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Clinical Research Associate Ii Jobs (NOW HIRING)

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 ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

IQVIA is hiring a Clinical Research Associate 2 with on-site monitoring experience in IM/GI, MASH/NASH, dermatology and/or asthma/respiratory clinical trials. Women's Health experience is a plus! Job ...

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal ...

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal ...

We are currently seeking a Senior Clinical Research Associate or Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal ...

SystImmune is seeking a high quality, ambitious and experienced Clinical Research Associate II (CRA II) to support SystImmune's clinical trials. The CRA II is responsible for the management and ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Our clinical and academic facilities are located throughout the state including New Brunswick ... The Research Associate II will work with the Executive Director and Assistant Director to collect ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

Clinical Research Associate II

Alameda, CA · On-site

$81K - $141K/yr

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

$91K - $114K/yr

Minimum of 2 years of experience as a Clinical Research Associate. * In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines. * Strong organizational and communication ...

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Clinical Research Associate Ii information

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How much do clinical research associate ii jobs pay per hour?

As of Aug 8, 2026, the average hourly pay for clinical research associate ii 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 is a clinical research associate ii?

Clinical Research Associate IIs are professionals who monitor and manage clinical trials to ensure that they are conducted in compliance with regulatory requirements and study protocols. They are responsible for overseeing the progress of clinical research at various sites, ensuring accurate data collection, and maintaining patient safety. Typically, a CRA II has more experience than an entry-level CRA, taking on additional responsibilities such as mentoring junior staff and handling more complex studies. Their work is crucial in bringing new medical treatments and devices to market.

How does a clinical research associate ii typically collaborate with investigators and study coordinators at clinical trial sites?

As a Clinical Research Associate II, you will regularly interact with investigators and study coordinators to ensure that clinical trials are conducted according to protocol, regulatory requirements, and good clinical practice (GCP) guidelines. This often involves performing site visits, providing ongoing training, resolving study-related queries, and verifying accurate data collection and documentation. Building strong professional relationships and maintaining clear communication are key, as you will serve as a primary liaison between the sponsor and site staff, helping to address challenges and keep studies on track.

What are the key skills and qualifications needed to thrive as a clinical research associate ii?

To thrive as a Clinical Research Associate II, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP), and a relevant bachelor’s degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, regulatory submission processes, and certifications such as ACRP or SOCRA are commonly required. Attention to detail, effective communication, and strong organizational skills set outstanding candidates apart in this role. These competencies are crucial for ensuring compliance, data integrity, and the successful management of clinical trials.

What is the difference between Clinical Research Associate II vs Clinical Research Associate I?

AspectClinical Research Associate IClinical Research Associate II
Required CredentialsBachelor's degree, some certifications (e.g., CCRP optional)Same as CRA I, often with additional experience
Work EnvironmentEntry-level, supporting clinical trials under supervisionMore independent, handling complex trials
Employer & Industry UsagePharmaceutical, biotech, CROsSame as CRA I, with increased responsibilities
Common Search & ComparisonOften compared with CRA II for career progressionHigher level role with more experience required

The main difference between Clinical Research Associate II and Clinical Research Associate I lies in experience and independence. CRA II professionals typically handle more complex trials and work more independently, while CRA I roles are more supportive and entry-level. Both roles require similar educational backgrounds and certifications, but CRA II positions demand greater experience and expertise.

More about Clinical Research Associate Ii jobs
What cities are hiring for Clinical Research Associate Ii jobs? Cities with the most Clinical Research Associate Ii job openings:
What are the most commonly searched types of Clinical Research Ii jobs? The most popular types of Clinical Research Ii jobs are:
What states have the most Clinical Research Associate Ii jobs? States with the most job openings for Clinical Research Associate Ii jobs include:
Infographic showing various Clinical Research Associate Ii job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate II and Senior Clinical Research Associate

ClinChoice

Full-time

Re-posted 9 hours ago


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

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