At a Glance
- Tasks: Monitor clinical trials, ensure compliance, and support site teams in delivering excellence.
- Company: Join PHARMExcel, a growing CRO that values integrity and teamwork.
- Benefits: Competitive salary, car allowance, generous leave, and private medical insurance.
- Other info: Flexible working, learning opportunities, and a culture that values your voice.
- Why this job: Make a real impact in clinical research while working remotely with a supportive team.
- Qualifications: 2-3+ years CRA experience and a degree in life sciences or related field.
The predicted salary is between 35000 - 45000 £ per year.
Location: UK
Role Type: Remote
Salary: Competitive salary + car allowance & benefits
Start Date: July-September 2026
Contract Type: Full time
Travel: UK sites with potential global travel in future.
About the role
As a CRA II at PHARMExcel, you will play a pivotal role in supporting our clients, sites, and clinical project team. You will be the key point of contact for site liaison, ensuring integrity, compliance, and excellence in every phase of trial delivery. You will be comfortable with problem solving, finding solutions, risk management and have meticulous attention to detail. Excellent report writing and compliance with timelines will be expected. You will be part of a supportive and welcoming team that is all about helping each other grow. We are looking for someone who will bring that same positive, collaborative spirit to the role.
- Monitor multi-centre, clinical trials across various therapeutics and phases
- Build strong relationships with our clients, investigators, and site teams
- Ensure compliance with GCP, ICH, ISO 14155, and regulatory standards
- Contribute to ethics and regulatory submissions
- Maintain high-quality documentation and oversee source data verification
This is a remote role with quarterly in-person team days at our Head Office in Welwyn Garden City and travel to trial sites as required. Site travel is required around every 6-8 weeks.
Key responsibilities
- Site selection, set-up, initiation, monitoring, and close-out
- Deliver study-specific training at Site Initiation Visits (SIVs)
- Manage case report form (CRF) data accuracy and source data verification (SDV)
- Track subject recruitment progress and ensure site compliance
- Prepare visit reports, follow-up letters, and monitoring documentation
- Escalate protocol violations and serious breaches in a timely manner
- Collaborate with eTMF specialists, CRAs, and project managers to maintain trial quality
- Participate in SOP updates, process improvement, and team development
About you
We are looking for someone who is meticulous, proactive, and collaborative—with a strong desire to make an impact in clinical research. You will bring:
- 2–3+ years’ CRA experience (at CRA I or II) monitoring multi‑centre clinical trials preferably early phase.
- Demonstrated breadth of experience across Phase I to IV
- Degree in a life sciences or related field
- Strong working knowledge of ICH‑GCP
- Excellent communication and people skills
- Strong presentation skills (verbal & written)
- Ability to travel as required
- Organised, self‑driven, and able to manage multiple priorities
Must have
- Right to work in UK
- Driving licence – clean
- Passport
- Energy and passion
- Integrity and desire to learn
Nice to have
- Familiarity with ISO 14155 and medical device regulations
- Sense of humour and team spirit
What you will receive
- Competitive salary (DOE) & car allowance
- Generous annual leave + your birthday off
- Private medical insurance
- Company bonus (performance‑based)
- Remote‑first culture with flexible working
- Learning & development opportunities
- Family‑friendly policies & travel incentives
- Professional memberships paid for
- 24/7 confidential Employee Assistance Programme (EAP)
- Wellbeing, ESG, and charity initiatives
- Supportive and collaborative work culture
Why PHARMExcel?
We are a growing CRO that values integrity, teamwork, and passion. You will be part of a company that invests in its people and provides opportunities to make a real difference in the world of clinical research. Here, your voice is heard. Your work is valued. And your growth is supported.
PHARMExcel is an equal opportunities employer and does not discriminate on the grounds of gender, sexual orientation, marital or civil partner status, pregnancy or maternity, gender reassignment, race, colour, nationality, ethnic or national origin, religion or belief, disability or age. Our ethos is to respect and value people’s differences, and to help everyone achieve and be their best at work as well as in their personal lives so that they feel proud of the part they play in our success. We believe that all decisions about people at work should be based on the individual’s abilities, skills, performance and behaviour and our business requirements. PHARMExcel operates a zero‑tolerance policy to any form of discrimination, abuse or harassment.
Clinical Research Associate II (CRA II) in Welwyn Garden City employer: Meeveem Limited
PHARMExcel is an exceptional employer that prioritises integrity, teamwork, and personal growth within the clinical research field. With a remote-first culture, competitive salary, generous benefits, and a strong commitment to employee development, you will thrive in a supportive environment that values your contributions and encourages collaboration. Located in Welwyn Garden City, easily accessible by train and road, PHARMExcel offers a unique opportunity to make a meaningful impact while enjoying a balanced work-life experience.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Research Associate II (CRA II) in Welwyn Garden City
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We think you need these skills to ace Clinical Research Associate II (CRA II) in Welwyn Garden City
Some tips for your application 🫡
Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at Meeveem Limited!
Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show Meeveem Limited that you're not just a fit for the job but also a safety-conscious candidate!
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How to prepare for a job interview at Meeveem Limited
✨Understand the Science
Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at Meeveem Limited that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.
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If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.
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In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.
