Clinical Research Coordinator Greater Manchester
- Recruiter
- IQVIA CSMS
- Location
- Lancashire
- Salary
- Competitive
- Posted
- 01 Jul 2022
- Closes
- 08 Jul 2022
- Sectors
- Scientific & Pharmaceutical
- Contract Type
- Permanent
- Hours
- Full Time
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.
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.