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Full Time Clinical Trial Rn Jobs (NOW HIRING)

Novant Health

Clinical Research Coordinator RN

Wilmington, NC · On-site

$59K - $74K/yr

What We Offer RNs with experience working in Oncology OR Clinical Research! This position offers ... Clinical Research Coordinators facilitate and coordinate daily clinical trial activities and play a ...

City of Hope

Clinical Research Nurse-Lymphoma

Duarte, CA · On-site

Are you a compassionate and detail-oriented Registered Nurse passionate about advancing healthcare? ... What You'll Do Clinical Trial Patient Management * Partner with investigators to determine patient ...

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Full Time Clinical Trial Rn information

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How much do full time clinical trial rn jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for full time clinical trial rn in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Full Time Clinical Trial Rn vs Clinical Research Coordinator?

AspectFull Time Clinical Trial RnClinical Research Coordinator
CredentialsRegistered Nurse (RN) license, clinical trial trainingBachelor's degree, research training, sometimes certification
Work EnvironmentHospitals, clinics, research sites, hospitalsResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, research organizations, hospitalsResearch institutions, hospitals, CROs
Job FocusPatient care, administering trial protocols, data collectionStudy coordination, patient recruitment, data management

While both roles are vital in clinical research, a Full Time Clinical Trial RN primarily provides patient care and ensures protocol adherence from a nursing perspective. In contrast, a Clinical Research Coordinator manages study logistics, patient recruitment, and data collection. Both roles often collaborate but differ in their core responsibilities and required credentials.

What cities are hiring for Full Time Clinical Trial Rn jobs? Cities with the most Full Time Clinical Trial Rn job openings:
What are the most commonly searched types of Clinical Trial Rn jobs? The most popular types of Clinical Trial Rn jobs are:
What states have the most Full Time Clinical Trial Rn jobs? States with the most job openings for Full Time Clinical Trial Rn jobs include:
Full Time Clinical Trial Rn jobs near you

Senior Clinical Trial Case Manager

CSL

King Of Prussia, PA

Full-time

Posted 19 days ago

Job description

The Role:

  • Acts as Case Management subject matter expert in cross-functional teams for assigned clinical trials.

  • Manages case management activities for assigned clinical studies to ensure compliance with national and international regulations, such as GxP guidelines and/or other relevant international and national legislation, regulations, guidance, and company policies and procedures within the area of responsibility.

  • Manages the delivery of the Safety Reporting Plans, ; identifies, implements, and monitors KPIs/KQIs across clinical case management activities;

  • Supports the preparation and conduct of PV and other GxP inspections and audits, as required, .

  • Establishes, maintains, and/or ensures maintenance of clinical trial case management required documents, such as safety reporting plans and reporting responsibilities , in line with international and national regulations, guidelines, and internal standards.

  • Oversee the Vendors to ensure GSPV standards are maintained with respect to processing of SAE, AESI and pregnancy clinical trial cases and compliance with respect to expedited reporting in clinical trials.

  • Act as primary contact for external vendors for all GSPV PV Operations clinical trial queries pertaining to their assigned Clinical trials.

  • Prepare & Provide Study specific training to external vendors and GSPV team members involved in the given clinical trial.

  • Participate in any drug safety database enhancements and upgrades by providing input from a clinical trial perspective.

  • Develops, implements, and oversees pharmacovigilance procedures and processes and ensures the uniform and timely processing and analysis of safety data to comply with regulatory requirements.

  • Ensures correct coding of all event and drug terms.

  • Ensures inter- and intra-consistency for case evaluations.

  • Leads or oversees ICSR reporting compliance analyses provided by vendors and associated CAPAs from clinical trial case management.

  • Acts as a liaison internally and with external collaborators to develop processes that meet regulatory reporting requirements.

  • Oversees preparation of Suspected Unexpected Serious Adverse Reactions for submission to external regulatory agencies.

  • May lead or contribute to cross-functional projects to fulfill GxP requirements and improve inspection readiness.

Skills and Experience:

  • Bachelor's degree or equivalent in a life science discipline (e.g., nursing, biological sciences, pharmaceutical sciences, or Medical Documentation). Master's or PhD in Life Sciences preferred.

  • 7+ years of Pharmacovigilance experience in a multinational pharmaceutical industry environment.

  • Expert knowledge of local and international regulations and PV processes.

  • Knowledge of local and international GxP regulations, IT standards, and other relevant legislation, including privacy protection requirements.

  • Experience with regulatory inspections.

  • Experience administering complex data sets.

  • Experience managing CAPA and SOP development projects.

  • Experience with relevant software applications.

  • Experience working within a GxP-regulated environment.

Commonwealth Serum Laboratories logo

About Commonwealth Serum Laboratories

Sourced by ZipRecruiter

Commonwealth Serum Laboratories (CSL) is a global leader in biotechnology, based in King of Prussia, Pennsylvania. The company originates from Australia, founded in 1916 by the Australian government to service the country’s health needs. Since then, CSL has expanded operations to become a multinational specialty biotechnology company that researches, develops, and manufactures vaccines and plasma protein biotherapies. Their mission is underpinned by focused, patient-driven values. Our commitment to saving lives and protecting people's health by providing safe and effective products is a testament to the difference we are making. One of their considerate achievements includes establishing one of the largest influenza vaccine providers in the world through their brand Seqirus.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

King of Prussia, PA, US

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