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

Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
- Referral programme
3d
Remote Pilot Specialist
Skyports Limited —Aylesbury
- £35,000 - £45,000 a year
- Full-time
- Hybrid work
- Up to 50% travel
- Travel
Quick apply
Sr. Specialist, Regulatory Affairs
The Bountiful Company —Tring
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Quick apply
Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
3d
Senior Specialist Regulatory Affairs
Abbott Laboratories —Witney
- Full-time
- Maintenance
- Bachelor's degree
- Communication skills
8d
EMEA Regulatory Affairs Specialist - Cosmetics
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
11d
Quality Assurance Specialist
Oxford Nanopore Technologies —Oxford
- Full-time
- Bachelor's degree
- Organisational skills
- SharePoint
4d
Senior Regulatory Specialist
UK Atomic Energy Authority —Culham
- £71,815 a year
- Full-time
- Engineering
- Annual leave
- Employee assistance programme
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Clinical Trial Assistant - Clinical Supplies
ICON Plc —Reading
- Full-time
- Remote
- Data analysis skills
- Bachelor's degree
- Communication skills
- Employee assistance programme
9d
Pharmacy Quality Assurance and Control Assistant
Oxford University Hospitals NHS Foundation Trust —Oxford
- £25,760 - £27,476 a year
- Full-time
1d
Regulatory Development Specialist
UK Atomic Energy Authority —Culham
- £57,117 a year
- Full-time
- Engineering
- Travel
- Annual leave
- Employee assistance programme
Continuous Improvement & Innovation Specialist
PerkinElmer —Seer Green
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
(Fixed Term) Data Quality Control Specialist. Clinical Biomarker Laboratory
Moderna, Inc. —Oxford
- Full-time
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Annual leave
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
10d
Senior Project Specialist, Clinical Supplies
Moderna, Inc. —Oxford
- Full-time
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Outlook
- Annual leave
6d
Specialist, Content Producer
Pearson —Oxford
1d
Specialist Biomedical Scientist (x2)
Deciphex —Oxford
- 8 hour shift
- Laboratory experience
- Mentoring
- Annual leave
Quick apply
Compliance Manager (Regulatory Compliance)
AVK —Maidenhead
- £50,000 - £60,000 a year
- Full-time
- Hybrid work
- Communication skills
Quick apply
Lead Theatre Practitioner
Circle Health Group —Great Missenden
- Up to £50,000 a year
- Full-time
- Hospital
- Travel
- Mentoring
- Employee discount
- Life insurance

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regulatory specialist jobs near thame, oxf

Regulatory and Start Up Specialist - UK

IQVIA -
Reading

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Job details

Full-time
3 days 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 thame, oxf

Regulatory and Start Up Specialist - UK

Remote Pilot Specialist

Sr. Specialist, Regulatory Affairs

Regulatory Affairs Specialist

Senior Specialist Regulatory Affairs

EMEA Regulatory Affairs Specialist - Cosmetics

Quality Assurance Specialist

Senior Regulatory Specialist

Senior Regulatory Affairs Specialist

Clinical Trial Assistant - Clinical Supplies

Pharmacy Quality Assurance and Control Assistant

Regulatory Development Specialist

Continuous Improvement & Innovation Specialist

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

Quality Improvement Lead

Senior Project Specialist, Clinical Supplies

Specialist, Content Producer

Specialist Biomedical Scientist (x2)

Compliance Manager (Regulatory Compliance)

Lead Theatre Practitioner

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