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Clinical Research Associate Ii Jobs (NOW HIRING)

R&D Partners

Research Associate II

Tucson, AZ · On-site

$27/hr

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 ...

ICON

Senior Clinical Research Associate

Blue Bell, PA · On-site

Senior CRA/ CRA II ICON is a global healthcare intelligence and clinical research organisation ... As a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing ...

Emmes

Clinical Research Associate II

Rockville, MD · On-site +1

Overview Clinical Research Associate II US remotely and on-site (80% travel) Emmes Group: Building a better future for us all. Emmes Group is transforming the future of clinical research, bringing ...

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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 Aug 23, 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.

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.

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 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.

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Clinical Research Associate Ii jobs near you
Infographic showing various Clinical Research Associate Ii job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 68% Full Time, 29% 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

Cedars Sinai

Los Angeles, CA • On-site

$25 - $36.86/hr

Full-time

Re-posted 20 days ago

Cedars-Sinai rating

8.6

Company rating: 8.6 out of 10

Based on 131 frontline employees who took The Breakroom Quiz

43rd of 1,062 rated hospitals

Job description


This role is designed to be 100% onsite, giving you the opportunity to collaborate closely with your team and immerse yourself in the energy of our workplace. Please note that hybrid or remote work options are NOT available for this position at this time.
Please note that a cover letter is required as part of the application. The cover letter should explain your interest in this opportunity and how it aligns with your career goals. Applications missing this document will not be considered.
Cedars-Sinai has an outstanding opportunity for an independent and well-organized contributor to serve as a CLINICAL RESEARCH ASSOCIATE II to Dr. Judy Tan to support community-engaged research that develops behavioral and community-based health interventions for LGBTQ+ communities of color. Dr. Tan, Associate Professor, Cancer Research Center for Health Equity, Division of Population Sciences, Department of Biomedical Sciences, is a social psychologist and applies her training in behavioral and prevention sciences to develop innovative interventions for improving health outcomes among marginalized populations in the U.S.
This position provides contributions to behavioral and implementation science for the Cancer Research Center for Health Equity. The scope of the work includes research involving participants recruited from the surrounding LA communities and interactions with community-based researchers, academic researchers, and local community organizations and health systems.
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 coordinate and/or implement increasingly complex research studies. Supports objectives of research studies through noncomplex tasks such as data collection, prescreening of potential and scheduling of current research participants, assisting in IRB submission activities, budget and billing, and ensuring overall compliance with all federal and local guidelines. Provides increasingly complex and independent support for studies by serving as the independent contact with sponsors, IRB, and research participants, providing training, education to junior level staff, and coordination of ad hoc activities related to studies. May serve independently as study coordinator for minimal number of noncomplex research studies or projects.
Responsibilities:
  • Works independently under minimal direction from a Clinical Research Coordinator, Research Program Administrator, Research Nurse, or other supervising staff to coordinate and/or implement increasingly complex research studies.
  • Collects, evaluates and/or abstracts clinical research data. May assist in designing forms for data collection/abstraction. Enters and processes clinical research data into Electronic Data Systems (EDCs) that are provided by the sponsors.
  • Completes Case Report Forms (CRFs).
  • Independently prescreens potential research participants for various clinical trials. Schedules research participants for research visits and research procedures. May provide increasingly independent contact with research participants and/or conduct research participant visits independently.
  • Assists supervising staff with regulatory submissions to the Institutional Review Board (IRB). May work directly with the Institutional Review Board to submit Adverse Events, Serious Adverse Events, Safety Letters, etc in accordance with local and federal guidelines.
  • Assists with clinical trial budgets and patient billing.
  • Responsible for sample preparation and shipping and maintenance of study supplies and kits.
  • Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with all federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board. Maintains research practices using Good Clinical Practice (GCP) guidelines. Maintains strict patient confidentiality according to HIPAA regulations and applicable law.
  • May serve as the primary point of contact for external sponsors for select trials. Responds to sponsor inquiries and attends meetings regarding study activities.
  • Participates in and provides training and education to other Clinical Research Associates. May assist in coordinating activities of other associates to ensure compliance with protocol and clinical research objectives.
  • Participates in centralized activities such as auditing, Standard Operating Procedure development, etc.
  • May participate in the development of Investigator Initiated trials for Investigational New Drug applications and/or Device applications
  • May provide coordination of minimal number of noncomplex research studies or projects independently. May provide coverage for study coordination activities of supervising staff when needed to ensure minimal disruption to study objectives.

Qualifications
Education
  • High School Diploma/GED - minimum
  • Bachelor's Degree Science, Sociology or related degree. - preferred

Experience
  • 1 year Clinical research related. - minimum

Licenses and Certifications
  • Certification In Clinical Research - preferred SOCRA or ACRP certification

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