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Clinical Project Assistant Jobs (NOW HIRING)

At least 1 year of experience in a Clinical Project Specialist, Clinical Trial Assistant, Clinical Trial Coordinator, Project Coordinator, or comparable clinical operations support role is strongly ...

At least 1 year of experience in a Clinical Project Specialist, Clinical Trial Assistant, Clinical Trial Coordinator, Project Coordinator, or comparable clinical operations support role is strongly ...

At least 1 year of experience in a Clinical Project Specialist, Clinical Trial Assistant, Clinical Trial Coordinator, Project Coordinator, or comparable clinical operations support role is strongly ...

The PM works with the various departments throughout Emerus to assist in the successful completion ... Lead enterprise-wide projects including clinical programs, operational improvements, and capital ...

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Clinical Project Assistant information

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How much do clinical project assistant jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for clinical project assistant in the United States is $20.23, according to ZipRecruiter salary data. Most workers in this role earn between $16.59 and $23.32 per hour, depending on experience, location, and employer.

What is a clinical project assistant?

Clinical Project Assistants are support professionals who help manage and coordinate activities within clinical research projects. They assist project managers and clinical teams by handling administrative tasks, organizing documentation, scheduling meetings, and ensuring regulatory compliance. Their role is essential for keeping clinical trials running smoothly, maintaining accurate records, and facilitating communication among team members. Clinical Project Assistants often work in pharmaceutical companies, contract research organizations, or healthcare settings.

What are the key skills and qualifications needed to thrive as a clinical project assistant?

To thrive as a Clinical Project Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and regulatory documentation processes is typically required. Excellent communication, teamwork, and time management skills help you coordinate effectively with diverse stakeholders. These competencies are crucial for maintaining accurate trial documentation, ensuring regulatory compliance, and supporting efficient clinical study operations.

What are some common challenges faced by clinical project assistants, and how can they be managed effectively?

Clinical Project Assistants often encounter challenges such as managing multiple tasks across different projects, maintaining accurate and timely documentation, and ensuring effective communication among cross-functional teams. To manage these effectively, it's important to develop strong organizational and prioritization skills, utilize project management tools, and regularly communicate with project managers and team members to stay aligned on timelines and expectations. Proactive problem-solving and attention to detail can also help prevent issues and contribute to the smooth progress of clinical trials.

What is the difference between Clinical Project Assistant vs Clinical Research Coordinator?

AspectClinical Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree; some roles prefer certification or experience
Work EnvironmentSupports project teams in clinical trial settings, often within pharmaceutical or biotech companiesManages and oversees clinical trials at research sites or hospitals
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic research centers, clinical trial sites
Search & Comparison IntentHigh overlap in job duties and required skills, often searched together

The Clinical Project Assistant primarily supports clinical trial projects by assisting with documentation, scheduling, and communication within the project team. In contrast, the Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites, including patient recruitment and data collection. While both roles require similar educational backgrounds and work in related environments, their responsibilities differ in scope and focus.

What cities are hiring for Clinical Project Assistant jobs?

Cities with the most Clinical Project Assistant job openings:

What are the most commonly searched types of Clinical Project jobs?

The most popular types of Clinical Project jobs are:

What states have the most Clinical Project Assistant jobs?

States with the most job openings for Clinical Project Assistant jobs include:

What are popular job titles related to Clinical Project Assistant jobs?

For Clinical Project Assistant jobs, the most frequently searched job titles are:

Infographic showing various Clinical Project Assistant job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $42,079 per year, or $20.2 per hour.

Associate Clinical Project Manager / Clinical Project Manager

San Diego, CA • On-site

$80K - $100K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 2 days ago


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, and respond to queries.

  • Manage process to obtain and coordinate receipt of required data and materials for all patient programs.


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