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Clinical Project Manager Jobs in Encinitas, CA (NOW HIRING)

Project Manager

San Diego, CA ยท On-site

$130K - $160K/yr

Bachelor 's degree in Business Administration, Project Management, Healthcare Administration, Clinical Sciences, or a related field.Minimum of 10 years of experience managing complex projects.Active ...

Project Manager

San Diego, CA ยท On-site

$130K - $160K/yr

Bachelor 's degree in Business Administration, Project Management, Healthcare Administration, Clinical Sciences, or a related field.Minimum of 10 years of experience managing complex projects.Active ...

Project Manager

San Diego, CA ยท On-site

$130K - $160K/yr

Bachelor's degree in Business Administration, Project Management, Healthcare Administration, Clinical Sciences, or a related field. * Minimum of 10 years of experience managing complex projects.

Project Manager

San Diego, CA ยท On-site

$130K - $160K/yr

Bachelor's degree in Business Administration, Project Management, Healthcare Administration, Clinical Sciences, or a related field. * Minimum of 10 years of experience managing complex projects.

Project Manager

San Diego, CA ยท On-site

$100K - $225K/yr

PROJECT MANAGER Project Managers are responsible for onsite and off-site managing, directing, supervising and coordinating of the construction operations of high-end custom remodels and/or ground up ...

Project Manager

San Diego, CA ยท On-site

$100K - $225K/yr

PROJECT MANAGER Project Managers are responsible for onsite and off-site managing, directing, supervising and coordinating of the construction operations of high-end custom remodels and/or ground up ...

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Showing results 1-20

Clinical Project Manager information

See Encinitas, CA salary details

$31

$65

$116

How much do clinical project manager jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical project manager in Encinitas, CA is $65.20, according to ZipRecruiter salary data. Most workers in this role earn between $45.43 and $76.44 per hour, depending on experience, location, and employer.

What does a clinical project manager do?

A clinical project manager, or CPM, manages clinical trial studies for new drugs and medical devices. In this clinical management position, responsibilities and duties include working with all team members and all aspects of a clinical project, including subject selection and enrollment, record keeping, process auditing, and documentation. They also work with the budget and communicate with third parties, such as laboratories or investigators.

What does a clinical project manager do?

A Clinical Project Manager oversees the planning, execution, and completion of clinical trials in the pharmaceutical, biotechnology, or medical device industries. They coordinate teams, manage budgets, timelines, and ensure that studies comply with regulatory standards and company protocols. Clinical Project Managers act as the main point of contact between sponsors, vendors, and clinical research sites, working to ensure that trials progress smoothly and data integrity is maintained. Their role is critical in bringing new therapies and treatments to market safely and efficiently.

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

To thrive as a Clinical Project Manager, you need expertise in clinical trial management, regulatory compliance, and a relevant life sciences degree, often supported by experience in clinical research. Familiarity with project management tools, electronic data capture (EDC) systems, and certifications like PMP or ACRP are highly valued. Strong leadership, problem-solving, and communication skills help you effectively coordinate teams and stakeholders. These competencies ensure successful trial execution, regulatory adherence, and timely project delivery in a highly regulated environment.

What are some common challenges clinical project managers face when coordinating multi-site clinical trials?

Clinical Project Managers often encounter challenges such as maintaining consistent communication across different sites, ensuring adherence to regulatory guidelines, and managing timelines amidst unexpected delays. Coordinating multi-site trials requires balancing the needs of diverse teams, addressing site-specific issues, and ensuring data quality across all locations. Effective project management tools, regular status meetings, and proactive risk assessment are essential for overcoming these obstacles and keeping the study on track.

What is the difference between Clinical Project Manager vs Clinical Research Associate?

AspectClinical Project ManagerClinical Research Associate
CredentialsTypically requires a Bachelor's degree in life sciences, with many holding advanced degrees or certifications like PMPUsually holds a Bachelor's degree in life sciences or related field; certifications like CRA certification are common
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors and sitesMonitors clinical sites, ensures protocol compliance, and collects data
Employer & Industry UsageFound in pharmaceutical, biotech, and CRO companies overseeing entire projectsPrimarily employed by CROs and sponsors to monitor trial sites

The Clinical Project Manager and Clinical Research Associate roles are closely related but differ mainly in scope. The Clinical Project Manager oversees entire clinical trials, manages teams, and coordinates with stakeholders, while the Clinical Research Associate focuses on monitoring clinical sites and ensuring protocol adherence. Both roles require similar educational backgrounds and certifications, but their responsibilities and work environments differ significantly.

How much do clinical project managers earn?

Clinical project managers typically earn between $80,000 and $130,000 annually, depending on experience, location, and the size of the organization. Senior roles or those with specialized skills and certifications can earn higher salaries, often exceeding $150,000. Compensation may also include bonuses and benefits related to project scope and complexity.

What are popular job titles related to Clinical Project Manager jobs in Encinitas, CA?

For Clinical Project Manager jobs in Encinitas, CA, the most frequently searched job titles are:

What job categories do people searching Clinical Project Manager jobs in Encinitas, CA look for?

The top searched job categories for Clinical Project Manager jobs in Encinitas, CA are:

What cities near Encinitas, CA are hiring for Clinical Project Manager jobs?

Cities near Encinitas, CA with the most Clinical Project Manager job openings:

Infographic showing various Clinical Project Manager job openings in Encinitas, CA as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $135,616 per year, or $65.2 per hour.

Associate Clinical Project Manager / Clinical Project Manager

n-Lorem

San Diego, CA โ€ข On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 10 days ago


Job description

Description:

Reporting to: Senior Director, Clinical Operations and Project Management

Hours: Full-Time

Location: Onsite or Hybrid in San Diego, CA

Compensation: $80K-$100K


n-Lorem Foundation

Though n-Lorem is pioneering a novel non-profit model, to provide personalized experimental ASO treatments for free, for life to patients with the rarest of mutations (nano-rare), we are functionally a biotechnology company. We have a large and growing portfolio of ASO medicine discovery programs, ASO medicines in development and multiple clinical programs.

With a seasoned leadership team and strategic partnerships, the n-Lorem Foundation provides the framework, funds and access for nano-rare patients who are amenable to our technology to receive personalized ASO medicines for free, for life. We hope that you will consider joining us as we strive to change the world, one nano-rare patient at a time.

If you are a clinical project manager who champions organization, excellent communication (both written and verbal), efficiency and attention to detail. This role is well suited for someone who is motivated by purpose and impact, and who wants to contribute to a team united by the belief that we can change the world—one patient and one family at a time.


Job Overview

n-Lorem is seeking a passionate, organized, detail- and action-oriented individual to join our team as an Associate Project Manager or Project Manager. In this role, you will partner closely with the Senior Director of Clinical Operations and Project Management and the Vice President of Clinical Development. The successful candidate will help to manage n-Lorem’s portfolio of patients by working closely with a cross-functional team. You will be committed to excellent documentation, timeline management, process improvement, and efficiency. You will also ensure activities are streamlined within the organization based on rapidly evolving development and operational priorities. Your day-to-day activities will focus on the advancement of all n-Lorem Patient ASO programs and business operations activities to meet the needs of our patients and internal team. In general, you will assist the clinical operations and program management leadership teams with tasks such as ensuring consistent documentation across the n-Lorem portfolio, detailed record keeping of project details and communications, and working with a multi-disciplinary team to facilitate communication and forward progress of all patient programs. No two days will be the same and flexibility will be key as an important member of our fast-paced growing team.


Key Responsibilities:

  • Support the maintenance of centralized locations for all Clinical and Development Operations including dashboards, metrics reports, tools, and databases.
  • Work closely with Clinical Development and Program Management teams to track progress, manage timelines, document key decisions, maintain systems for organizing complex information, and respond to queries.
  • Proactively identify and address potential gaps across the organization to ensure patient programs run smoothly and stakeholders have access to business-critical information to enable decision making.
  • Meeting Planning, Management, and Follow-up, including:
- Scheduling.

- Facilitate group discussions with diverse perspectives across geographies, and bring teams to agreement.

- Development of tailored agendas to each unique patient program.

- Generate meeting minutes and track action items of varying scope and importance to ensure all items owned by you

(and others) are completed in a timely fashion.

  • Manage process to obtain and coordinate receipt of required data and materials for all patient programs.
  • Assist scientific teams with timeline tracking, and conduct periodic analyses of aggregate timeline data.
  • General document management including detailed record keeping and co-authoring process documents and standardized templates.
  • Creation and maintenance of critical external communication lists and team rosters.
  • Proactively identify inefficiencies and propose possible solutions and escalate potential issues.
  • Prepare reports and correspondence to investigators, partners, collaborators, and the n-Lorem leadership team.
  • Act as a liaison between internal n-Lorem teams and physician and institution teams.
  • Prioritize work in a fast-paced environment with evolving project priorities to meet deliverables and objectives.
  • Other duties as assigned to support our quickly-growing multi-disciplinary team.
Requirements:

Requirements:

  • U.S. work authorization.
  • Minimum of a Bachelor’s degree in a scientific or technical discipline.
  • 1-2+ years of experience in Project Management in the pharmaceutical or biotechnology industries.
  • Familiarity with the principles of clinical trial conduct including clinical drug development, clinical trials operations, and regulatory components.
  • Strong and crisp written and verbal communication with excellent customer service skills.
  • Ability to work effectively in a fast-paced, cross-functional environment with multiple stakeholders.
  • A team player who has a strong sense of ownership, accountability, and responsibility.
  • Strong attention to detail, organizational skills, and ability to manage multiple priorities.
  • Experience with Microsoft Office 365 and SharePoint.

n-Lorem offers a competitive benefits package including medical, dental, vision, 403(b), four weeks paid vacation, paid sick time, life insurance, employee assistance program. n-Lorem is a small foundation with an extraordinary mission, to provide hope and potentially help to nano-rare patients. Every employee in our organization is a significant contributor to this mission. We know that our work could have a profound impact on the life of a patient today.

n-Lorem is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status. n-Lorem is committed to providing reasonable accommodations for candidates with disabilities in our recruiting process. If you need any assistance or accommodations due to a disability, please let us know.


For more information on n-Lorem, please visit our website www.nlorem.org