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Clinical Research Associate Ii Jobs (NOW HIRING)

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Clinical Research Associate

Tampa, FL · On-site

$71K - $189K/yr

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Clinical Research Associate II & Senior Clinical Research Associate (CRA II/Sr. CRA) Multiple Therapeutic Areas | Nationwide Opportunities IQVIA is actively seeking experienced Clinical Research ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

Clinical Research Associate II Working at Abbott At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have ...

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

As the Clinical Research Associate II, you will assist in the clinical execution and management of assigned clinical studies. This includes but is not limited to planning and implementation of ...

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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 Sep 1, 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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Infographic showing various Clinical Research Associate Ii job openings in the United States as of August 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

Bio-Rad Laboratories

Seattle, WA • On-site

$83K - $114K/yr

Full-time

Medical, Life, Retirement, PTO

Re-posted 10 days ago


Bio-Rad Laboratories rating

7.0

Company rating: 7.0 out of 10

Based on 25 frontline employees who took The Breakroom Quiz

74th of 102 rated chemical manufacturers


Job description

Overview

As the Clinical Research Associate II, you will be responsible for planning, execution and oversight of clinical studies in compliance with ICH-GCP and IVD clinical guidelines, applicable regulatory requirements, and company SOPs. This role participates in the management of clinical study budgets and timelines. This role represents Clinical Affairs collaborates cross-functionally with Regulatory Affairs, R&D, Quality, Marketing, and external partners to deliver high-quality clinical data and evidence supporting product registration and commercialization of Bio-Rad diagnostic products. 

How You'll Make An Impact: 

  • Manage Clinical Studies required for the establishment of the performance of an IVD product. 
  • Authors clinical performance study monitoring plan, protocol, ICF, etc. in compliance with applicable regulations and standards. 
  • Selects, qualifies and onboards clinical study sites with the execution of study agreements and IRB approvals. 
  • Fosters effective communication and collaboration with study sites and/or CROs, and oversights the study execution from study site initiation, to site closeout. 
  • Monitors study progress, enrollment, data integrity, risk management, and ensure compliance with GCP and regulatory requirements.   

What You Bring: 

  • Education: Bachelor's degree in Life Sciences, Biomedical Sciences, or related field (advanced degree preferred). 
  • Work Experience: 2 years' experience in clinical research (clinical trials execution role, preferably in an IVD, device or pharma company). 
  • Experiences of using eTMF and EDC platforms during clinical research. 
  • Deep knowledge of FDA clinical research regulations, and ICH-GCP, ISO 13485, ISO 20916. 
  • Excellent written and effective verbal communication skills, and people management experience.

Location: This position must be based in Seattle, Washington and requires the employee to be located within commuting distance of the office.

Total Rewards Package: At Bio-Rad, we're empowered by our purpose and recognize that our employees are as well. That's why we offer a competitive and comprehensive Total Rewards Program that provides value, quality, and inclusivity while satisfying the diverse needs of our evolving workforce. Bio-Rad's robust offerings serve to enrich the overall health, wealth, and wellbeing of our employees and their families through the various stages of an employee's work and life cycle.

Benefits: We're proud to offer a variety of options, including competitive medical plans for you and your family, free HSA funds, a new fertility offering with stipend, group life and disability,  paid parental leave, 401k plus profit sharing, an employee stock purchase program, a new upgraded and streamlined mental health platform, extensive learning and development opportunities, education benefits, student debt relief program, pet insurance, wellness challenges and support, paid time off, Employee Resource Groups (ERG's), and more! 

Compensation: The estimated base salary range for this position is $83,000 to $114,200 at the time of posting. Actual compensation will be provided in writing at the time of offer, if applicable, and is based on several factors we believe fairly and accurately impact compensation, including geographic location, experience, knowledge, skills, abilities, and other job permitted factors. This position is eligible for a variable annual bonus, which is dependent upon achievement of your individual objectives and Company performance.

Who We Are: For 70 years, Bio-Rad has focused on advancing the discovery process and transforming the fields of science and healthcare. As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products. We help people everywhere live longer, healthier lives. Bio-Rad offers a unique employee experience with collaborative teams that span the globe. Here, you are supported by leadership to build your career and are empowered to drive change that makes an impact you can see.  

EEO Statement: Bio-Rad is an Equal Employment Opportunity/Affirmative Action employer, and we welcome candidates of all backgrounds. Veterans, people with physical or mental disabilities, and people of all race, color, sex, sexual orientation, gender identity, religion, national origin and citizenship status are encouraged to apply.

Agency Non-Solicitation:Bio-Rad does not accept agency resumes, unless the agency has been authorized by a Bio-Rad Recruiting Representative. Please do not submit resumes unless authorized to do so. Bio-Rad will not pay for any fees related to unsolicited resumes.

Fraud Alert: Bio-Rad has received reports of individuals posing as Bio-Rad recruiters to obtain information, including personal and financial, from applicants. Beware of these fake "recruiters" and job scams. Click here for more information on this scam and how to avoid it.  #LI-AK1

Employment Type: FULL_TIME

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