At a Glance
- Tasks: Manage clinical sites, ensure compliance, and support study recruitment.
- Company: Leading clinical research organisation with a focus on innovation.
- Benefits: Competitive salary, flexible hours, and opportunities for professional growth.
- Other info: Fast-paced environment with a strong emphasis on teamwork and development.
- Why this job: Join a dynamic team and contribute to groundbreaking medical research.
- Qualifications: Bachelor's degree in a relevant field and 8+ years of CRA experience.
The predicted salary is between 54000 - 66000 £ per year.
Responsibilities
- (a) Site management
- Study site selection, initiation (SIV) and clinical monitoring.
- Perform pre-study visit to ensure eligible sites are selected according to sponsor site selection criteria, including but not limited to adequate resources and experience.
- Prepare and conduct SIV to ensure adequate study training for relevant site staff to proceed with study start and conduct in compliance with protocol and relevant regulations.
- Ensure Principal Investigator/study staff complies with safety reporting requirements, as defined in protocol, SOP, ICH-GCP and GCP.
- Track study recruitment to ensure recruitment target is achieved in all studies.
- Conduct monitoring visit according to SDV plan and SOP; address issues with sites and complete monitoring visit report in a timely manner coordinating.
- Ensure timely coordination of study materials (drug, non-drug, equipments, CRFs) to the site for start-up and throughout the study.
- Assemble site specific EC submission dossier, and ensure submission to EC.
- Training
- Provide ongoing training to site staff with regards to ICH-GCP, GCP, study protocol and requirements.
- Conduct site initiation to ensure that the site has a thorough understanding of the study protocol and requirements.
- Documentation
- Ensure timely collection of essential documents in compliance with protocol and regulations at study start-up, during and at study close-down.
Maintain and update these documents in investigator files, trial master files.
- Prepare/complete study records’ archiving according to protocol and sponsor requirements.
- (b) Drug Safety
- Ensure safety information is disseminated to all sites according SOP and applicable regulations.
- Ensure SAE is reported within the timeline in compliance with SOPs and applicable regulations.
- (c) Finance and Administration
- Finalize budget and obtain signed contract from site, prior to site initiation visit.
- Ensure Study Payment Schedule is executed and retain relevant documents/receipts.
- (d) Study Tools and system
- Update and maintain Study tools/systems in a timely manner.
- 3. Qualifications
3.1 Bachelor degree or above in Medical, Pharmacology or Biology related major.
3.2 At least 8 year of CRA experience;
3.3 Good understanding and knowledge of Good Clinical Practice and clinical trial operation processes/procedures;
3.4 Good skills on Microsoft Word, Excel, PPT and Outlook, etc.
Contractor CRA_UK employer: Tigermed
As a Contractor CRA in the UK, you will join a dynamic team that values collaboration and professional growth. Our company offers a supportive work culture with ongoing training opportunities, ensuring you stay at the forefront of clinical research practices. With a focus on employee well-being and a commitment to excellence, we provide a rewarding environment where your contributions directly impact the success of clinical trials.
