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Cra Positions Jobs (NOW HIRING)

Cathay Bank

CRA Administration Officer

El Monte, CA · On-site

$33.65 - $48.08/hr

Acts as a backup for other department positions when others are out of the office. Represents the Bank at various community events and fundraisers, acts as a champion for the CRA team at internal ...

IQVIA

CRA 2/Senior CRA

Sacramento, CA · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

Dallas, TX · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

New York, NY · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

Chicago, IL

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

Carlsbad, CA · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

Houston, TX

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

IQVIA

CRA 2/Senior CRA

New York, NY · On-site

$90K - $175K/yr

IQVIA Biotech is seeking CRA 2 and Sr. CRA 1 candidates with onsite monitoring experience in ... Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may ...

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Cra Positions information

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$11K

$79.4K

$137.5K

How much do cra positions jobs pay per year?

As of Jun 21, 2026, the average yearly pay for cra positions in the United States is $79,437.00, according to ZipRecruiter salary data. Most workers in this role earn between $33,000.00 and $136,500.00 per year, depending on experience, location, and employer.

Is it hard to get a CRA job?

Getting a CRA (Clinical Research Associate) position can be competitive, as it often requires relevant education, such as a degree in life sciences or healthcare, and experience with clinical trials. Strong organizational skills, knowledge of Good Clinical Practice (GCP), and certifications like the CCRP can improve chances of employment, but the hiring process may still be challenging depending on the job market and experience level.

What are CRA positions?

CRA positions, or Clinical Research Associate positions, are roles within the clinical research field responsible for monitoring clinical trials to ensure compliance with regulatory requirements and study protocols. CRAs act as a bridge between the trial sponsor and the clinical site, overseeing the progress of clinical studies, verifying data accuracy, and ensuring participant safety. These professionals typically travel to different research sites, work closely with site staff, and help resolve any issues that arise during the study. CRA positions are crucial in the process of bringing new drugs, devices, or treatments to market safely and efficiently.

What is a CRA job position?

A CRA (Clinical Research Associate) is responsible for monitoring clinical trials to ensure compliance with regulatory requirements and study protocols. They typically conduct site visits, review data, and communicate with investigators, often requiring knowledge of Good Clinical Practice (GCP) and relevant software tools. The role usually requires a bachelor's degree in a related field and certification such as CCRP.

What are the key skills and qualifications needed to thrive as a Clinical Research Associate (CRA), and why are they important?

To thrive as a Clinical Research Associate, you need a solid background in life sciences or a related field, understanding of clinical trial protocols, and often a bachelor's degree or higher. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification are commonly required. Attention to detail, strong organizational skills, and effective communication set top-performing CRAs apart. These competencies ensure compliance, data integrity, and smooth collaboration across research teams, which are critical for the success of clinical studies.

What are some common challenges faced by Clinical Research Associates (CRAs) and how can they be managed effectively?

Clinical Research Associates often encounter challenges such as frequent travel, managing multiple study sites, and ensuring strict compliance with regulatory requirements. Staying organized and maintaining clear communication with site staff are key to overcoming these hurdles. Many CRAs also develop strong time management skills to balance administrative tasks with on-site monitoring visits. Proactively building relationships with site teams and leveraging electronic data capture systems can also help streamline workflow and minimize stress.

What is the salary for CRA?

The salary for a Clinical Research Associate (CRA) typically ranges from $60,000 to $110,000 annually, depending on experience, location, and the size of the organization. Entry-level CRAs usually earn around $60,000, while experienced professionals can earn over $100,000, often with additional benefits and bonuses.

Is CRA an entry level job?

A Clinical Research Associate (CRA) position is typically considered an entry-level role in clinical research, often requiring a bachelor's degree in a related field and some relevant training or certification. However, some companies may prefer candidates with prior experience or specific skills in monitoring or regulatory compliance. Advancement usually involves gaining experience and additional certifications such as CCRP or RAC.
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Clinical Research Associate (CRA) - All levels (I/II/Senior)

Theradex Oncology

Princeton, NJ • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 8 days ago

Job description

Who We Are
Celebrating 40+ years!
Theradex Oncology is a full-service CRO specializing in oncology. The company manages global oncology trials and programs. The company was founded in 1982 working with the National Cancer Institute, which led to its expansion to working with industry sponsors developing cancer therapeutics. As a service-based company we support both domestic and international sponsors in the conduct of both early and late phase trials.
What You'll Do
As part of Theradex Oncology, you will have the opportunity to work with one of the largest professional teams focused solely on the development of cancer therapies. Cancer research continues to evolve as new therapies and therapeutic approaches are discovered, as part of the team you will the work to support our sponsors in the development of these therapies. Theradex Oncology is an environment for highly motivated individuals who want to make a difference.
Opportunity
Clinical Research Associate (CRA) - All levels (I/II/Senior)
We are expanding our team and are looking to hire CRAs for onsite and remote monitoring of phase l-lll oncology studies.
The primary responsibilities of this position include, but are not limited to, the following:
Conduct Site Monitoring:
  • Site Qualification visits
  • Site Initiation visits
  • Routine Monitoring visits
  • Close-out visits
  • All aspects of site management as described in the study plans

Source document verification:
  • Verify patient eligibility
  • Reviews consent process for each subject (Informed Consent Form and source documentation)
  • Assess protocol compliance and deviations
  • CRF review and data corrections
  • IMP accountability
  • Maintenance of on-site investigator files
  • IEC/IRB documentation
  • Local laboratory documentation
  • Maintenance of investigational supplies
  • Identify and assess safety issues and reporting (SAEs/AEs)

Site Management:
  • Ensure protection of participants and participants' rights
  • Proactively identify and resolve actual and potential site and study issues
  • Ensure clinical data integrity and adherence to study timelines
  • Clinical Review of individual patient listings
  • Assist in the preparation of project specific materials e.g., status reports, newsletters, templates, etc.
  • Act as the routine liaison between study site and the project team for study related issues
  • Perform other duties as assigned by management

What You Need
Level of Education
  • At minimum, Bachelor's degree in biological or science-related field (BSc, BA, or RN equivalent) or equivalent experience.

Prior Experience
  • As a Clinical Research Associate with experience managing clinical trial sites, the number years and type of monitoring experience will determine CRA level.
  • Experience in monitoring oncology studies is preferred
  • Experience monitoring oncology Phase I-III studies required for Sr CRA consideration

Skills and Competencies
  • Knowledge of ICH/GCP Guidelines, and Regulatory requirements
  • Ongoing development of cancer therapy knowledge, clinical trial design and conduct, and drug development process through work experience, literature reviews and other educational opportunities
  • Proficient in Excel, PowerPoint, Word, and Outlook
  • Skilled remote collaboration and teleconferencing platforms
  • Strong organizational skills, including efficiency, punctuality, and collaboration in a team environment.
  • Effective communication skills: verbal and written
  • Strong interpersonal skills including presentation, persuasion, and influence

Additional Requirements
  • This position involves travel as needed to meet study requirements. Ability to travel up to 50% may involve overnight stays.
  • Valid Driver's License required and Passport preferred
  • Successfully pass background clearance checks which may be run on a periodic basis due to 3rd party contractual obligation requirements.
  • Fluent in English (written and verbal)

What We Offer
At Theradex we offer a supportive culture that puts people first. Our employees are eligible to participate in our comprehensive benefits package which includes medical, dental and vision coverage; life insurance, disability insurance (STD/LTD), company matched 401(k), very competitive tuition reimbursement, generous vacation/sick plans, flexible work schedules, employee discounts and other company provided benefits. The annual base salary for our CRA positions range from $75,000-$145,000 with bonus potential. We will assess the specific title and level of entry during the interview and assessment process since the actual salary offer will be based on a number of factors, including but not limited to the candidate's qualifications, experience, skills, and competencies for the role.
This position is not eligible for company provided sponsorship or relocation.
Theradex is not accepting assistance from search firms for this employment opportunity.
Theradex is an Equal Opportunity Employer.

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