Clinical trials associate 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
Clinical Research Associate
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
14d
Clinical Research Associate II
Parexel —Remote
- Remote
- Bachelor's degree
- Computer skills
- Communication skills
Associate (Clinical Outcome Assessments - COA)
Clarivate —London
- Full-time
- Hybrid work
- Microsoft Powerpoint
- Microsoft Office
- Master's degree
- Annual leave
- Gym membership
CRA2 - Multi-Sponsor Department
IQVIA —Reading
- Full-time
- Remote
- No degree
- Work from home
Clinical Trial Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
11d
Research Assistant/ Associate in Translational Cancer Research
Newcastle University —Newcastle upon Tyne
- £33,951 - £35,608 a year
- Full-time
- Doctoral degree
- Laboratory experience
- University
Research Associate
Cardiff University —Cardiff
- £41,064 - £46,049 a year
- Full-time
- Doctoral degree
- University
Senior Clinical Research Associate I
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
14d
Principal Statistician Oncology with Submission Experience
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- English
- Travel
- Contracts
Principal Statistical Programmer, SDTM and ADaM. Sponsor Dedicated
Syneos - Clinical and Corporate - Prod —Remote
- Part-time
- Remote
- English
- Bachelor's degree
- No degree
3d
Senior Clinical Research Associate II
Pfizer —Remote
- Weekend availability
- Nursing
- Patient monitoring
- English
14d
Drug Safety Associate II
Corbus Pharmaceuticals Inc —London
- Remote
- Microsoft Powerpoint
- Microsoft Word
- Nursing
Quick apply
Project Manager II (EU or UK Based)
Clinical Ink —Remote
- Remote
- Project management
- Bachelor's degree
- No degree
Quick apply
Clinical Trials Manager
Gilead Sciences —London
- Full-time
- Management
- Doctoral degree
- Master's degree
Research Associate
Newcastle University —Newcastle upon Tyne
- £36,636 - £46,049 a year
- Full-time
- Doctoral degree
- University
- IT
8d
Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection
IQVIA —Reading
- Full-time
- Remote
- English
- Microsoft Office
- Bachelor's degree
- Work from home
2d
Research Associate - Post stroke communication disorders
University of Sheffield —Sheffield
- £38,784 - £47,389 a year
- Part-time
- Hybrid work
- Google Suite
- Doctoral degree
- English
- Annual leave
- Employee discount
Associate Clinical Technologist
Cardiff and Vale University Health Board —Cardiff
- £28,819 - £31,626 a year
- Full-time
7d
Study Start Up Associate
ICON Plc —Reading
- Full-time
- Bachelor's degree
- Travel
- Organisational skills
- Employee assistance programme
8d

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Clinical Research Associate (CRA)

Aspire Pharma Ltd
Remote

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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

clinical trials associate jobs

Clinical Research Associate (CRA)

Clinical Research Associate

Clinical Research Associate II

Associate (Clinical Outcome Assessments - COA)

CRA2 - Multi-Sponsor Department

Clinical Trial Associate

Research Assistant/ Associate in Translational Cancer Research

Research Associate

Senior Clinical Research Associate I

Principal Statistician Oncology with Submission Experience

Principal Statistical Programmer, SDTM and ADaM. Sponsor Dedicated

Senior Clinical Research Associate II

Drug Safety Associate II

Project Manager II (EU or UK Based)

Clinical Trials Manager

Research Associate

Associate Director Quality - Client Dedicated- Regional Clinical Compliance Inspection

Research Associate - Post stroke communication disorders

Associate Clinical Technologist

Study Start Up Associate

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