Research Assistant Health jobs
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.
- Degree in scientific discipline / health care or equivalent industry experience.
- Well‑being support covering your physical, mental, and financial health.
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
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.
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.
- Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and Good Clinical Practice.
- IQVIA has access to significant data pools allowing better site selection and recruitment.
- Perform site monitoring visits (selection, initiation, monitoring and…
Research Physician
Often replies in 1 dayThe Bodyline Clinic LimitedOpenshaw- As the successful role holder you will play a pivotal part in delivering high-quality clinical research across a range of therapeutic areas, with a strong focus…
Clinical Research Nurse
NewOften replies in 3 daysResearch LinkLeicestershire- Free parking
- On-site parking
- Previous experience of clinical research in wound care.
- Clinical research: 1 year (required).
- Involvement with the running of several concurrent research…
- Degree in scientific discipline / health care or equivalent industry experience.
- Well‑being support covering your physical, mental, and financial health.
- Degree in scientific discipline / health care or equivalent industry experience.
- Well‑being support covering your physical, mental, and financial health.
- Degree in scientific discipline / health care or equivalent industry experience.
- Well‑being support covering your physical, mental, and financial health.
Research Associate
Often replies in 1 dayiCan Wellbeing Group CIOCarlisle CA2 5SR- Flexitime
- Gym membership
- Free fitness classes
- Company pension
- On-site gym
- On-site parking
- The post holder will provide research training, research awareness campaigns, data management and research administrative support, as needed for all projects…
- GBS UKLondon
- Referral programme
- Annual leave
- Employee discount
- Company pension
- Cycle to work scheme
- Tech scheme
- Previous experience of working in the health industry as a health practitioner.
- Previous training experience to large groups about health related subjects.
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.
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.