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Clinical Research Associate 2 Jobs (NOW HIRING)

Clinical Research Associate II

Los Angeles, CA ยท On-site

$25 - $36.86/hr

The Clinical Research Associate II works independently but in close collaboration with a Clinical Research Coordinator, Research Program Administrator, Research Nurse, other supervising staff to ...

Research Associate II

Tucson, AZ ยท On-site

$27/hr

Your main responsibilities as a Research Associate II: ยท Responsible for conducting research ... Scientific, Clinical Research and Engineering. Our team offers well over 200 years of combined ...

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 ...

The Senior Clinical Research Associate II is responsible for the site management, site monitoring and close-out of assigned clinical trials investigator sites to ensure patient safety and quality ...

$90K - $110K/yr

Avania is hiring Clinical Research Associates II (CRA II) - Medical Device Clinical Trials Salary range $90,000 - $110,000 + Annual performance related bonus + Benefits - Minimum 2+ years of prior ...

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Clinical Research Associate 2 information

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How much do clinical research associate 2 jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical research associate 2 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 2?

A Clinical Research Associate 2 (CRA 2) is a mid-level professional in clinical research who is responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and maintaining the integrity of data collected during studies. They typically oversee multiple study sites, perform site visits, review trial documentation, and act as a liaison between the sponsor and the research sites. CRA 2 positions usually require prior experience as a CRA 1 or similar role and a strong understanding of Good Clinical Practice (GCP) guidelines. Their work is essential in ensuring that clinical trials are conducted ethically and that participant safety and data quality are maintained.

What are the key skills and qualifications needed to thrive as a clinical research associate 2?

To thrive as a Clinical Research Associate 2, you need a solid background in life sciences, knowledge of clinical trial protocols, and experience with regulatory requirements, often supported by a relevant degree and prior CRA experience. Familiarity with electronic data capture (EDC) systems, Good Clinical Practice (GCP) certification, and clinical trial management systems (CTMS) is typically required. Strong organizational skills, attention to detail, and effective communication help you manage multiple studies and collaborate with sites and sponsors. These skills ensure compliance, data integrity, and efficient progress of clinical trials, which are essential for advancing medical research.

What are some common challenges faced by clinical research associate 2s when monitoring multiple clinical trial sites?

As a Clinical Research Associate 2, one of the most common challenges is efficiently managing time and communication across multiple trial sites, often located in different regions. Balancing travel, site visits, and remote monitoring requires strong organizational skills and adaptability to each site's workflow. Additionally, ensuring consistent protocol adherence and data quality while building collaborative relationships with site staff can be demanding. Proactive communication and the ability to quickly resolve issues are key to overcoming these challenges.
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Infographic showing various Clinical Research Associate 2 job openings in the United States as of September 2026, with employment types broken down into 3% As Needed, 74% Full Time, 15% Part Time, and 8% 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 II or Clinical Research Associate II RN - Bioethics Program

Memphis, TN โ€ข On-site

3M HEALTHCARE
10K+ employees

Other

Posted 9 days ago


Job description

The Worldโ€™s Best Stop at Nothing

There's a reason St. Jude Childrenโ€™s Research Hospital is consistently ranked on Glassdoorโ€™s โ€œBest Places to Workโ€ list. Actually, there are more than 6,500 reasons. At our world-class pediatric research hospital, every one of our 6,500 professionals shares our commitment to making a difference in the lives of the children we serve. Thereโ€™s a unique bond when you are part of a team that will stop at nothing to advance the treatments and cures of pediatric catastrophic diseases. The result is a collaborative, positive environment where all employees, regardless of their role, receive the resources, support, and encouragement to advance and grow their careers.

The Bioethics Program at St. Jude Childrenโ€™s Research Hospital

The Bioethics Program at St. Jude Childrenโ€™s Research Hospital is a multidisciplinary program dedicated to addressing the ethical dimensions of pediatric care and cutting-edge biomedical research. The program is led by two core faculty โ€” Dr. Liza-Marie Johnson, whose scholarship focuses on clinical and research ethics with particular emphasis on informed consent, patientโ€‘provider communication, and the ethics of novel interventions โ€” and Dr. Meaghann Weaver, whose work spans bioethics, palliative care, quality of life, and endโ€‘ofโ€‘life decisionโ€‘making for seriously ill children. Together with a clinical ethicist and 2.5 clinical research associate FTE, the team provides clinical and research ethics consultation services, produces original scholarship in bioethics, and engages in organizational ethics to help shape institutional policy and culture. Research themes across the program include ethical issues in pediatric genomic sequencing, communication and decisionโ€‘making with seriously ill children and their families, the allocation of emerging therapies, and the experience of suffering and endโ€‘ofโ€‘life care in pediatric populations. The program operates at the intersection of rigorous bioethical inquiry and complex pediatric care, offering a rich environment for scholarly collaboration and meaningful clinical and organizational impact.

Clinical Research Associate II or Clinical Research Associate II RN

The Clinical Research Associate II or Clinical Research Associate II RN is responsible for performing data abstraction, collection, and entry to support clinical research. Develops, maintains, and/or monitors case report forms. Ensures compliance with prescribed interventions and evaluations of the assigned protocol(s) utilizing quantitative and qualitative methodology. Provides data and reports to the collaborating research organization or study sponsor. Helps to prepare literature searches/summations and assists in grant writing and manuscript preparation/ submission. The research team studies issues related to clinical and research ethics ranging from qualityโ€‘ofโ€‘life data, ethics analysis, to health system reviews. The CRA II or CRA II RN often partners with pediatric families impacted by serious or chronic illness such as sickle cell disease, pediatric cancer, and childhood neuromuscular disorders. Care models may include palliative, hospice, and bereavement care. This position will work primarily onsite.

Job Responsibilities
  • Act as site study coordinator recruiting participants, conducting informed consent process as designated and assisting with protocol submissions for review by federal or institutional committees (e.g. CTSRC and IRB) as applicable.
  • Develop, maintain, monitor, and/or share assigned/relevant documentation (e.g., investigator files, case report forms, study data).
  • Perform data abstraction, collection, and entry to support clinical research.
  • Conduct interviews and focusโ€‘groups with study participants.
  • Prepare submission for all reportable events (e.g., adverse events, protocol variances, violations).
  • Prepare detailed data reports as required.(As applicable)
  • Provide patient care, education, and management (e.g., routine test conduct; assistance in clinical procedures; medication instruction, monitoring, and documentation; patient care coordination; education on protocol activities).
  • Engages in literature reviews and synthesis the findings.
  • Assists in grant preparation.
  • Participates in research manuscript preparation and submissions.
  • Perform other duties as assigned to meet the goals and objectives of the department and institution.
  • Maintains regular and predictable attendance.
Minimum Education and/or Training
  • For Clinical Research Associate II: Bachelor's degree in relevant area required. Master's degree preferred, ideally in bioethics or related field.
  • For Clinical Research Associate II RN: Bachelor's degree in Nursing required. Master's degree preferred, ideally in bioethics or related field.
Minimum Experience
  • Minimum Requirement: 2+ years of experience in carrying out research preferably in healthcare settings.
  • Experience Exception: Master's degree and some experience preferred, ideally working with patient communities or in bioethics.
  • Experience managing crossโ€‘functional communication, including liaison between site and study teams.
  • Some experience with documentation and tracking systems/processes.
  • Proven performance in earlier role.
Licensure, Registration and/or Certification Required by Law
  • For Clinical Research Associate II: None.
  • For Clinical Research Associate II RN: (LC: RN-TN) Must possess a current Tennessee State Board of Nursing license if primary residence is Tennessee or a Nurse Licensure Nonโ€‘Compact state. (LC: RN-MISS, RN-ARK or RN-KY) Must possess a current State Board of Nursing license in the state of primary residence if the state is a Nurse Licensure Compact state.
Compensation

In recognition of certain U.S. state and municipal pay transparency laws, St. Jude is including a reasonable estimate of the compensation range for this role. This is an estimate offered in good faith and a specific salary offer takes into account factors that are considered in making compensation decisions including but not limited to skill sets, experience and training, licensure and certifications, and other business and organizational needs. It is not typical for an individual to be hired at or near the top of the salary range and compensation decisions are dependent on the facts and circumstances of each case. A reasonable estimate of the current salary range is $70,720โ€“$126,880 per year for the role of Clinical Research Associate II or Clinical Research Associate II RNโ€“Bioethics Program.

Explore our exceptional benefits!St. Jude is an Equal Opportunity EmployerNo Search FirmsSt. Jude Children's Research Hospital does not accept unsolicited assistance from search firms for employment opportunities. Please do not call or email. All resumes submitted by search firms to any employee or other representative at St. Jude via email, the internet or in any form and/or method without a valid written search agreement in place and approved by HR will result in no fee being paid in the event the candidate is hired by St. Jude.

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