At a Glance
- Tasks: Monitor clinical trials, ensure compliance, and build strong relationships with clients and site teams.
- Company: Join PHARMExcel, a leading CRO dedicated to high-quality clinical services.
- Benefits: Competitive salary, generous leave, private medical insurance, and remote-first culture.
- Why this job: Make a real impact in clinical research while working with top professionals in the field.
- Qualifications: 2-3+ years CRA experience, oncology knowledge, and a degree in life sciences.
- Other info: Supportive team environment with opportunities for personal and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
As an ISO 9001 certified organisation, PHARMExcel prides itself in delivering high quality and results driven clinical services. Our broad portfolio ranges from non-interventional, CTIMP, ATMP, rare disease and medical devices investigations. You will be working with key opinion leaders, world class academics and entrepreneurs across the biotech and medtech sectors.
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.
You will:
- 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
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, must have oncology experience 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
- 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
- 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
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.
Ready to make a difference? Apply today and be part of something exceptional at PHARMExcel!
Clinical Research Associate II (CRA II) in Welwyn Garden City employer: PHARMExcel Ltd
Contact Detail:
PHARMExcel Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Associate II (CRA II) in Welwyn Garden City
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who work at PHARMExcel or similar companies. A friendly chat can lead to insider info about job openings and even referrals.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of ICH-GCP and ISO 14155. Be ready to discuss your experience with multi-centre trials and how you’ve tackled challenges in previous roles. Show them you’re the CRA II they need!
✨Tip Number 3
Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation. It keeps you fresh in their minds and shows your enthusiasm for the role.
✨Tip Number 4
Apply through our website for the best chance of landing that CRA II position. It’s the most direct route to getting noticed by our hiring team. Plus, it shows you’re genuinely interested in being part of the PHARMExcel family!
We think you need these skills to ace Clinical Research Associate II (CRA II) in Welwyn Garden City
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the CRA II role. Highlight your relevant experience in monitoring multi-centre clinical trials, especially in oncology. We want to see how your skills align with what we’re looking for!
Showcase Your Attention to Detail: In your application, emphasise your meticulous nature and problem-solving skills. Mention specific examples where you ensured compliance and maintained high-quality documentation. This is key for us at PHARMExcel!
Craft a Compelling Cover Letter: Your cover letter should reflect your passion for clinical research and your collaborative spirit. Share why you want to join our team and how you can contribute to our supportive culture. We love hearing your story!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining PHARMExcel!
How to prepare for a job interview at PHARMExcel Ltd
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of ICH-GCP and ISO 14155 standards. Being able to discuss these regulations confidently will show that you're serious about compliance and quality in clinical trials.
✨Showcase Your Problem-Solving Skills
Prepare examples from your past experiences where you've successfully navigated challenges in clinical trials. Highlighting your ability to find solutions and manage risks will resonate well with the interviewers.
✨Demonstrate Your Team Spirit
Since PHARMExcel values collaboration, be ready to share instances where you've worked effectively within a team. Emphasise your positive attitude and willingness to support others, as this aligns with their company culture.
✨Prepare for Scenario-Based Questions
Expect questions that put you in hypothetical situations related to site monitoring or compliance issues. Practising your responses to these scenarios will help you articulate your thought process and decision-making skills during the interview.