Clinical Research Assistant jobs
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- You have successfully managed multiple clinical trial protocols across diverse investigative sites.
- IQVIA has access to significant data pools allowing better…
Clinical Research Nurse
NewOften replies in 3 daysResearch LinkLeicestershire- Free parking
- On-site parking
- Previous experience of clinical research in wound care.
- Understanding of current relevant clinical and professional issues.
- Pay: £37,315.00-£39,191.00 per year.
- Good knowledge of, and skill in applying, applicable clinical research regulatory requirements i.e., Good Clinical Practice (GCP) and International Conference…
View similar jobs with this employerIQVIAOxfordshire- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Senior Clinical Research Coordinator
Often replies in 1 dayThe Bodyline Clinic LimitedStoke-on-Trent ST1 5SJ- Employee discount
- Significant experience within clinical research laboratories.
- Bodyline Medical Wellness Clinics is a leading CQC-registered clinical services and clinical…
- VitalographMaids Moreton
- Annual leave
- Company pension
- Generous time off – 23 days of annual leave to recharge and unwind.
- Document control, to include study-specific and general documentation.
View similar jobs with this employerIQVIAChesterfield- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
Project Coordinator
NewOften replies in 1 dayActivinsights LtdHuntingdon PE28 0LF- Life insurance
- Free parking
- Private dental insurance
- Company pension
- Private medical insurance
- Company events
- A scientific or clinical background is beneficial but not essential.
- Working closely with the Data Manager, you will help ensure the successful planning,…
Project Coordinator
NewOften replies in 1 dayActivinsights LtdHuntingdon PE28 0LF- Life insurance
- Free parking
- Private dental insurance
- Company pension
- Private medical insurance
- Company events
- A scientific or clinical background is beneficial but not essential.
- Working closely with the Data Manager, you will help ensure the successful planning,…
- PLE Health LtdStroud GL5 3EW
- Free parking
- Company pension
- Casual dress
- On-site parking
- To carry out routine clinical administration tasks related to cases including but not limited to:
- Assist in conducting a clinical audit of outcome measures for…
Clinical Research Nurse
NewOften replies in 4 daysPanthera BiopartnersYork YO24 4LJ- Annual leave
- Employee discount
- Sick pay
- Life insurance
- Company pension
- Private medical insurance
- You will work alongside the wider clinical research team in the assessment and management of patient care pathways.
- Monday to Friday (No evenings or Weekends).
Job Post Details
Clinical Research Associate - job post
Job details
Job type
- Full-time
Location
Full job description
IQVIA's Site Management (multi-sponsor) team are seeking a Clinical Research Associate to join us on our mission to help create a healthier world.
The Clinical Research Associate will support Oncology studies and cover sites across the UK
Apply today and forge a career with greater purpose, make an impact and never stop learning!
Responsibilities
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability.
- Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.
- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase.
- Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements.
- Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
- Collaborate and liaise with study team members for project execution support as appropriate.
Requirements
-
Experience of independent on-site monitoring of Oncology therapeutic area for unblinded studies.
-
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
-
Life science degree educated or equivalent industry experience
-
Flexibility to travel to sites as required
*Please note - this role is not eligible for visa sponsorship*
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 https://jobs.iqvia.com
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.