Clinical research associate ii, oncology Work, Jobs in Oadby, Lec (with Salaries)

Clinical Research Associate
IQVIA —Nottingham
- Full-time
- No degree
- Travel
Macmillan Skin Cancer Clinical Nurse Specialist
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Organisational skills
- Communication skills
2d
Clinical Specialist Sonographer, ENT Ultrasound (B8A or B7 Trainee)
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £64,750 a year
- Weekend availability
1d
Consultant Gynaecologist- Specialist Interest Gynae Oncology
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £113,565 - £150,569 a year
- Full-time
8d
Locum Consultant in Medical Microbiology
Nottingham University Hospitals NHS Trust —Nottingham
- £109,725 - £145,478 a year
- Full-time
7d
Gynaecology Oncology CNS and CSPL
George Eliot Hospital NHS Trust —Nuneaton
- £49,387 - £56,515 a year
- Full-time
- Annual leave
- Referral programme
6d
Oncology Breast Cancer Clinical Nurse Specialist
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Maintenance
- Organisational skills
- Leadership
6d
3D Digital Biomedical Engineer
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
6d
Bank Chemotherapy Nurse
Spire Healthcare —Leicester
- Weekend availability
- Hospital
- Patient care
- Communication skills
- Free parking
- Annual leave
13d
Specialist Oncology Dietitian
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £39,959 - £48,117 a year
- Full-time
- Teaching
- Flexible schedule
7d
Oncology Support Secretary
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £25,760 - £27,476 a year
- Full-time
2d
Specialist Pharmacist Clinical Trials
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Project management
2d
Specialist Nurse - Cancer Services (12 Months Fixed Term)
Spire Healthcare —Leicester
- Full-time
- Management
- Annual leave
Specialist Pharmacist Clinical Trials (Experienced)
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £49,387 - £56,515 a year
- Full-time
- Project management
4d
Oncology Specialist Nurse- Part Time- Immunotherapy
Apodi ltd —Nottingham
- From £45,000 a year
- Part-time
- Anatomy knowledge
- Medication administration
- Hospital
Quick apply
Locum Consultant
Pro Medicus Ltd —Nuneaton
- £95 - £110 an hour
- Temporary
- Anatomy knowledge
- Medication administration
- Hospital
Quick apply
2d
Locum Consultant in Emergency Medicine
University Hospitals Coventry and Warwickshire NHS Trust —Coventry
- £113,565 - £150,569 a year
- Part-time
5d
Paediatric Team Leader Dietitian
Nottingham University Hospitals NHS Trust —Nottingham
- £49,387 - £56,515 a year
- Full-time
- University
- Leadership
- Communication skills
8d
Specialist Chemotherapy Nurse
Sciensus —Nottingham
- From £40,500 a year
- Care plans
- Annual leave
- Employee discount
Quick apply
Registered Nurse – Oncology/Haematology (Bank)
Circle Health Group —Nottingham
- Up to £23 an hour
- Part-time
- Hospital
- Care plans
- Communication skills
- Annual leave

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Clinical Research Associate

IQVIA -
Nottingham

Apply Now

Job details

Full-time

Qualifications

Project implementation

Full job description

Nottingham, United Kingdom | Full time | Field-based | R1514135

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.

Apply Now

Refine Your Search

clinical research associate ii, oncology jobs in oadby, lec

Clinical Research Associate

Macmillan Skin Cancer Clinical Nurse Specialist

Clinical Specialist Sonographer, ENT Ultrasound (B8A or B7 Trainee)

Consultant Gynaecologist- Specialist Interest Gynae Oncology

Locum Consultant in Medical Microbiology

Gynaecology Oncology CNS and CSPL

Oncology Breast Cancer Clinical Nurse Specialist

3D Digital Biomedical Engineer

Bank Chemotherapy Nurse

Specialist Oncology Dietitian

Oncology Support Secretary

Specialist Pharmacist Clinical Trials

Specialist Nurse - Cancer Services (12 Months Fixed Term)

Specialist Pharmacist Clinical Trials (Experienced)

Oncology Specialist Nurse- Part Time- Immunotherapy

Locum Consultant

Locum Consultant in Emergency Medicine

Paediatric Team Leader Dietitian

Specialist Chemotherapy Nurse

Registered Nurse – Oncology/Haematology (Bank)

I want to receive the latest job alerts for clinical research associate ii, oncology in oadby, lec

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