ClinChoice is a rapidly growing global contract research organization. We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and ...
ClinChoice is a rapidly growing global contract research organization. We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and ...
Sr. Clinical Research Associate
Louisiana, MO · On-site +1
The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively ... Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.
Sr. Clinical Research Associate
Louisiana, MO · On-site +1
The Sr. CRA provides guidance to less experienced CRAs, supports investigator sites, proactively ... Provide mentoring, training, and functional oversight of CRAs, including contingent (contract) CRAs.
Marketing Specialist
California, MO · On-site
$80 - $100/hr
Coordinate media contracts and ad buys. Track promotional activities bank-wide and report to the ... Work with the Bank's Compliance/CRA Officer to ensure all products and marketing materials comply ...
Marketing Specialist
California, MO · On-site
$80 - $100/hr
Coordinate media contracts and ad buys. Track promotional activities bank-wide and report to the ... Work with the Bank's Compliance/CRA Officer to ensure all products and marketing materials comply ...
Oncology Provider Account Manager - California
California, MO · On-site
$100 - $125/hr
... companies, contract research organizations (CROs), and healthcare systems to accelerate drug ... This is not a clinical research site management / CRA / study coordinator role. Responsibilities
Oncology Provider Account Manager - California
California, MO · On-site
$100 - $125/hr
... companies, contract research organizations (CROs), and healthcare systems to accelerate drug ... This is not a clinical research site management / CRA / study coordinator role. Responsibilities
Research Project Manager - Comprehensive Integrated Research Operations (CIRO)
Kansas City, MO · On-site
$100 - $125/hr
Ensure compliance with institutional policies, sponsor requirements, contracts, agreements, and ... Certified Research Administrator (CRA), Certified Clinical Research Coordinator (CCRC), Certified ...
Research Project Manager - Comprehensive Integrated Research Operations (CIRO)
Kansas City, MO · On-site
$100 - $125/hr
Ensure compliance with institutional policies, sponsor requirements, contracts, agreements, and ... Certified Research Administrator (CRA), Certified Clinical Research Coordinator (CCRC), Certified ...
Key Account Manager(Oncology Providers) - California
California, MO · On-site
$100 - $125/hr
... companies, contract research organizations (CROs), and healthcare systems to accelerate drug ... This is not a clinical research site management / CRA / study coordinator role. Responsibilities:
Key Account Manager(Oncology Providers) - California
California, MO · On-site
$100 - $125/hr
... companies, contract research organizations (CROs), and healthcare systems to accelerate drug ... This is not a clinical research site management / CRA / study coordinator role. Responsibilities:
Senior Clinical Research Associate (Pool)
California, MO · On-site
$125 - $150/hr
... Contract Research Organization (CRO) headquartered in San Diego, CA, USA. Our mission is to bring ... The Senior Clinical Research Associate (Sr. CRA) will independently execute monitoring ...
Senior Clinical Research Associate (Pool)
California, MO · On-site
$125 - $150/hr
... Contract Research Organization (CRO) headquartered in San Diego, CA, USA. Our mission is to bring ... The Senior Clinical Research Associate (Sr. CRA) will independently execute monitoring ...
Monitor quality of existing accounts by verifying that assigned accounts conform to contract and ... procedures (i.e., CRA, Fair Lending, etc.) evidenced by appropriate application of these ...
Monitor quality of existing accounts by verifying that assigned accounts conform to contract and ... procedures (i.e., CRA, Fair Lending, etc.) evidenced by appropriate application of these ...
Contract Cra information
See Missouri salary details
$11.27 - $16.19
0% of jobs
$16.19 - $21.11
8% of jobs
$21.11 - $26.03
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$27.35 is the 25th percentile. Wages below this are outliers.
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15% of jobs
$30.95 - $35.87
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The median wage is $36.61 / hr.
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$47.45 is the 75th percentile. Wages above this are outliers.
$45.71 - $50.63
13% of jobs
$50.63 - $55.55
14% of jobs
$55.55 - $60.47
2% of jobs
$60.47 - $65.39
1% of jobs
$11
$38
$65
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What is a contract CRA?
A contract clinical research associate (contract CRA) is a temporary position in which you manage clinical trials and scientific research projects. As a contractor, you work temporarily on a contract that typically lasts for the duration of the project. Clinical research associates work in the pharmaceutical industry to ensure the safety and effectiveness of medication or vaccines. You can also work on studies for biotech companies and projects that perform analysis on surgical procedures or treatments. Your duties focus on planning the trial, defining the parameters, ensuring the safety of participants, and making sure the project meets all regulations and requirements.
What are the key skills and qualifications needed to thrive as a contract CRA, and why are they important?
What are some common challenges faced by contract CRAs and how can they effectively manage them?
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Full-time
Re-posted yesterday
Key responsibilities
Manage clinical study activities across multiple sites within one or more projects, focusing on medical devices.
Oversee site performance, conduct clinical studies, and ensure high-quality deliverables through site visits, monitoring, and communication.
Travel to sites and surrounding countries as required to perform monitoring and site management activities.
Job description
Are you a CRA looking for the best of both worlds?
Would you like to work directly with a single sponsor while still enjoying the stability, global reach, and career development opportunities that come with working for a leading CRO? Our team calls it the best of both worlds - and we think you'll agree.
ClinChoice is a rapidly growing global contract research organization. We're currently expanding our CRA network in the Netherlands and looking for talented Clinical Research Associates (CRA II and Senior CRA) interested in partnering with some of the world's leading pharmaceutical companies in the field of biomedicine.
If that sounds like you, we encourage you to submit your resume via our website - we'd love to hear from you!
Position Overview - Clinical Research Associate
As a CRA, you'll manage clinical study activities across multiple sites within one or more projects, with a focus on medical devices. You will oversee site performance, conduct company-initiated clinical studies, and ensure high-quality deliverables through site visits, monitoring, and effective communication.
Key Requirements:
Willingness to travel to sites and surrounding countries (50-80% travel).
Fluent in Dutch (required for work in the Netherlands).
Prior experience in monitoring clinical trials and site management.
Join a dynamic, global team that values growth, collaboration, and making a difference in clinical research.
Skills and Qualifications:
- Bachelor's Degree or equivalent University Degree in scientific and/or medical or paramedical disciplines; Nursing degree or relevant degree or background preferred. In some cases, an equivalency, consisting of a combination of appropriate education, training and or directly related experience, will be considered sufficient for an individual to meet the requirements of the role.
- Up to 8 years of experience as a CRA.
- Strong knowledge of clinical trial operations, GCP/ICH Guidelines, and other applicable regulatory requirements.
- Sound knowledge of medical terminology.
- Fluent in English and local language(s).
- Proficiency in Microsoft Office (e.g. Word, Excel, Outlook).
Education and Experience:
- A Bachelor Degree is required, preferably a Bachelor of Science Degree in Life Science, Physical Science, Nursing or Biological Science, a Masters or PhD/MD/PharmD.
- At least 4 plus years of onsite monitoring experience is required.
- Previous medical device monitoring experience is required. Therapeutic area experience in neuro- or cardiovascular domain is also required.
- Requires understanding and application of regulations and standards applied in clinical research areas and medical devices/combination products.
- Relevant industry certifications preferred (i.e., CCRA, RAC, CDE).
- Clinical/medical background - a plus.
- Languages: Be able to converse and monitor in English and Dutch. Must be able to converse and understand the documentation, monitoring, etc. in a reasonably confident manner to monitor in that.
- Ability to travel up to 80% of time.
The Application Process
Once you have submitted your CV, you will receive an acknowledgement that we received it. If you have the requirements we need, you will be invited for phone interview as the first step. Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
Who will you be working for?
About ClinChoice
ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.
Our Company Ethos
Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives to all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is evidenced by our below industry average turnover rates.
ClinChoice is an equal opportunity employer. We have based our success on attracting, developing, and promoting talent guided by diversity and inclusivity. Our employees come from very diverse backgrounds: gender, race, beliefs, and ethnicities. We recognize this is our strength and celebrate it.
Keywords: Senior Clinical Research Associate, Senior CRA, Freelance, Self-employed, Contract, Site Management, Monitor, Monitoring, Complex Trials, Medical Devices, Cardiology, Neurology, Open to Travel, Submissions, Ethics, Contract Research Organisation, CRO
#LI-CM1 #LI-CONTRACT #LI-1FTE
About ClinChoice
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
1,001 - 5,000 Employees
Headquarters location
Fort Washington, PA, US
Year founded
1995