Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Manage assigned operational aspects of clinical studies from study start through database lock ...
Clinical Research Associate (CRA) - Temporary Location: Waltham, MA Schedule: Flexible hours, about ... Manage assigned operational aspects of clinical studies from study start through database lock ...
... CRA responsible sites, and assessing overall status of the project; * Develop the project ... proceed with study start and conduct in compliance with protocol and relevant regulations;
Quick apply
... CRA responsible sites, and assessing overall status of the project; * Develop the project ... proceed with study start and conduct in compliance with protocol and relevant regulations;
... CRA responsible sites, and assessing overall status of the project; * Develop the project ... proceed with study start and conduct in compliance with protocol and relevant regulations;
Quick apply
... CRA responsible sites, and assessing overall status of the project; * Develop the project ... proceed with study start and conduct in compliance with protocol and relevant regulations;
Sr CRA- Responsibilities * Develops strong site relationships and ensures continuity of site ... Collects, reviews, and monitors required regulatory documentation for study start-up, study ...
Sr CRA- Responsibilities * Develops strong site relationships and ensures continuity of site ... Collects, reviews, and monitors required regulatory documentation for study start-up, study ...
Sr CRA- Responsibilities Develops strong site relationships and ensures continuity of site ... Collects, reviews, and monitors required regulatory documentation for study start-up, study ...
Sr CRA- Responsibilities Develops strong site relationships and ensures continuity of site ... Collects, reviews, and monitors required regulatory documentation for study start-up, study ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Dallas, TX · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Dallas, TX · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Phoenix, AZ · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Phoenix, AZ · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Flagstaff, AZ · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Clinical Research Associate (CRA) - Cardiovascular/Vaccine/Infectious Disease- Remote
Flagstaff, AZ · On-site
Collects, reviews, and monitors required regulatory documentation for study start-up, study ... Contributes to CRA team knowledge by acting as process Subject Matter Expert (SME), buddy/mentor ...
Study Clinician
$54K - $71K/yr
Work closely with sites to proactively identify, manage and timely resolve study start-up up ... Must be proficient in collaborative problem-solving skills (A prior CRA or someone with Study ...
Study Clinician
$54K - $71K/yr
Work closely with sites to proactively identify, manage and timely resolve study start-up up ... Must be proficient in collaborative problem-solving skills (A prior CRA or someone with Study ...
Study Start Cra information
See salary details
$12.02 - $17.26
0% of jobs
$17.26 - $22.51
8% of jobs
$22.51 - $27.75
13% of jobs
$29.16 is the 25th percentile. Wages below this are outliers.
$27.75 - $33
15% of jobs
$33 - $38.24
13% of jobs
The median wage is $39.03 / hr.
$38.24 - $43.49
11% of jobs
$43.49 - $48.73
12% of jobs
$50.59 is the 75th percentile. Wages above this are outliers.
$48.73 - $53.98
13% of jobs
$53.98 - $59.22
14% of jobs
$59.22 - $64.47
2% of jobs
$64.47 - $69.71
1% of jobs
$12
$41
$69
How much do study start cra jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for study start cra in the United States is $41.13, according to ZipRecruiter salary data. Most workers in this role earn between $28.85 and $52.64 per hour, depending on experience, location, and employer.
What are popular job titles related to Study Start Cra jobs?
For Study Start Cra jobs, the most frequently searched job titles are:
CRA II
Exton, PA • Remote
System One
• Business Consulting Services • 5 - 10K employees5,001 - 10,000 employees
$82K - $107K/yr
Full-time
Medical, Dental, Vision, Life, Retirement
Re-posted 28 days ago
Job description
Job Title: CRA II Location: Must be Mid-West based in the United States Type: Direct Hire, full time permanent direct with the client Salary Range: $82,000 - $107,000 commemorate with level of experience Model: Hybrid – onsite and remote Hours: 40.0 Looking for your next step as a CRA? This is an opportunity to join a fast-moving medical device organization where you'll have meaningful ownership, strong visibility within Clinical Operations, and the ability to contribute to studies that can directly impact patient outcomes.
Responsibilities
- Maintain TMF and regulatory documentation ensuring ICH/GCP and SOP compliance; oversee IRB approvals, informed consent quality, investigational device accountability, and complete/accurate reporting of AEs and protocol-required data.
- Support study start-up and site readiness, conduct site training, manage study supplies and tracking systems, resolve queries/DCFs, and identify/implement corrective actions for protocol deviations across multiple concurrent studies.
- Drive communication through team meetings, status reporting, and milestone tracking; support audits and site payments, lead documentation updates, and contribute to SOP enhancements and operational best practices.
- Bachelor’s Degree, or RN required
- 2+ years monitoring experience
- 3+ Clinical Research Coordinator experience
- Class III Medical Device experience required
- ICU (and therefore hospital) and site management experience required
- Ability to travel 2-4 times/month (depends on volume of need)
System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.
System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.
#M- #LI- #LI-ES1 Ref: #568-Clinical
About System One
Sourced by ZipRecruiter
System One helps employers get work done more efficiently and economically without compromising quality. Over our 35+ year history, we've helped connect thousands of talented people with innovative companies. The excitement of a perfect fit motivates us every single day.
Industry
Business consulting services and recruiting and staffing services
Company size
5,001 - 10,000 Employees
Headquarters location
Pittsburgh, PA, US