Clinical Research Coordinator Greater Manchester

Clinical Research Coordinator

Monday – Friday,37.5 hours/week, initial 3 month contract

Generous basic salary + comprehensive, fully customizable benefits package to suit you.

Are you looking for your next opportunity in Clinical Research?  Do you want to work for an industry leading company?  If so, come and join us - IQVIA are currently looking for 6 experienced site-based Clinical Research Coordinators in the following locations:

Preston (1 site)

Greater Manchester (2 sites)

Wakefield (1 site)

N London (2 sites)

Cornwall (2 sites)

For this project, we are looking for candidates who have:

• At least 1 year of clinical research experience
• Spent at least 1 year using relevant data management platforms (such as Medidata, RAVE etc.)
• A patient data driven approach, with experience in database lock or data cleaning (ideally with 1 milestone/database cleaning managed)
• Previous experience of EDC entry and query resolution
• Strong IT competence (including MS Windows and Office applications such as Access, Outlook, Excel, and Word)
• Dynamic, flexible, and adaptable in the changing clinical environment
• Reliable, with good teamworking, communication and collaboration skills.

Day to day responsibilities will include:

• Providing clinical research support to investigators to prepare for and execute assigned research studies, including: Review study protocols, Case Report Forms (CRFs), other study-specific documents, and electronic data capture systems used to record clinical research data
• Attending all relevant study meetings
• Collecting and submitting regulatory/ethics documentation as required by relevant regulatory bodies governing the conduct of clinical research
• Recruiting and screening patients for clinical trials and maintain subject screening logs
• Orienting research subjects to the study, including the purpose of the study, procedures, and protocol issues such as timelines for visits
• Designing and maintaining source documentation based on protocol requirements
• Scheduling and executing study visits and performing study procedures
• Collecting, recording and maintaining research subject study data according to study protocol and SOPs, preserving quality control for content, accuracy and completeness
• Handling lab testing and analysis, including preparation of specimen collection tubes and lab logistics
• Monitoring subject safety and reporting adverse reactions to appropriate medical personnel
• Corresponding with research subjects and troubleshoot study-related questions or issues
• Assisting with study data quality checking and query resolution
• Performing a variety of complex clinical research procedures including but not limited to ECG, sample collection, spirometry, vital signs, dose verification, cannulation and cardiac telemetry monitoring
• Recording, reporting and interpreting study findings appropriately to develop a study-specific database
• Assisting investigator in verifying that research study objectives are met on time, within budget and according to applicable protocol requirements, clinical research regulations and quality standards
• Assisting in maintaining adherence to investigator site staff training requirements by auditing and maintaining training records
• Preparing for and attending study monitoring visits, study audits, and regulatory inspections with clinical research regulatory agencies
• Assisting research site with coverage planning related to staffing and scheduling for research projects.

IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at https://jobs.iqvia.com