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Cra Clinical Research Jobs (NOW HIRING)

Emmes

Sr. In-House CRA

Rockville, MD · On-site +1

At Emmes Group , we're shaping the future of clinical research- where human intelligence meets ... The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts.

Emmes Group

Sr. In-House CRA

Rockville, MD · On-site

At Emmes Group , we're shaping the future of clinical research- where human intelligence meets ... The Sr. In-House CRA may also be referred to as a Clinical Trial Associate on some contracts.

Merck & Co.

Following the country strategy defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

Merck & Co.

Following the country strategy defined by CRD and/or CRA-Manager, contributes to the identification of new potential sites and works closely with them to develop strong clinical research capabilities.

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How much do cra clinical research jobs pay per hour?

As of Sep 9, 2026, the average hourly pay for cra clinical research 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?

CRA Clinical Research Associates are professionals who monitor clinical trials to ensure they are conducted according to regulatory requirements, protocols, and ethical guidelines. They act as the main point of contact between the study sponsor and the research sites, overseeing the progress and quality of the clinical trials. CRAs are responsible for verifying data, ensuring participant safety, and maintaining accurate documentation, playing a crucial role in bringing new medical treatments to market.

What are some common challenges a clinical research associate faces when monitoring clinical trial sites?

One of the main challenges CRAs encounter is ensuring protocol compliance across multiple sites, which may involve frequent travel and adapting to different team dynamics. Managing documentation, maintaining high data quality, and addressing issues like delayed patient recruitment or missing data are also common hurdles. Effective communication with site staff and sponsors is crucial to resolve problems quickly and keep studies on track. Additionally, balancing administrative tasks with on-site monitoring responsibilities can require strong organizational skills.

What are the key skills and qualifications needed to thrive as a clinical research associate, and why are they important?

To thrive as a Clinical Research Associate (CRA), you need a solid understanding of clinical trial protocols, regulatory guidelines (such as ICH-GCP), and often a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and certifications like ACRP or SOCRA are highly valued. Strong organizational skills, attention to detail, and effective communication are crucial soft skills for managing study sites and stakeholder relationships. These competencies ensure the integrity, compliance, and smooth execution of clinical research projects.

What is the difference between Cra Clinical Research vs Clinical Research Associate?

AspectCra Clinical ResearchClinical Research Associate
CredentialsBachelor's degree, often in life sciences; certifications like CCRP or RACBachelor's degree in life sciences or related field; certifications like CCRP or RAC
Work EnvironmentPharmaceutical companies, CROs, clinical trial sitesMonitoring clinical trials at sites, coordinating with sponsors and investigators
Industry UsageCommonly used term for roles in clinical researchMost frequently used job title for clinical trial monitors

Both Cra Clinical Research and Clinical Research Associate roles involve monitoring clinical trials, ensuring compliance, and data accuracy. The terms are often used interchangeably, but 'Cra Clinical Research' emphasizes the role within the broader clinical research field, while 'Clinical Research Associate' is the specific job title for professionals performing trial monitoring and site management.

Is it hard to get a CRA Clinical Research job?

Securing a CRA (Clinical Research Associate) position can be competitive, often requiring relevant education, such as a degree in life sciences or healthcare, and experience with clinical trial protocols. Strong organizational skills, knowledge of regulatory requirements, and certifications like the CCRA can improve job prospects, but entry may be challenging for those without related experience or training.

What does a CRA Clinical Research do in clinical research?

A CRA (Clinical Research Associate) monitors clinical trials to ensure compliance with study protocols, Good Clinical Practice (GCP), and regulatory requirements. They oversee site activities, verify data accuracy, and ensure patient safety, often using electronic data capture systems and working closely with investigators and sponsors throughout the trial process.
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Cra Clinical Research jobs near you
Infographic showing various Cra Clinical Research job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 16% Part Time, and 7% Contract. Highlights an 85% Physical, 1% Hybrid, and 14% Remote job distribution, with an average salary of $85,542 per year, or $41.1 per hour.

Clinical Research Associate (CRA) - U.S. Expert Network | Project Opportunities | Remote

Manhattan, NY • On-site

Alcedis GmbH
See more jobs at Alcedis GmbHexternal

$100 - $125/hr

Other

Posted 7 days ago

Job description

Alcedis is a well-established and successful clinical research organization headquartered in Germany, with over 30 years of experience in clinical research. Building on our strong track record in Germany, we are now taking the next step in our international growth by establishing our presence in the United States. As part of this expansion, we are building a network of experienced clinical research professionals who can support our current and future clinical studies.

We are looking for experienced Clinical Research Associates (CRAs) to join our U.S.-based expert network. Our current and anticipated projects focus primarily on Oncology and Alzheimer’s disease, with additional therapeutic areas expected to follow. Depending on project needs and mutual availability, members of our network may have the opportunity to support Alcedis as part-time W-2 employees on a project basis within our Clinical Operations team.

We are looking for a limited number of experienced CRAs to build a strong network of trusted clinical research professionals. Candidates will be reviewed based on their experience, qualifications, and fit with our current and future project needs.

When a suitable project becomes available, we will contact you to discuss the study, timing, workload, and your availability. If there is a mutual fit, you will be engaged as a part-time W-2 employee for the duration of the project.

You are welcome to continue working with other clients outside of your agreed assignment, subject to confidentiality and conflict-of-interest requirements.

Joining the expert network does not guarantee a project or minimum hours. If required, any project-specific qualification or pre-engagement activities involving actual work beyond the application and selection process will be compensated.

Qualifications and requirements

Required:

  • 3+ years of hands-on experience working as a Clinical Research Associate (CRA) / Clinical Monitor
  • Experience in GCP-regulated interventional clinical trials
  • Demonstrated experience in oncology clinical trials
  • Hands-on experience with digital solutions for clinical trials, such as ePRO, eCOA, and eCRF systems
  • Ability to work independently and proactively with a high degree of ownership
  • Experience with on-site monitoring and remote monitoring activities
  • Willingness to conduct and support Site Initiation Visits (primarily virtually) in the U.S. and Canada
  • Strong communication and organizational skills
  • Excellent written and spoken English
  • Based in the United States

Preferred:

  • Experience in Neurology and/or Alzheimer’s disease is a strong plus
  • Experience working in international or cross-border clinical research teams
  • Ability and flexibility to collaborate effectively across U.S. and European time zones, including regular interaction with colleagues based in Germany
  • Experience with U.S. and Canadian clinical trial requirements
  • Familiarity with FDA regulations, HIPAA, and 21 CFR Part 11

We welcome applicants of all backgrounds and do not discriminate based on race, ethnicity, gender, sexual orientation, disability, age, religion, or any other protected characteristic.

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