Clinical Research Associate
San Jose, CA · On-site
Candidate with Academic CRO experience would also be fine, leading the study(3-4 studies ... CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project ...
Clinical Research Associate
San Jose, CA · On-site
Candidate with Academic CRO experience would also be fine, leading the study(3-4 studies ... CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project ...
Clinical Research Associate II Redwood City, California, United States
Redwood City, CA · On-site
$129.40 - $152.30/hr
... CRA or field monitor, at least some of which was in a big pharma or big CRO setting * Additional experience in the pharmaceutical industry is desirable Preferred Skills & Experience * Knowledge of ...
Clinical Research Associate II Redwood City, California, United States
Redwood City, CA · On-site
$129.40 - $152.30/hr
... CRA or field monitor, at least some of which was in a big pharma or big CRO setting * Additional experience in the pharmaceutical industry is desirable Preferred Skills & Experience * Knowledge of ...
Senior Clinical Research Associate
South San Francisco, CA · On-site
$115K - $121K/yr
Bachelor's degree in life sciences or related field preferred * 2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment) * Strong understanding of GCP, ICH guidelines ...
Senior Clinical Research Associate
South San Francisco, CA · On-site
$115K - $121K/yr
Bachelor's degree in life sciences or related field preferred * 2 - 5+ years of CRA or clinical research experience (biotech, pharma, or CRO environment) * Strong understanding of GCP, ICH guidelines ...
Experience Required 4+ years as a CRA within Biotech/Pharma, Academia or CRO Education Required Bachelor's Degree, preferably in biological science. Travel Required Yes, up to 10% Core ...
Experience Required 4+ years as a CRA within Biotech/Pharma, Academia or CRO Education Required Bachelor's Degree, preferably in biological science. Travel Required Yes, up to 10% Core ...
Senior Clinical Research Associate
Newark, CA · Hybrid
$135K - $150K/yr
Experience Required 4+ years as a CRA within Biotech/Pharma, Academia or CRO Education Required Bachelor's Degree, preferably in biological science. Travel Required Yes, up to 10% Core ...
Senior Clinical Research Associate
Newark, CA · Hybrid
$135K - $150K/yr
Experience Required 4+ years as a CRA within Biotech/Pharma, Academia or CRO Education Required Bachelor's Degree, preferably in biological science. Travel Required Yes, up to 10% Core ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Clinical Research Associate II
Alameda, CA · On-site
$81K - $141K/yr
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
The Opportunity The CRA II will assist in the clinical execution and management of all aspects of ... CRO) selection and management, selection and training of investigator sites, planning and running ...
Creates a process for developing distribution, reviews, and tracking essential trial documents and/or oversees CRO or CRA responsibility for essential documents * Collaborates with team CRAs to ...
Creates a process for developing distribution, reviews, and tracking essential trial documents and/or oversees CRO or CRA responsibility for essential documents * Collaborates with team CRAs to ...
Creates a process for developing distribution, reviews, and tracking essential trial documents and/or oversees CRO or CRA responsibility for essential documents * Collaborates with team CRAs to ...
Creates a process for developing distribution, reviews, and tracking essential trial documents and/or oversees CRO or CRA responsibility for essential documents * Collaborates with team CRAs to ...
Sr Clinical Study Manager
San Diego, CA · On-site
$140 - $190/hr
Work with CRO to revise scope of service agreements, budgets, plans, and detailed timelines, and ... Coordinate/plan investigator meetings and/or site and CRA training. * Perform financial management ...
Sr Clinical Study Manager
San Diego, CA · On-site
$140 - $190/hr
Work with CRO to revise scope of service agreements, budgets, plans, and detailed timelines, and ... Coordinate/plan investigator meetings and/or site and CRA training. * Perform financial management ...
* Works collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and ... Qualifications Need to have 3-5 years of experience in data management( Pharma/ CRO/ Institute ...
* Works collaboratively with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and ... Qualifications Need to have 3-5 years of experience in data management( Pharma/ CRO/ Institute ...
Sr Clinical Study Manager
San Diego, CA · On-site
$150K - $190K/yr
Work with CRO to revise scope of service agreements, budgets, plans, and detailed timelines, and ... Coordinate/plan investigator meetings and/or site and CRA training. * Perform financial management ...
Sr Clinical Study Manager
San Diego, CA · On-site
$150K - $190K/yr
Work with CRO to revise scope of service agreements, budgets, plans, and detailed timelines, and ... Coordinate/plan investigator meetings and/or site and CRA training. * Perform financial management ...
Clinical Trial Manager
Sonoma, CA · On-site
Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program ... and CRO coordination. Start-up through close-out, not one narrow slice of it. At the CPM end ...
New
Clinical Trial Manager
Sonoma, CA · On-site
Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program ... and CRO coordination. Start-up through close-out, not one narrow slice of it. At the CPM end ...
New
Clinical Trial Manager
Santa Rosa, CA · On-site
Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program ... and CRO coordination. Start-up through close-out, not one narrow slice of it. At the CPM end ...
New
Clinical Trial Manager
Santa Rosa, CA · On-site
Clinical Operations Team Build | Bay Area | CTA/ CRA, Clinical Trial Manager, and Clinical Program ... and CRO coordination. Start-up through close-out, not one narrow slice of it. At the CPM end ...
New
Cro Cra information
What is a CRO cra?
CRO CRAs, or Clinical Research Associates working for Contract Research Organizations (CROs), are professionals who monitor clinical trials to ensure compliance with regulatory requirements and study protocols. They act as the link between the sponsor of the clinical trial and the sites conducting the research. Their responsibilities include site selection, study initiation, monitoring visits, data verification, and ensuring patient safety. CRO CRAs often work on multiple studies for different sponsors, providing flexibility and exposure to a variety of therapeutic areas.
What are some of the most common challenges faced by a CRO (Conversion Rate Optimization) manager, and how can they be addressed?
A CRO Manager often faces challenges such as aligning optimization strategies with broader business goals, managing stakeholder expectations, and balancing short-term wins with long-term improvements. It's essential to establish clear communication with marketing, product, and development teams to ensure experiments are prioritized effectively. Data-driven decision making, consistent A/B testing, and staying updated on user behavior trends can help overcome these challenges and drive meaningful results.
What are the key skills and qualifications needed to thrive as a CRO (Chief Revenue Officer), and why are they important?
To thrive as a Chief Revenue Officer (CRO), you need a strong background in sales, marketing, business development, and financial management, often supported by a relevant degree and significant leadership experience. Familiarity with CRM platforms (like Salesforce), analytics tools, and revenue management systems is typically required. Outstanding strategic thinking, communication, and cross-functional leadership skills set exceptional CROs apart. These competencies are essential for driving company growth, aligning teams, and optimizing revenue streams in a competitive market.
Is it hard to get a CRA job?
Securing a CRA (Clinical Research Associate) position can be competitive, often requiring a relevant degree in life sciences or healthcare, along with experience in clinical trials. Strong knowledge of Good Clinical Practice (GCP) guidelines and certification such as CCRP can improve job prospects, but the hiring process may involve multiple interviews and assessments of technical skills.
What are popular job titles related to Cro Cra jobs in California?
For Cro Cra jobs in California, the most frequently searched job titles are:
What job categories do people searching Cro Cra jobs in California look for?
The top searched job categories for Cro Cra jobs in California are:
- Clinical Research Associate Sponsor Dedicated
- Clinical Research Manager
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- Cra Training
- Work From Home Medical Device Clinical Research
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- Medical Device Clinical Research Manager
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- Clinical Research Study Manager
What cities in California are hiring for Cro Cra jobs?
Cities in California with the most Cro Cra job openings:
Contractor
Re-posted 8 days ago
Job description
Company Description
IRI believes in commitment, Integrity and strategic workforce solutions.
Integrated Resources, Inc., is led by a seasoned team with combined decades in the industry. We deliver strategic workforce solutions that help you manage your talent and business more efficiently and effectively. Since launching in 1996, IRI has attracted, assembled and retained key employees who are experts in their fields. This has helped us expand into new sectors and steadily grow.
We've stayed true to our focus of finding qualified and experienced professionals in our specialty areas. Our partner-employers know that they can rely on us to find the right match between their needs and the abilities of our top-tier candidates. By continually exceeding their expectations, we have built successful ongoing partnerships that help us stay true to our commitments of performance and integrity.
Our team works hard to deliver a tailored approach for each and every client, critical in matching the right employers with the right candidates. We forge partnerships that are meant for the long term and align skills and cultures. At IRI, we know that our success is directly tied to our clients' success.
Job Description
Candidate with Academic CRO experience would also be fine, leading the study(3-4 studies)
Understands data management and documentation process
Candidate who has worked on clinical trials as clinical data manager, CRF design and clinical data management plan, study maintenance
Works with Clinical Programmers, CRA, Statistical Programmers, Biostatisticians and other Clinical, DSPH, Regulatory and Project Management staff to meet project deliverables and timelines for clinical data acquisition, quality checking and reporting.
Demonstrates a general understanding of each assigned protocol, critical tasks and milestones.
Ensure completeness, correctness and consistency of routine clinical data and data structure.
Assists in the implementation of routine clinical data management process with vendors including data entry, data quality checking, data transfer, reporting, backup, and recovery. Assists in the preparation of CRF/eCRF for data collection through the regulatory approval process.
Assists in implementing routine clinical research projects.
Reviews study protocol and assists site coordinators, investigators, and field clinical staff in collecting routine data to meet the protocol requirements in a timely manner.
Identifies, tracks, and resolves routine queries.
Utilizes routine reports to track study progress and ensures timeliness and quality expectations are met.
The ability to problem solve and have people/project leadership skills.Knowledge of FDA regulations, support of needs for NDA and other regulatory submissions, and familiarity with web-based Electronic Data Capture (EDC) and clinical data management systems.
Additional Information
Regards,
Indu Dubey
Clinical Recruiter
732-844-8725
indu @irionline.com
About Integrated Resources
Sourced by ZipRecruiter
Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.
Industry
Recruiting and staffing services
Company size
51 - 200 Employees
Headquarters location
Edison, NJ, US
Year founded
1996