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.
About FutureMeds
FutureMeds is a network of modern dedicated research sites conducting clinical trials. We find eligible patients for trials across a wide variety of therapy areas, helping pharmaceutical companies and contract research organisations to run clinical trials as efficiently and cost effectively as possible. Our priority is the safety and health of our patients and by helping to bring them future medicines today we can play a key part in improving health.
Position Overview
We are looking for a proactive and detail-oriented Study Coordinator to join the team at our busy Birmingham 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, keeping the site audit ready at all times.
The ideal candidate will bring prior experience as a Study Coordinator within a clinical research investigator site, with a comprehensive understanding of clinical trials and study protocols. Adept at meeting strict deadlines and possessing the flexibility to adapt and reprioritise tasks in a fast-paced environment. This is an exciting opportunity for an experienced Study Coordinator with a passion for clinical research, who is eager to take on a new role within an already thriving site. This role is based fully on-site at our Birmingham clinic.
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 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
Qualifications and Skills
- Experience as a Study Coordinator within a clinical research environment.
- Experience in a commercial healthcare setting preferable.
- 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
- 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
Job Types: Full-time, Permanent
Application question(s):
- Will you now, or in the future, require visa sponsorship?
Experience:
- Clinical Research: 2 years (required)
- Study Coordinator: 2 years (required)
Work authorisation:
- United Kingdom (required)
Work Location: In person
