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.
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.
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 ...
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 ...
Excellent employment opportunity for a Clinical Project Associate - II in the Foster City, CA area. * Tracking and preparing study-specific information utilizing databases, spreadsheets, and other ...
Excellent employment opportunity for a Clinical Project Associate - II in the Foster City, CA area. * Tracking and preparing study-specific information utilizing databases, spreadsheets, and other ...
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 ...
Associate Clinical Project Manager
Tempe, AZ · On-site
Job Responsibilities: (Primary Duties, Roles, and/or Authorities) Under direct manager supervision, the Associate Clinical Project Manager will: * Manage the quality and compliance of assigned ...
Associate Clinical Project Manager
Tempe, AZ · On-site
Job Responsibilities: (Primary Duties, Roles, and/or Authorities) Under direct manager supervision, the Associate Clinical Project Manager will: * Manage the quality and compliance of assigned ...
Job Responsibilities: (Primary Duties, Roles, and/or Authorities) Under direct manager supervision, the Associate Clinical Project Manager will: * Manage thequality and compliance of assigned ...
Job Responsibilities: (Primary Duties, Roles, and/or Authorities) Under direct manager supervision, the Associate Clinical Project Manager will: * Manage thequality and compliance of assigned ...
Clinical Project Manager III
Bedford, MA · On-site
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 Project Manager III
Bedford, MA · On-site
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 Project Manager III
Bedford, MA · On-site
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 Project Manager III
Bedford, MA · On-site
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 ...
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 ...
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 ...
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 Project Manager III
Bedford, MA · On-site
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 Project Manager III
Bedford, MA · On-site
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 Project Manager / Sr. Clinical Project Manager
Baltimore, MD · On-site
$100K - $135K/yr
Associates / equivalency (60 or more college credit hours) in related field + 2 years as a Project Manager; OR Bachelor of Science in related field + 1 year as a Project Manager. 3 years of Project ...
Quick apply
Clinical Project Manager / Sr. Clinical Project Manager
Baltimore, MD · On-site
$100K - $135K/yr
Associates / equivalency (60 or more college credit hours) in related field + 2 years as a Project Manager; OR Bachelor of Science in related field + 1 year as a Project Manager. 3 years of Project ...
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 ...
Quick apply
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 ...
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 ...
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?
What are the key skills and qualifications needed to thrive as a Clinical Project Associate, and why are they important?
What are the typical responsibilities of a Clinical Project Associate in supporting clinical trial operations?
What is a Clinical Project Associate?
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.

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.
- 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.