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Clinical Research Ii Jobs (NOW HIRING)

Washington University of St. Louis

$54K - $81K/yr

As a Clinical Research Coordinator II, you will work alongside our team of highly skilled research coordinators and clinicians in executing clinical trial protocols for pediatric patients with ...

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Clinical Research Ii information

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$49K

$107.3K

$189K

How much do clinical research ii jobs pay per year?

As of Aug 10, 2026, the average yearly pay for clinical research ii in the United States is $107,336.00, according to ZipRecruiter salary data. Most workers in this role earn between $81,000.00 and $122,500.00 per year, depending on experience, location, and employer.

What is the difference between Clinical Research Ii vs Clinical Research Coordinator?

AspectClinical Research IiClinical Research Coordinator
Required CredentialsBachelor's degree, often in life sciences; some roles may require certificationBachelor's degree; certification like CCRP is a plus
Work EnvironmentResearch sites, hospitals, pharmaceutical companiesResearch sites, hospitals, clinics
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research organizations
Common Search & ComparisonOften compared for entry-level research rolesOften compared for site-based research management

Clinical Research Ii and Clinical Research Coordinator roles share similar environments and educational requirements. However, Clinical Research Ii typically involves more data management and protocol adherence, while Clinical Research Coordinators focus on patient interaction and site coordination. Both roles are essential in clinical trials, but they differ in daily responsibilities and focus areas.

What are some common challenges faced by Clinical Research II professionals, and how can they be managed?

Clinical Research II professionals often encounter challenges such as balancing multiple studies simultaneously, ensuring protocol compliance, and managing regulatory documentation. Effective time management and strong organizational skills are essential for handling these demands. Additionally, frequent communication with both internal teams and external sites helps to resolve issues quickly and maintain study timelines. Leveraging digital tools for tracking progress and staying updated with regulatory changes can also streamline daily responsibilities and reduce stress.

What is a Clinical Research II?

A Clinical Research II is a mid-level professional involved in the planning, coordination, and execution of clinical research studies. They typically have experience in clinical research and may oversee study protocols, manage data collection, and ensure compliance with regulatory standards. Clinical Research II professionals often serve as a liaison between study sites, sponsors, and regulatory bodies, and may mentor junior staff. They play a key role in ensuring the quality and integrity of clinical trials to support medical advancements.

What are the key skills and qualifications needed to thrive as a Clinical Research II?

To excel as a Clinical Research II professional, you need a strong background in clinical trial management, regulatory compliance, and data analysis, often supported by a degree in life sciences or a related field. Familiarity with tools such as electronic data capture systems (e.g., REDCap), Good Clinical Practice (GCP) certification, and clinical trial management software is typically required. Outstanding attention to detail, problem-solving abilities, and effective communication help manage complex studies and collaborate with stakeholders. These skills are essential to ensure accurate data collection, regulatory adherence, and successful study outcomes.
More about Clinical Research Ii jobs
What job categories do people searching Clinical Research Ii jobs look for? The top searched job categories for Clinical Research Ii jobs are:
Clinical Research Ii jobs near you
Infographic showing various Clinical Research Ii job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $107,336 per year, or $51.6 per hour.

Clinical Research Data & Regulatory Coordinator

Mary Bird Perkins Cancer Center

Baton Rouge, LA • On-site

$23.25 - $31/hr

Full-time

Posted 22 days ago

Mary Bird Perkins Cancer Center rating

7.6

Company rating: 7.6 out of 10

Based on 5 frontline employees who took The Breakroom Quiz

Job description

Mary Bird Perkins Cancer Center is Louisiana's leading cancer care organization, caring for more patients each year than any other facility in the region. And with strategic hospital and physician partnerships, we are delivering on our mission to improve survivorship and lessen the burden of cancer.
Mary Bird Perkins and its partners work together to provide state-of-the-art treatments and unparalleled collaborative, comprehensive cancer services. This culture of innovation helps attract the best cancer minds in the country, from expert physicians and highly specialized scientists to forward-thinking leaders in supportive care and other disciplines.
Together, with our hospital and physician partners, we are one-hundred percent focused on cancer care.
Why Join Us? We are looking for talented and highly-motivated individuals who demonstrate a natural desire to support the meaningful work of community oncologists and the patients we serve.
Job Description:
100% IN PERSON POSITION
SCOPE: The Data and Regulatory Coordinator collaborates with the Clinical Research team and the Principal Investigator by knowledge of current protocol requirements; maintains IRB documents, regulatory and protocol documentation for assigned clinical trials administered by the Center which may include multi-site trials; facilitates communication and correspondence between Clinical Research and sponsoring agencies; collects protocol specific information from physicians, nurses, patients, family members, local caregivers, and others utilizing protocol specific methods; ensures that all designated Clinical Research regulatory and data management activities for all clinical research sites are executed in accordance with all applicable laws, regulations, policies and protocol requirements; performs additional duties as requested by supervisor and/or described in position description.
ESSENTIAL FUNCTIONS:
1. Demonstrates knowledge and understanding of the evolution of clinical research.
2. Participates in clinical research studies by assuring that the regulatory and data for trials being managed according to rules and guidelines governing the conduct of clinical research trials.
3. Monitor/Auditor Preparation and Participation
4. IRB Preparation and Presentation
5. Protocol research document maintenance
6. Policies & procedures
7. Other duties and professional development
QUALIFICATIONS:
  • Bachelor's degree or equivalent work experience, preferably in a scientific or technical discipline.
  • Basic science degree, or certification or licensure in a health care field
  • Demonstrated success in management of regulatory submissions activities.
  • Medical or scientific research experience preferred.
  • Professional Certifications preferred

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