Regulatory specialist Work, Jobs in Tadley, Ham (with Salaries)

Regulatory and Start Up Specialist - UK
IQVIA —Reading
- Full-time
- Remote
- Maintenance
- Bachelor's degree
5d
EMEA Regulatory Affairs Specialist - Cosmetics
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
13d
VodafoneThree - PMO Specialist
Vodafone —Newbury
- Full-time
- Hybrid work
- Employee discount
22h
Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
6d
VodafoneThree - Quality Radio Performance Specialist
Vodafone —Newbury
- Full-time
- Hybrid work
- Data analysis skills
- Analysis skills
- Communication skills
- Employee discount
5d
Arrears & Collections Associate
Castle Trust Bank —Basingstoke
- £28,000 - £32,000 a year
- Full-time
- Hybrid work
- Customer service
- Microsoft Office
- Communication skills
- Employee assistance programme
- Employee discount
Quick apply
Senior Regulatory Affairs Specialist
Kenvue —Reading
- Hybrid work
- English
- Bachelor's degree
- Organisational skills
- Annual leave
Team Leader
Mears Group —Basingstoke
- Up to £40,000 a year
- Monday to Friday
- Microsoft Excel
- Microsoft Office
- Analysis skills
- Annual leave
- Employee assistance programme
3d
Compliance Specialist
Estee Lauder —Petersfield
- Microsoft Office
Customer Success Onboarding Specialist (12 Month Contract)
Geotab —Reading
- Hybrid work
- Analysis skills
- Bachelor's degree
- Continuous improvement
Specialist, GPV Performance Excellence - Monitoring Team (18-month FTC)
Kyowa Kirin International —Marlow
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
Sr. Payroll Specialist | Reading-based | Polish or Czech speaking
OpenText —Reading
- Tax experience
VodafoneThree - Data Governance and Quality Lead
Vodafone —Newbury
- Full-time
- Hybrid work
- Employee discount
6d
Systems Audit Specialist
Surrey Police —Guildford
- £39,149 - £45,058 a year
- Weekend availability
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
- Annual leave
- Employee discount
8d
Early Careers Lead
Stantec —Reading
- Project management
- Organisational skills
- IT
- Annual leave
Sr Quality Specialist
IQVIA —Reading
- Full-time
- Hybrid work
- Bachelor's degree
- Travel
Chief Technology Officer - Connected Medical Technology
Neupulse —Basingstoke
Quick apply
4d
Safeguarding and Complex Health Lead
Montu UK —Winnersh
- £57,500 - £62,500 a year
- Full-time
- Hybrid work
- Case management
- Travel
- Organisational skills
Project Manager, Remote Research Clinicians
IQVIA —Reading
- Full-time
- English
- Project management
- Bachelor's degree
Data Logger Operative (Maintenance) - South East Water - SWAP Candidate Only
Tetra Tech —Basingstoke
- Weekend availability
- Hybrid work
- Schematics
- Microsoft Office
- Administrative experience
10d

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regulatory specialist jobs near tadley, ham

Regulatory and Start Up Specialist - UK

IQVIA -
Reading

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Job details

Full-time
5 days ago

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.

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 tadley, ham

Regulatory and Start Up Specialist - UK

EMEA Regulatory Affairs Specialist - Cosmetics

VodafoneThree - PMO Specialist

Regulatory Affairs Specialist

VodafoneThree - Quality Radio Performance Specialist

Arrears & Collections Associate

Senior Regulatory Affairs Specialist

Team Leader

Compliance Specialist

Customer Success Onboarding Specialist (12 Month Contract)

Specialist, GPV Performance Excellence - Monitoring Team (18-month FTC)

Sr. Payroll Specialist | Reading-based | Polish or Czech speaking

VodafoneThree - Data Governance and Quality Lead

Systems Audit Specialist

Early Careers Lead

Sr Quality Specialist

Chief Technology Officer - Connected Medical Technology

Safeguarding and Complex Health Lead

Project Manager, Remote Research Clinicians

Data Logger Operative (Maintenance) - South East Water - SWAP Candidate Only

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