How your CV stacks up
Upload your CV to see how well it fits this job role
?%
FutureMeds: Shaping the Future of Clinical Research
Join us and become part of a team dedicated to excellence, collaboration, and the transformation of patient care through innovative research.
Position Overview
We are looking for a proactive and detail-oriented Study Coordinator to join the team at our busy and well established Liverpool site. In this key role, you will play an integral part in our clinical studies by maintaining meticulous documentation and strict adherence to protocols. You will ensure all records are kept to a high standard, helping to keep the site audit ready at all times.
The ideal candidate will have previous experience in a data entry or data management role, with experience in a clinical research investigator site being advantageous but not essential. We are keen to hear from candidates who are new to the industry and can demonstrate relevant transferable skills. The successful candidate will be organised, able to meet strict deadlines, and flexible in their approach to adapting and reprioritising tasks. This role is based fully on site in our Wirral clinic.
Reasons to use Rodeo
Start with a chat, not a search bar
Grad scheme, placement, apprenticeship? Not sure what you want yet — that's fine. Your agent talks it through with you and turns "I have no idea" into a shortlist.
It searches the market for you
Every day your agent scans the market matching roles against what actually matters to you, not just keywords on a CV.
Only hits
No noise. No "maybe this fits." Just roles with a clear explanation of why they're right — and where to focus when applying.
Key Responsibilities
- Ensure accurate collection, entry, and maintenance of clinical trial data
- Monitor data consistency, completeness, and adherence to study protocols
- Ensure all study deadlines are met
- Collaborate with relevant teams to ensure quality and integrity of all study data
- Always ensure the strictest confidence and adherence to GDPR guidelines
- Maintain records to ensure that the site remains audit ready at all times
- Assist with preparation for internal and external audits and inspections, and contribute as required
- Prepare data summaries and reports as required
- Work closely with colleagues and sponsors to ensure seamless data flow
- Support communication between teams to address data queries promptly
- Ensure high-quality data is available at all times
- Work closely and provide support to site clinical and administration teams
- Communicate with clients by phone or email
- Booking and rescheduling of monitor visits as required
- Ensure prompt and accurate communication with sponsors and CRA’s
- Communicate effectively and provide data as requested by the Site Director
- Contribute to meetings with study sponsors/CROs, site clinical or full team meetings
Get help with your application
Your very own career expert that helps elevate your application to the next level.
Qualifications and Skills
- Previous experience in a data entry or management role is preferable.
- Experience in a clinical research environment is beneficial.
- Strong attention to detail and accuracy in data entry and record-keeping.
- Excellent communication skills, both written and verbal.
- Ability to prioritise tasks and manage time effectively to meet deadlines.
- Proactive problem-solving skills and a collaborative approach to working with cross-functional teams.
Benefits
- Competitive salary package
- Comprehensive benefits package including pension, life assurance, private healthcare, and bonus
- Potential for career progression and growth
- A dynamic working environment that celebrates success and rewards initiative
- The chance to be part of making a meaningful contribution to the advancement of clinical research and healthcare
“It took my CV and asked me questions relevant to understanding what kind of jobs to suggest for me. Suggestions were almost perfect. Jobs were exactly what I’ve been looking for.”
Jessica, London
Skills
Location