Regulatory specialist Work, Jobs in Chilton, Oxf (with Salaries)

Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
- Referral programme
17h
Senior Regulatory Specialist
UK Atomic Energy Authority —Culham
- £71,815 a year
- Full-time
- Engineering
- Annual leave
- Employee assistance programme
Senior Specialist Regulatory Affairs
Abbott Laboratories —Witney
- Full-time
- Maintenance
- Bachelor's degree
- Communication skills
5d
Regulatory Development Specialist
UK Atomic Energy Authority —Culham
- £57,117 a year
- Full-time
- Engineering
- Travel
- Annual leave
- Employee assistance programme
Remote Pilot Specialist
Skyports Limited —Aylesbury
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Up to 50% travel
- Travel
Quick apply
Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
1d
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
EMEA Regulatory Affairs Specialist - Cosmetics
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
8d
Financial Crime Senior Investigator
Nationwide Building Society —Swindon
- From £32,800 a year
- Full-time
- Communication skills
- Time management
6d
Procurement Officer
UK Research and Innovation (UKRI) —Harwell
- £37,841 a year
- Full-time
- Hybrid work
- English
- IT
- Annual leave
- Employee assistance programme
13d
Quality Improvement Lead
Principal Medical Limited —Bicester
- £50,000 - £55,000 a year
- Full-time
- Microsoft Word
- Management
- Microsoft Office
- Free parking
- Sick pay
Quick apply
8d
Research Facilitator
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £32,073 - £39,043 a year
- Part-time
12d
ECC Operations Manager
Nationwide Building Society —Swindon
- £64,000 - £70,000 a year
- Full-time
- IT
6d
Compliance Manager (Regulatory Compliance)
AVK —Maidenhead
- £50,000 - £60,000 a year
- Full-time
- Hybrid work
- Communication skills
Quick apply
DICE Lab Manager
UK Atomic Energy Authority —Abingdon
- £57,117 a year
- Full-time
- Engineering
- Supervising experience
- Organisational skills
- Annual leave
- Employee assistance programme
Quick apply
Quality Systems Specialist
Oxford Nanopore Technologies —Oxford
- Full-time
- Bachelor's degree
- Organisational skills
- SharePoint
1d
Senior Project Specialist, Clinical Supplies
Moderna, Inc. —Oxford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Annual leave
4d
(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory
Moderna, Inc. —Oxford
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
VodafoneThree - Quality Radio Performance Specialist
Vodafone —Newbury
- Full-time
- Hybrid work
- Data analysis skills
- Analysis skills
- Communication skills
- Employee discount
21h
Operations Director Medicine Division
Hampshire Hospitals NHS Foundation Trust —Basingstoke
- £112,782 - £129,783 a year
- Full-time
9d

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regulatory specialist jobs near chilton, oxf

Regulatory and Start Up Specialist - UK

IQVIA -
Reading

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Job details

Full-time
17 hours ago

Benefits

Referral programme

Qualifications

Clinical research
Maintenance
Bachelor's degree

Full job description

Reading, United Kingdom | Full time | Home-based | R1552306

Job Overview
Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.

Home Based opportunity requiring experience with local submissions and contracts.

Essential Functions

Under general supervision, serve as Single Point of Contact (SPOC) in assigned studies for investigative sites, Site Activation Manager (SAM), Project Management team, and other departments as necessary.
Ensure adherence to standard operating procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines.
Perform start up and site activation activities according to applicable regulations, SOPs and work instructions.
Distribute completed documents to sites and internal project team members.
Prepare site regulatory documents, reviewing for completeness and accuracy.
Ensure accurate completion and maintenance of internal systems, databases and tracking tools with project specific information.
Review and provide feedback to management on site performance metrics.
Review, establish and agree on project planning and project timelines.
Ensure monitoring measures are in place and implement contingency plan as needed.
Inform team members of completion of regulatory and contractual documents for individual sites.
Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed Consent Form (ICF), and Investigator Pack (IP) release documents, in line with project timelines.
Provide local expertise to SAMs and project team during initial and on-going project timeline planning.
Perform quality control of documents provided by sites.
May have direct contact with sponsors on specific initiatives.

Qualifications
Bachelor’s Degree in life sciences or a related field and 3 years’ clinical research or other relevant experience; or equivalent combination of education, training and experience.

In-depth knowledge of clinical systems, procedures, and corporate standards.
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines.
Knowledge of applicable regulatory requirements, including local regulations, SOPs and company’s Corporate Standards.
Understanding of regulated clinical trial environment and knowledge of drug development process.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.

In today’s world, continuing to grow and expand your skills is as important as ever. Discover career possibilities and chart your own path at IQVIA.

The potential base pay range for this role, when annualized, is 33, 700 GBP - 61, 400 GBP. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

Employee Referral Payment

Standard Referral Bonus Plan

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

regulatory specialist jobs in chilton, oxf

Regulatory and Start Up Specialist - UK

Senior Regulatory Specialist

Senior Specialist Regulatory Affairs

Regulatory Development Specialist

Remote Pilot Specialist

Regulatory Affairs Specialist

Senior Regulatory Affairs Specialist

EMEA Regulatory Affairs Specialist - Cosmetics

Financial Crime Senior Investigator

Procurement Officer

Quality Improvement Lead

Research Facilitator

ECC Operations Manager

Compliance Manager (Regulatory Compliance)

DICE Lab Manager

Quality Systems Specialist

Senior Project Specialist, Clinical Supplies

(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory

VodafoneThree - Quality Radio Performance Specialist

Operations Director Medicine Division

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