Remote quality assurance pharmaceutical Work, Jobs (with Salaries)

Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance programme
Regulatory Affairs Consultant - CMC vax/bio (home or office based)
Parexel —Remote
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Microsoft Excel
IP Support Specialist (Renewals)
Reddie & Grose LLP —London
- Microsoft Outlook
- English
- Microsoft Office
- Annual leave
- Employee assistance programme
Finance Business Partner - Enabling Functions
Dechra Pharmaceuticals PLC —Remote
- £75,000 - £80,000 a year
- Remote
- Master's degree
- Bachelor's degree
- Travel
- Employee assistance programme
Laboratory Support - DMPK
Charles River Laboratories —Saffron Walden
- Weekend availability
- Sales
- Laboratory experience
- Communication skills
- Paid training
- Annual leave
Business Analyst
SkyCell AG —London
- Full-time
- Remote
- Computer Science
- Bachelor's degree
- APIs
- Annual leave
- Flexible schedule
Quick apply
QA Auditor
hVIVO Services Limited —London
- In-person
- Communication skills
13d
Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting
IQVIA —Reading
- Full-time
- Hybrid work
- Doctoral degree
- Master's degree
- Leadership
Senior QA Auditor (GCP)
hVIVO Services Limited —London
- In-person
- Communication skills
13d
Legal Advisor
General Pharmaceutical Council —London
- £55,000 - £62,000 a year
- Full-time
- Hybrid work
- Communication skills
Head of Product - Digital Channels & Platform
Dechra Pharmaceuticals PLC —Remote
- £90,000 - £95,000 a year
- Remote
- Travel
- APIs
- Employee assistance programme
Digital Advanced Clinical Practitioner
Doctor Care Anywhere —London
- £60,169 a year
- Part-time
- Remote
- Master's degree
- IT
- Communication skills
- Annual leave
Quick apply
Head of Clinical Genetics (Maternity cover - 12 months)
Sano Genetics —London
- £80,000 - £90,000 a month
- Remote
- Doctoral degree
- Data analysis skills
- Laboratory experience
Regional IT Manager – England North
Teledyne Technologies Inc. —Lincoln
- Full-time
- CAD
- Windows
- IT
- Annual leave
- Employee assistance programme
GCP Compliance Director (EMEA Hub)
Novartis —London
- £83,510 - £155,090 a year
- Full-time
- Hybrid work
- Mentoring
- Leadership
1d
Performance Test Consultants
Eurofins UK Edge Testing Solutions —London
- Full-time
- DevOps
Quick apply
Survey Programmer (contractor)
Kielo Research —Remote
- Remote
- Microsoft Powerpoint
- Computer Science
- Analysis skills
Quick apply
Account Manager
Lumanity —Remote
- Hybrid work
- Project management
- Bachelor's degree
- Travel
- Annual leave
11h
Adult ADHD Clinical Nurse Specialist
South London and Maudsley NHS Foundation Trust —London
- £58,133 - £65,261 a year
- Full-time
- Leadership
- Communication skills
1d
Senior Telesales Executive
PHSGroup —Laleham
- £35,000 a year
- No weekends
- Sales
- Salesforce
- Microsoft Office
- Free parking

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Clinical Research Associate (CRA)

Aspire Pharma Ltd
Remote

Apply Now

Job details

Permanent

Benefits

Cycle to work scheme
Company pension
Company events
Employee assistance programme
Private medical insurance

Qualifications

Microsoft Word
Microsoft Excel
Microsoft Outlook
Microsoft Office
Organisational skills
Document management systems
Communication skills
Adobe Acrobat
Time management

Full job description

Competitive Salary & Company Benefits| Remote or Hybrid Working
Monday to Friday, 9.00am - 5.00pm (potential for flexibility on start/end times based on 7.5hrs/day).

Are you looking to work for a rapidly growing UK Pharmaceutical company, who are passionate about improving patients' lives across the world?

Aspire Pharma is an asset-light pharmaceutical manufacturer. It licenses and develops niche pharmaceutical products that offer innovative formulations, value for money for payors, and reliable supply arrangements in markets which are often underserved. The business has a highly diversified portfolio of more than 250 products across a number of categories, including branded specialty products and unbranded niche generics in therapeutic areas such as urology, ophthalmology, CNS and dermatology.

Do you want to be part of the journey?
If so, here is your chance!

The Role

We are currently looking to recruit a Clinical Research Associate (CRA). The CRA provides essential operational and administrative support to the delivery of clinical trials and bioequivalence studies. This role plays a key part in ensuring studies are conducted efficiently, on time, and in compliance with ICH GCP, Aspire SOPs, and applicable regulatory requirements.

The CRA is responsible for maintaining high-quality, inspection-ready documentation, supporting study coordination activities, and enabling effective collaboration across cross-functional teams, vendors, and external partners.

This is a hands-on role suited to a detail-oriented professional who thrives in a fast-paced, regulated environment.

Technical Skills

Proficient in Microsoft Office (Word, Excel, Outlook)
Experience with electronic document management systems (e.g., eTMF)
Familiarity with clinical trial management systems (CTMS) is desirable
Experience with Adobe Acrobat and electronic signature tools

Professional Qualification & Experience

Degree in Life Sciences subject or a related field
Typically, 5-10 yearsâ€™ experience in clinical operations within the pharmaceutical or CRO industry
Experience supporting clinical trials and/or bioequivalence studies
Experience working in a GCP-regulated environment
Experience working with a sponsor organisation is desirable
Experience in a virtual or outsourced operating model is advantageous

Knowledge, Skills, & Competencies

Strong understanding of ICH GCP and applicable regulatory requirements (EMA/FDA desirable)
High attention to detail with a strong focus on quality and compliance
Excellent organisational and time management skills
Strong written and verbal communication skills
Ability to work collaboratively in cross-functional and global teams
Proactive approach to problem-solving and risk identification
Ability to manage multiple priorities in a fast-paced environment

Study Coordination & Support

Support the day-to-day running of clinical trials and bioequivalence studies
Oversee all aspects of trial management, be the main point of contact for internal and external stakeholders, and actively support audits/inspections
Assist project teams in planning, tracking, and delivering study milestones
Assist in the preparation and review of study protocols, informed consent forms and study reports
Identify and escalate risks or issues that may impact study delivery

Documentation & Compliance

Set up, maintain, and ensure completeness of Trial Master Files (TMF) and sponsor oversight files (electronic and/or paper) in accordance with clinical trial requirements
Ensure all study documentation is accurate, up-to-date, and inspection-ready
Perform quality control checks on clinical trial documentation
Track key document milestones to ensure ongoing regulatory compliance
Support audit and inspection readiness activities, including resolution of findings

Systems & Tracking

Maintain and update clinical trial tracking systems (e.g., CTMS, trackers)
Ensure accurate recording of study progress, documentation status, and key metrics
Support data integrity and consistency across systems

Meeting & Vendor Coordination

Coordinate clinical trial meetings, including scheduling, logistics, and preparation of materials
Prepare and distribute meeting agendas and minutes
Support communication and coordination with CROs, vendors, and study sites

Regulatory & External Activities

Support posting and maintenance of study information on external platforms (e.g., ClinicalTrials.gov)
Assist with preparation and distribution of study documentation to sites
Collaborate with Regulatory, Quality, and Pharmacovigilance teams to ensure compliance

Cross-functional Collaboration

Work closely with R&D, Regulatory Affairs, Quality, Pharmacovigilance, and other stakeholders
Support internal and external project managers in study-related activities
Contribute to process improvements and operational efficiency initiatives

General Support

Provide broader administrative support to the R&D function as required
Support additional clinical operations activities in line with business needs

Why Join Us?

As well as a fantastic, inclusive company culture, where employees are truly valued, and a competitive salary, we also offer an ever-improving benefits scheme to support your physical and mental well-being which include:

Company pension scheme.
Life Assurance cover and Employee Assistance Program.
25 days' holiday plus bank holidays.
Learning and development opportunities.
Excellent opportunities for progression.
Fantastic company events and celebrations throughout the year.
Cycle to Work Scheme
Private healthcare schemes

Work Location: Remote

Apply Now

Refine Your Search

remote quality assurance pharmaceutical jobs

Clinical Research Associate (CRA)

Regulatory Affairs Consultant - CMC vax/bio (home or office based)

IP Support Specialist (Renewals)

Finance Business Partner - Enabling Functions

Laboratory Support - DMPK

Business Analyst

QA Auditor

Associate Principal / Principal, Clinical Outcome Assessment (COA) Strategy Consulting

Senior QA Auditor (GCP)

Legal Advisor

Head of Product - Digital Channels & Platform

Digital Advanced Clinical Practitioner

Head of Clinical Genetics (Maternity cover - 12 months)

Regional IT Manager – England North

GCP Compliance Director (EMEA Hub)

Performance Test Consultants

Survey Programmer (contractor)

Account Manager

Adult ADHD Clinical Nurse Specialist

Senior Telesales Executive

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