Clinical trial Work, Jobs in Remote (with Salaries)

Clinical Research Associate (CRA)
Aspire Pharma Ltd —Remote
- Monday to Friday
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
- Employee assistance programme
7d
Medical Doctor (UK) - Freelance AI Trainer Project
Meridial —Remote
- £40 - £120 an hour
- Remote
- AI
- Annual leave
Country Approval Specialist - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Bachelor's degree
- Organisational skills
Project Manager, Clinical Trials
Cogstate —Remote
- £55,000 - £60,000 a year
- Remote
- Computer Science
- Engineering
- Master's degree
- Annual leave
Quick apply
Clinical Development Scientist - Biosimilars
Advanz Pharma —Remote
- Remote
- Doctoral degree
- Master's degree
- Employee assistance programme
Medicine Specialist (Fluent in German) - Freelance AI Trainer Project
Meridial —Remote
- £8 - £65 an hour
- Remote
- Doctoral degree
- Engineering
- Master's degree
- Annual leave
Sr/CRA I/II - UK (numerous locations)
Thermo Fisher Scientific —Remote
- Full-time
- English
- Microsoft Office
- Presentation skills
Learning Experience Designer & Academy Builder
Life Balance Chiropractic —Remote
- £24 - £60 an hour
- Part-time
- Remote
- Care plans
Quick apply
14d
Principal Statistician Oncology with Submission Experience
Syneos - Clinical and Corporate - Prod —Remote
- Full-time
- Remote
- English
- Travel
- Contracts
Consultant - Clinical Operations (Remote - Europe)
Veeva Systems —Remote
- Full-time
- Remote
- Spanish
- Computer Science
- English
- Annual leave
- Work from home
Research Fellow
Plymouth University —Remote
- £39,906 - £46,049 a year
- University
- In-person
- Annual leave
- Employee assistance programme
6d
Project Manager
Endpoint Clinical —Remote
- £45,000 - £50,000 a year
- Full-time
- Remote
- Customer service
- SQL
- Project management
Project Manager
Catalyst Clinical Research, LLC —Remote
- Full-time
- Remote
- Microsoft Office
- Analysis skills
- Project management
Senior Regulatory Affairs Associate
Simbec-Orion —Remote
- Full-time
- Remote
- Doctoral degree
- English
- Master's degree
11d
Contract Specialist - FSP
Thermo Fisher Scientific —Remote
- 8 hour shift
- Remote
- English
- Organisational skills
- Contracts
Business Analyst
AARK TECH SOLUTIONS GmbH —Remote
- Remote
- Azure
- Analysis skills
- APIs
Senior Medical Science Liaison, Solid Tumours - United Kingdom
BeiGene —Remote
- £80,000 - £100,000 a year
- Full-time
- CRM software
- Doctoral degree
- English
CTM/Sr CTM - EMEA - FSP
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- English
- Project management
- Bachelor's degree
Senior/Principal Clinical Team Manager - Internal Medicine
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Microsoft Outlook
- English
- Bachelor's degree
Safety Scientist- Real World Evidence (RWE), EMEA
Thermo Fisher Scientific —Remote
- Full-time
- Remote
- Data analysis skills
- Machine learning
- Travel

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Clinical Research Associate (CRA)

Aspire Pharma Ltd
Remote

Apply Now

Job details

Permanent
7 days ago

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 trial jobs in remote

Clinical Research Associate (CRA)

Medical Doctor (UK) - Freelance AI Trainer Project

Country Approval Specialist - FSP

Project Manager, Clinical Trials

Clinical Development Scientist - Biosimilars

Medicine Specialist (Fluent in German) - Freelance AI Trainer Project

Sr/CRA I/II - UK (numerous locations)

Learning Experience Designer & Academy Builder

Principal Statistician Oncology with Submission Experience

Consultant - Clinical Operations (Remote - Europe)

Research Fellow

Project Manager

Project Manager

Senior Regulatory Affairs Associate

Contract Specialist - FSP

Business Analyst

Senior Medical Science Liaison, Solid Tumours - United Kingdom

CTM/Sr CTM - EMEA - FSP

Senior/Principal Clinical Team Manager - Internal Medicine

Safety Scientist- Real World Evidence (RWE), EMEA

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