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Pharmaceutical Project Manager Jobs in Riverside, CA

Stonhard

Be Seen First

Supervising Construction Manager

San Bernardino, CA · On-site

$90K - $110K/yr

Tracks, guies, and executes Total Project Management (TPM), including forecasting in a respective ... pharmaceutical, chemical processing, education, healthcare, government, technology and hospitality.

Crane Co.

Project Engineer

Jurupa Valley, CA · On-site

$80 - $100/hr

Time management** -- Ability to prioritize tasks and manage multiple projects.**Interpersonal ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · Hybrid

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

Crane Company

Project Engineer

Jurupa Valley, CA · On-site

$81K - $110K/yr

Time management - Ability to prioritize tasks and manage multiple projects. Interpersonal Skills ... Among the industries served are the chemical processing, biotechnology, pharmaceutical, oil & gas ...

AbbVie

Director, Portfolio Program Management

Irvine, CA · On-site

$160K/yr

Project manages the development of the deliverable team strategy across indications and ensures ... Bachelor of Science or Master of Science in Pharmaceutical Sciences or related field required * 8 ...

Guardian Pharmacy

Pharmacist

Anaheim, CA

$61 - $73.25/hr

Our core focus is delivering customized medication management solutions to support healthcare ... project teams to deadlines, while maintaining strong team orientation Relational - ability to build ...

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Pharmaceutical Project Manager information

See Riverside, CA salary details

$46.9K

$109.6K

$176.8K

How much do pharmaceutical project manager jobs pay per year?

As of Sep 7, 2026, the average yearly pay for pharmaceutical project manager in Riverside, CA is $109,570.00, according to ZipRecruiter salary data. Most workers in this role earn between $86,600.00 and $134,100.00 per year, depending on experience, location, and employer.

What is a pharmaceutical project manager?

A Pharmaceutical Project Manager oversees drug development projects from initiation to completion, ensuring they meet regulatory, budget, and timeline requirements. They coordinate cross-functional teams, including researchers, regulatory specialists, and manufacturing professionals, to bring pharmaceutical products to market. Their responsibilities include risk management, resource allocation, and stakeholder communication. Strong project management skills, industry knowledge, and attention to compliance are essential for success in this role.

What are the main challenges a pharmaceutical project manager faces during a drug development project?

Pharmaceutical Project Managers often encounter challenges such as navigating complex regulatory requirements, managing tight project timelines, and coordinating across multiple departments like clinical research, regulatory affairs, and manufacturing. Ensuring effective communication among diverse stakeholders and addressing unforeseen obstacles, such as changes in trial protocols or supply chain disruptions, are also common. Strong organizational and leadership skills are essential for adapting to evolving project demands and keeping teams aligned. By anticipating challenges and fostering collaboration, Pharmaceutical Project Managers help ensure successful project outcomes and regulatory approvals.

What are the key skills and qualifications needed to thrive as a pharmaceutical project manager, and why are they important?

A Pharmaceutical Project Manager needs a strong background in life sciences or pharmaceuticals, experience in project management, and often a relevant degree or certification such as PMP. Familiarity with tools like Microsoft Project, regulatory compliance systems (e.g., FDA or EMA guidelines), and document management platforms is crucial. Excellent communication, leadership, problem-solving, and organizational abilities set standout candidates apart. These skills are vital to effectively lead cross-functional teams, ensure regulatory compliance, and successfully deliver projects on time and within budget in a complex industry.

How much do pharmaceutical project managers make in the US?

Pharmaceutical project managers in the US typically earn between $90,000 and $130,000 annually, with salaries varying based on experience, location, and company size. Senior roles or those with specialized skills and certifications can earn higher compensation, often exceeding $150,000 per year.

How to become a pharmaceutical project manager?

To become a pharmaceutical project manager, candidates typically need a bachelor's degree in pharmacy, life sciences, or a related field, along with experience in pharmaceutical development or project coordination. Many roles require strong organizational, communication, and leadership skills, often supported by certifications such as PMP (Project Management Professional). Gaining industry-specific knowledge and experience with regulatory requirements can also enhance prospects in this field.

What are popular job titles related to Pharmaceutical Project Manager jobs in Riverside, CA?

For Pharmaceutical Project Manager jobs in Riverside, CA, the most frequently searched job titles are:

What job categories do people searching Pharmaceutical Project Manager jobs in Riverside, CA look for?

The top searched job categories for Pharmaceutical Project Manager jobs in Riverside, CA are:

What cities near Riverside, CA are hiring for Pharmaceutical Project Manager jobs?

Cities near Riverside, CA with the most Pharmaceutical Project Manager job openings:

Pharmaceutical Project Manager jobs near you
Infographic showing various Pharmaceutical Project Manager job openings in Riverside, CA as of August 2026, with employment types broken down into 83% Full Time, 15% Part Time, and 2% Contract. Highlights an 79% Physical, 2% Hybrid, and 19% Remote job distribution, with an average salary of $109,570 per year, or $52.7 per hour.

Manager, Aesthetics Clinical Development

AbbVie

Irvine, CA • On-site

$109K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 24 days ago

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 103 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.
Job Description
At Allergan Aesthetics, an AbbVie company, we develop, manufacture, and market a portfolio of leading aesthetics brands and products. Our aesthetics portfolio includes facial injectables, body contouring, plastics, skin care, and more.
With our own research and development team focused on driving innovation in aesthetics, we're committed to providing the most comprehensive science-based product offerings available.
To build all necessary data/information needed in preparing internal documents/scientific reports related to clinical trials and; to keep multiple reports moving forward simultaneously through multi-tasking.
  • Prepare scientific reports/presentations related to clinical trials using available software and templates and; review/contribute to clinical protocols, by utilizing expertise, to assist in interpretation of data.
  • Coordinate advisory meeting agendas, activities and slide decks and consulting agreements
  • Comply with procedures set forth in relevant IQS documents and Study protocols and other directives issued by the management regarding clinical studies.
  • Lead the study development by applying most current electronic document conventions/processes most consistently/accurately to ensure scientific integrity of all processes.
  • Responsible for receiving and completing tasks and assignments from function, Therapeutic Area MD or Scientific Staff within timeline with minimal supervision and; maximizing individual, function/therapeutic area and team productivity.
  • Participate on teams for process improvement initiatives and review key decisions impacting project timelines with management.
  • Apply experience to analyze clinical study data, including statistical data using available software to assist with ongoing blinded/un-blinded PK, safety and efficacy reviews and ensure the scientific integrity of all processes.
  • Perform literature/competitive intelligence searches to recognize/resolve scientific and technical problems by applying the most current electronic document conventions and processes consistently and accurately.
  • Provide/present key clinical study information to function/therapeutic area and management.
  • May lead teams within therapeutic area and supervise exempt and/or non-exempt direct reports and mentor function/-therapeutic area personnel.

The position is based onsite in Irvine, CA.
Qualifications
  • Bachelors/Master's degree, in Science related to Field with 11+ years' experience in the pharmaceutical industry or Pharm-D/PhD with 1+years
  • Ability to understand more complex clinical study principles
  • Advanced understanding of appropriate technology necessary to analyze clinical study data, generate reports and create presentations, posters and manuscripts
  • Experience in team, drug development, and scientific project leadership or related.
  • Experience supporting clinical research, drug development and/or function/therapeutic area operations.
  • Must have a proven record of successful projects.
  • Experience in multi-faceted, broad-based multiple functions/therapeutic areas or clinical functions with in depth knowledge of clinical study issues.
  • Ability to appropriately and effectively use resources to complete tasks and meet required timelines.
  • Ability to produce work of the highest quality by paying attention to detail
  • Must possess good oral and written communication skills

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.
  • This job is eligible to participate in our long-term incentive programs

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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