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Clinical Research Associate Ii Jobs (NOW HIRING)

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

CRA II or Senior CRA-US-Remote ICON is a global healthcare intelligence and clinical research ... ICON plc is seeking an experienced Senior Clinical Research Associate (Senior CRA) or Clinical ...

Overview Clinical Research Associate II US Remote Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing the promise of new medical ...

Clinical Research Associate 2

Fremont, CA · On-site +1

$120K - $145K/yr

The Clinical Research Associate is responsible for managing clinical operations projects, which ... Minimum of 2+ years working in industry or academics in clinical operations for medical devices.

Clinical Research Associate 2

Fremont, CA · On-site

$120K - $145K/yr

The Clinical Research Associate is responsible for managing clinical operations projects, which ... Minimum of 2+ years working in industry or academics in clinical operations for medical devices.

Clinical Research Associate II Location : This position is based in our Campbell, California offices. This position is on-site, full-time + Travel Considerations. Why Imperative Care? Do you want to ...

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Clinical Research Associate Ii information

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$12

$41

$69

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

As of Jul 16, 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 are Clinical Research Associate IIs?

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 much does a CRA II make at Iqvia?

A Clinical Research Associate II at IQVIA typically earns between $65,000 and $85,000 annually, depending on experience, location, and certifications. The role involves monitoring clinical trials, ensuring compliance, and may include travel requirements.

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, and why are they important?

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 other jobs can a clinical research associate do?

A Clinical Research Associate II can transition into roles such as clinical project manager, regulatory affairs specialist, or data manager, leveraging skills in study coordination, compliance, and data analysis. They may also move into medical writing, quality assurance, or roles in pharmaceutical or biotech companies that require knowledge of clinical trial processes and regulations.

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.

How much does a CRA II make at Icon?

A Clinical Research Associate II (CRA II) at Icon typically earns between $65,000 and $85,000 annually, depending on experience, location, and certifications. The role involves monitoring clinical trials, ensuring compliance, and working with clinical data management tools.

What is a clinical research associate II?

A Clinical Research Associate II is a professional responsible for monitoring clinical trials to ensure compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. They typically conduct site visits, review data, and communicate with study sites, often requiring relevant certifications and experience in clinical research. This role involves working closely with study teams and may require travel and proficiency with clinical trial management systems.
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 July 2026, with employment types broken down into 1% As Needed, 67% Full Time, 30% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% 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

Clinical Research Associate II or Clinical Research Associate II RN - Bioethics Program

St. Jude Children's Research Hospital

Memphis, TN • On-site

Full-time

Re-posted 10 days ago


St. Jude Children's Research Hospital rating

8.4

Company rating: 8.4 out of 10

Based on 9 frontline employees who took The Breakroom Quiz

64th of 1,020 rated hospitals


Job description

The World's Best Stop at Nothing
There's a reason St. Jude Children's Research Hospital is consistently ranked on Glassdoor's "Best Places to Work" 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. There'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 Children'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 - Dr. Liza-Marie Johnson, whose scholarship focuses on clinical and research ethics with particular emphasis on informed consent, patient-provider communication, and the ethics of novel interventions - and Dr. Meaghann Weaver, whose work spans bioethics, palliative care, quality of life, and end-of-life decision-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 decision-making with seriously ill children and their families, the allocation of emerging therapies, and the experience of suffering and end-of-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.
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 quality-of-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 focus-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 cross-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 Non-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 $70,720 - $126,880 per year for the role of Clinical Research Associate II or Clinical Research Associate II RN - Bioethics Program.
Explore our exceptional benefits!
St. Jude is an Equal Opportunity Employer
No Search Firms
St. 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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