## Overview
DermEffects Research is a very busy Clinical Research Site in London. We specialize in conducting Phase I-IV clinical trials in dermatology.
## About the Role
We're looking for a Clinical Research Coordinator to support the successful execution of clinical studies by managing a mix of administrative and clinical tasks. In this role, you'll work closely with Investigators to ensure study activities are organised, compliant, and aligned with protocol requirements. The Clinical Research Coordinator brings strong attention to detail and a solid grasp of study protocols, helping keep research operations running smoothly, accurately and on time.
This is a full-time position
## Responsibilities
Study Coordination & Participant Safety
- Ensure the safety and well-being of all study participants
- Conduct study visits in line with the protocol, GCP, and Internal SOPs
- Collect study-specific assessments (e.g., vitals, ECGs, phlebotomy, etc.)and maintain documentation accuracy
- Obtain and maintain proper informed consent
- Receiving investigational products and supplies
- Lab Sample Processing and Shipping
Recruitment, Screening & Enrollment
- Promote and support recruitment initiatives to identify eligible study participants
- Screen participants according to protocol inclusion/exclusion criteria
- Guide participants through the consent process and ensure proper documentation
- schedule and coordinate study visits across the full lifecycle of participation
Study Execution & Data Collection
- Perform clinical tasks such as phlebotomy, sample processing/shipping, point-of-care testing , and participant monitoring
- accurately complete source documentation, CRF's queries, and maintain records
- Dispense and track investigational products according to protocol
- Collect and report adverse events, including timely SAE reporting
Quality, Compliance & Site Support
- Prepare for monitoring visits, audits and maintain regulatory files
- perform regular quality control checks on source data and documents
- support lab supply inventory, equipment maintenance, and administrative needs
## Experience
You Might Be a Great Fit If You:
- Prior experience as a Clinical Research Coordinator
- Strong analytical skills and attention to detail
- Proficiency in PS Suite EMR, Microsoft Office
- Excellent written and verbal communication skills in English
- Experienced with giving subcutaneous injections
- Have a Science/Health educational background (minimum college diploma), or research-related field (or equivalent combination of education and experience)
- Have 1-2 years of experience in a healthcare setting and are comfortable with clinical tools like blood pressure monitors, ECG machines, and weight scales
- Experience with phlebotomy
- Understand basic medical terminology, or are eager to learn it quickly
- Are passionate about contributing to clinical trials that impact global health
- Are organized, detailed-oriented,, and skilled at multitasking in a fast-paced environment
- Are proactive, collaborative, and take ownership of your work
- Value open communication and thrive in a team-driven environment
- Can work independently and as a team player
Job Type: Full-time
Pay: $23.00-$25.00 per hour
Benefits:
Education:
- AEC / DEP or Skilled Trade Certificate (preferred)
Experience:
- Clinical research: 2 years (preferred)
Language:
Work Location: In person
