical study operational aspects of planning, execution, and management of one or more Phase 1-3 clinical trials. May provide support as back-up to the Study Delivery Lead as needed.
  • Cross-Functional Leadership: Participate and provide expertise as a cross-functional study team member, including vendors, and liaise with other departments. Provide mentorship of more junior Operations team members.
  • Vendor Management: Lead vendor selection, contracting, and management to maintain study quality and compliance and adherence to scope of work within timelines and budget. Oversee complex vendors (i.e., eCOA).
  • CRO Oversight: Responsible for the oversight, performance, and management of CRO(s) and 3rd party vendors (sub-contracted by CRO) to ensure compliance with Daiichi Sankyo's quality measures and adherence to scope of work within timelines and budget at a task level. Coordinate and develop materials for CRO KOMs and Investigator meetings.
  • Compliance and Regulatory: Ensure compliance with GCP/ICH guidelines and other regulatory requirements (FDA, MHRA, etc.).
  • Timeline and Budget Management: Create and coordinate clinical study timelines and budgets with Global Project Management and R&D Finance to meet critical milestones and manage budgets. Responsible for continual review of study timelines and study budget.
  • Risk Management: Identify, mitigate, and escalate risks per process throughout the study lifecycle. Ensure risks are appropriately logged in the risk management system.
  • Study Material Development: Co-develop and manage study materials, including training materials, protocols, CRFs, and study operational plans. Ensure all necessary operational materials are in place.
  • Data Cleaning: Oversee site and monitor data cleaning metrics including EDC data entry, query resolution timeliness, and protocol deviation review.
  • Site Management: Oversee site selection, start-up, monitoring, and closeout for the trial.
  • Study Communication: Triage, resolve or escalate study issues /risk mitigations to the Study Delivery Lead.
  • Support all inspection readiness and quality initiatives pertaining to assigned stud(ies).).
    o Supports risk Management initiatives
    o Supports audit/inspection activities as needed
    o Ensures trial master file is complete and accurate for assigned stud(ies)
  • Communication and Reporting: Provide regular updates on study progress to key stakeholders.
  • Training: Identify training needs for key stakeholders as needed, e.g., study team members, vendors and ensure training is carried out. Develop training materials as necessary.

Responsibilities Continued
Qualifications
Education Qualifications
Bachelor's Degree preferred in Life Sciences required
Experience Qualifications
3 or more years required and
Relevant experience is required with a BSc required and
Experience in oversight of global clinical trials (all phases) in all stages of delivery with requisite industry training and experience required and
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). preferred
CRA experience preferred
Time spent directly in a medical environment (e.g. as a Study Site Coordinator) preferred
Familiarity to a Japan-based organization preferred
Travel Requirements
Ability to travel up to 10% of the time. In-house office position that may require occasional travel (domestic or global).
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$136,080.00 - USD$204,120.00
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