Research Nurse
Location: South London
Weekly working hours: 30h
Start Date: May 2026
Duration: 2 years
IQVIA is seeking an experienced Clinical Research Nurse to support a clinical research site in South London Brixton. This 30h per week role offers the opportunity to contribute to high-quality clinical trial within a collaborative research environment. The role will be supporting an opioid use disorder trial.
Key Responsibilities
- Support patient screening recruitment and enrollment including informed consent and pre-consent activities
- Collect medical and concomitant medication history
- Perform and document vital signs (including height and weight) and ECGs
- Provide administrative support for AE/SAE documentation and reporting per protocol and regulatory requirements
- Manage Investigational Product (IP): receipt storage accountability preparation dispensing administration and return/destruction
- Collect process and ship laboratory samples
- Enter verify and correct source data in CRFs EDC eCOA and other study systems; manage data queries
- Maintain the Investigator Site File including IRB/IEC submissions and communications
- Use IVRS/IXRS and other trial-related systems
- Coordinate patient scheduling and provide ongoing participant support
- Support recruitment initiatives referrals and community/physician outreach
- Perform general study-related administrative tasks including EMR printing and certification
Required Qualifications & Experience
- Nursing qualification with current RN registration
- Experience working in Mental Health/Addiction/Substance Abuse
- Minimum 2 years experience as a Research Nurse in clinical trials
- Strong knowledge of clinical trial conduct protocols consent processes and medical terminology
- Proven experience with IP handling ECGs vital signs and laboratory procedures
- Proficiency in MS Office and clinical trial systems
- Excellent communication organizational skills and attention to detail
Why IQVIA
Join a global leader in clinical research and healthcare innovation. At IQVIA youll work on impactful studies in a supportive and professional environment.
Interested
Apply today to be part of meaningful clinical research with IQVIA.
#LI-HCPN
#LI-CES
#LI-DNP
#LI-NS1
#LI-Onsite
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
Required Experience:
IC
Research NurseLocation: South LondonWeekly working hours: 30hStart Date: May 2026Duration: 2 yearsIQVIA is seeking an experienced Clinical Research Nurse to support a clinical research site in South London Brixton. This 30h per week role offers the opportunity to contribute to high-quality clinical ...
Research Nurse
Location: South London
Weekly working hours: 30h
Start Date: May 2026
Duration: 2 years
IQVIA is seeking an experienced Clinical Research Nurse to support a clinical research site in South London Brixton. This 30h per week role offers the opportunity to contribute to high-quality clinical trial within a collaborative research environment. The role will be supporting an opioid use disorder trial.
Key Responsibilities
- Support patient screening recruitment and enrollment including informed consent and pre-consent activities
- Collect medical and concomitant medication history
- Perform and document vital signs (including height and weight) and ECGs
- Provide administrative support for AE/SAE documentation and reporting per protocol and regulatory requirements
- Manage Investigational Product (IP): receipt storage accountability preparation dispensing administration and return/destruction
- Collect process and ship laboratory samples
- Enter verify and correct source data in CRFs EDC eCOA and other study systems; manage data queries
- Maintain the Investigator Site File including IRB/IEC submissions and communications
- Use IVRS/IXRS and other trial-related systems
- Coordinate patient scheduling and provide ongoing participant support
- Support recruitment initiatives referrals and community/physician outreach
- Perform general study-related administrative tasks including EMR printing and certification
Required Qualifications & Experience
- Nursing qualification with current RN registration
- Experience working in Mental Health/Addiction/Substance Abuse
- Minimum 2 years experience as a Research Nurse in clinical trials
- Strong knowledge of clinical trial conduct protocols consent processes and medical terminology
- Proven experience with IP handling ECGs vital signs and laboratory procedures
- Proficiency in MS Office and clinical trial systems
- Excellent communication organizational skills and attention to detail
Why IQVIA
Join a global leader in clinical research and healthcare innovation. At IQVIA youll work on impactful studies in a supportive and professional environment.
Interested
Apply today to be part of meaningful clinical research with IQVIA.
#LI-HCPN
#LI-CES
#LI-DNP
#LI-NS1
#LI-Onsite
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.
Required Experience:
IC
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