Clinical Project Associate
Parsippany, NJ · On-site
An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong ...
Clinical Project Associate
Parsippany, NJ · On-site
An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong ...
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
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Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
New
Clinical Project Associate
Madison, NJ · On-site +1
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
Clinical Project Associate
Madison, NJ · On-site +1
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
Title: Clinical Project Associate Duration: 06 Months Location: Foster City, CA Job Responsibilities & Skills * Project involvement will be in an administrative role. * Provides administrative ...
Title: Clinical Project Associate Duration: 06 Months Location: Foster City, CA Job Responsibilities & Skills * Project involvement will be in an administrative role. * Provides administrative ...
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
New
Quick apply
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
New
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
New
Quick apply
Position Summary The Clinical Project Associate (CPA) is responsible for working with research sites and the clinical research team to facilitate the successful and timely conduct of clinical ...
New
Clinical Project Associate
$61K - $87K/yr
As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH ...
Clinical Project Associate
$61K - $87K/yr
As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH ...
Clinical Project Associate
Cambridge, MA · On-site
$61K - $87K/yr
As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH ...
Clinical Project Associate
Cambridge, MA · On-site
$61K - $87K/yr
As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH ...
Clinical Project Associate
Foster City, CA · On-site
$39 - $53.25/hr
Project involvement will be in an administrative role. Provides administrative support to the ... Clinical Operations function including set-up, maintenance and reconciliation of the Trial Master ...
Clinical Project Associate
Foster City, CA · On-site
$39 - $53.25/hr
Project involvement will be in an administrative role. Provides administrative support to the ... Clinical Operations function including set-up, maintenance and reconciliation of the Trial Master ...
Clinical Project Associate
$39 - $53.25/hr
Project involvement will be in an administrative role. Provides administrative support to the ... Clinical Operations function including set-up, maintenance and reconciliation of the Trial Master ...
Clinical Project Associate
$39 - $53.25/hr
Project involvement will be in an administrative role. Provides administrative support to the ... Clinical Operations function including set-up, maintenance and reconciliation of the Trial Master ...
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.
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.
Must meet all requirements for CPA grade 24 position and have demonstrated proficiency in all relevant areas Provide input and assist with harmonization of Clinical Operations databases and tracking ...
Must meet all requirements for CPA grade 24 position and have demonstrated proficiency in all relevant areas Provide input and assist with harmonization of Clinical Operations databases and tracking ...
Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures * Must be familiar with Word, PowerPoint, and Excel * Excellent verbal and ...
Knowledge of FDA and EMA Regulations, ICH Guidelines, GCP, and familiarity with standard clinical operating procedures * Must be familiar with Word, PowerPoint, and Excel * Excellent verbal and ...
Provide input and assist with harmonization of Clinical Operations databases and tracking tools. * Assist in the maintaining clinical information and training of Clinical Operations personnel in the ...
Provide input and assist with harmonization of Clinical Operations databases and tracking tools. * Assist in the maintaining clinical information and training of Clinical Operations personnel in the ...
Clinical Project Associate - Remote US
Concord, NC · Remote
$31.25 - $42.50/hr
As the Clinical Project Associate , you are responsiblefor ensuring the Trial Master File (TMF) is set-up and maintained in "audit ready" condition; and conduct critical documentation collection and ...
New
Clinical Project Associate - Remote US
Concord, NC · Remote
$31.25 - $42.50/hr
As the Clinical Project Associate , you are responsiblefor ensuring the Trial Master File (TMF) is set-up and maintained in "audit ready" condition; and conduct critical documentation collection and ...
New
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
Clinical Project Coordinator
Raleigh, NC · On-site
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
... Associate (CRA) management; provide support for site management activities * Develop initial drafts of clinical project plans, manuals, presentations, and other clinical project documents; assist in ...
Facilitate communication between clinical sites and BD stakeholders (e.g., Clinical Project Managers, Clinical Research Associates), as needed. * Communicate BD product complaints and other events ...
Facilitate communication between clinical sites and BD stakeholders (e.g., Clinical Project Managers, Clinical Research Associates), as needed. * Communicate BD product complaints and other events ...
Clinical Project Associate information
See salary details
$12.74 - $16.61
3% of jobs
$16.61 - $20.48
18% of jobs
$21.24 is the 25th percentile. Wages below this are outliers.
$20.48 - $24.34
20% of jobs
The median wage is $26.69 / hr.
$24.34 - $28.21
15% of jobs
$28.21 - $32.08
11% of jobs
$32.08 - $35.95
4% of jobs
$39.24 is the 75th percentile. Wages above this are outliers.
$35.95 - $39.82
5% of jobs
$39.82 - $43.68
8% of jobs
$43.68 - $47.55
6% of jobs
$47.55 - $51.42
6% of jobs
$51.42 - $55.29
3% of jobs
$12
$31
$55
How much do clinical project associate jobs pay per hour?
As of Aug 2, 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 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 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 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 is the difference between Clinical Project Associate vs Clinical Research Coordinator?
| Aspect | Clinical Project Associate | Clinical Research Coordinator |
|---|---|---|
| Credentials | Bachelor's degree often required; certifications like CCRP beneficial | Bachelor's degree in health or related field; certifications like CCRP common |
| Work Environment | Typically works with project teams, sponsors, and CROs in clinical trial settings | Works directly with patients, investigators, and site staff at clinical trial sites |
| Employer & Industry | Pharmaceutical companies, CROs, biotech firms | Hospitals, clinics, research sites |
| Search & Comparison Intent | High overlap in responsibilities and certifications | Similar 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.
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Re-posted 10 days ago
Job description
An ideal candidate for our Clinical Project Associate position is an individual who can prioritize and multitask, is experienced in windows-based computer applications, and possesses strong communication skills. The right individual will have strong time management skills and works well in a fast-paced environment.
About canfield scientific
Sourced by ZipRecruiter
Industry
Biotechnology research and development
Company size
51 - 200 Employees
Headquarters location
Parsippany, NJ, US
Year founded
1987