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Clinical Project Associate Jobs (NOW HIRING)

Clinical Research Associate (CRA) certification or equivalent certification in project management is desired. * Working knowledge of Good Clinical Practice (GCP) / Good Study Practice (GSP) as ...

Clinical Research Associate (CRA) certification or equivalent certification in project management is desired. * Working knowledge of Good Clinical Practice (GCP) / Good Study Practice (GSP) as ...

Clinical Research Associate (CRA) certification or equivalent certification in project management is desired. * Working knowledge of Good Clinical Practice (GCP) / Good Study Practice (GSP) as ...

Clinical Research Associate (CRA) certification or equivalent certification in project management is desired. * Working knowledge of Good Clinical Practice (GCP) / Good Study Practice (GSP) as ...

Clinical Research Associate (CRA) certification or equivalent certification in project management is desired. * Working knowledge of Good Clinical Practice (GCP) / Good Study Practice (GSP) as ...

Project Associate

Baltimore, MD · On-site

$75K - $80K/yr

Project Associate Location: Baltimore, MD Salary: $65k - $85k About Pharmaron Pharmaron is a global ... and 1,000+ clinical trials across all phases. Our teams are involved in everything from small ...

Project Associate

Baltimore, MD · On-site

$65K - $85K/yr

Project Associate Location: Baltimore, MD Salary: $65k - $85k About Pharmaron Pharmaron is a global ... and 1,000+ clinical trials across all phases. Our teams are involved in everything from small ...

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Clinical Project Associate information

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$12

$31

$55

How much do clinical project associate jobs pay per hour?

As of May 30, 2026, the average hourly pay for clinical project associate in the United States is $31.54, according to ZipRecruiter salary data. Most workers in this role earn between $21.15 and $41.59 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?

To thrive as a Clinical Project Associate, you need a background in life sciences or a related field, attention to detail, and strong organizational skills. Familiarity with clinical trial management systems (CTMS), regulatory documentation, and tools like Microsoft Office is typically required. Excellent communication, teamwork, and time management abilities help professionals excel in supporting project coordination. These skills are crucial for ensuring regulatory compliance, smooth project execution, and effective collaboration within clinical research teams.

What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?

As a Clinical Project Associate, you will play a vital role in ensuring the smooth execution of clinical trials by handling administrative and logistical tasks. Your responsibilities often include maintaining study documentation, coordinating meetings, tracking project timelines, and supporting communication between internal teams and external partners such as clinical sites and vendors. You may also assist with regulatory submissions and help monitor compliance with study protocols. This position offers excellent exposure to the clinical research process and can be a stepping stone to more advanced roles within clinical operations.

What is a Clinical Project Associate?

A Clinical Project Associate (CPA) is a professional who supports the planning, execution, and management of clinical trials in the pharmaceutical, biotechnology, or medical device industries. Their responsibilities often include coordinating study documentation, assisting with regulatory submissions, tracking project timelines, and facilitating communication among study teams. CPAs play a crucial role in ensuring that clinical trials are conducted efficiently, ethically, and in compliance with regulatory standards. They work closely with clinical project managers, research associates, and other team members to help bring new therapies and treatments to market.

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

AspectClinical Project AssociateClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree in health or related field; certifications like CCRP common
Work EnvironmentTypically works with project teams, sponsors, and CROs in clinical trial settingsWorks directly with patients, investigators, and site staff at clinical trial sites
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, clinics, research sites
Search & Comparison IntentHigh overlap in responsibilities and certificationsSimilar roles but more patient-facing

The Clinical Project Associate primarily supports clinical trial management from a project perspective, working with sponsors and CROs. In contrast, the Clinical Research Coordinator focuses on patient interactions and site management. Both roles require similar educational backgrounds and certifications, but their work environments and daily tasks differ significantly.

More about Clinical Project Associate jobs
What cities are hiring for Clinical Project Associate jobs? Cities with the most Clinical Project Associate 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 Associate jobs? States with the most job openings for Clinical Project Associate jobs include:
Infographic showing various Clinical Project Associate job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 72% Full Time, 19% Part Time, 1% Temporary, and 7% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $65,604 per year, or $31.5 per hour.

Other

Posted 26 days ago


Job description

Foster City, CA
Contract Duration: 6-24 months
Rate: Negotiable
Salary: NA $1.00
Responsibilities:

  • Excellent employment opportunity for a Clinical Project Associate in the Foster City, CA area.
  • Work under general supervision for routine tasks and with detailed instructions on new assignments.
  • Tracking and preparing study-specific information utilizing databases, spreadsheets, and other tools.
  • Processes drug shipments, drug returns, and assists with in-house drug reconciliation.
  • Orders and maintains inventory of clinical supplies.
  • Orders and ships case report forms.
  • Assists with development of documents for site binders.
  • Assembles and prepares distribution of site binders.
  • Serves as CRA back up providing verbal and written communication with study personnel.
  • Under close supervision reviews and participates in the quality assurance of data or documents.
  • Arranges meeting logistics.
  • Drafts meeting agendas and assists in preparing meeting minutes.
  • May assist with monitoring visits under the direct supervision of senior staff.
  • Travel may be required.
Experience:
  • BA is a requirement
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • Must be familiar with Word, PowerPoint, and Excel.
  • Knowledge of FDA and or EMEA Regulations, ICH Guidelines, GCPs, and/or familiarity with standard clinical operating procedures is a plus.
  • Must be able to work both independently and as part of a team.
  • Has experience with managing paper and electronic TMF studies.