Great opportunity to join this niche patient recruitment company, who provide services for accelerated patient identification globally. Working within a small and dynamic team this role would suite someone who is looking for a broad and varied role offering flexibility.
This role would offer the successful candidate to make contribution to reviewing and setting op processes and procedures as well as working with some world leading clients. This permanent role offers an excellent salary and flexible working conditions.
Provides logistics support to our client Trials team
Develops and maintains effective working relationships with team members, investigators and clients
Assists our client Trials' study teams with effective communication between all study team members
Tracks and manages the ordering and distribution supplies throughout the study.
Coordinates investigator and study team contacts and scheduled calls
Tracks and Maintains StudyInformation and Documentation and Reports on Study Recruitment
Maintains accurate tracking and reporting of progress in study recruitment
Oversees the timely tracking of patients recruitment and alerts study team of any delays or issues
Maintains^tools for recruitment of patients and ensures prompt update and delivery to investigator sites
Study File Management
Maintains and ensures the completeness of the relevant sections of the study file as appropriate
Identifies and contributes to areas of best practice and process improvements
Incorporates learning and recommendations from study debriefs and best practices.
Essential Skills & Qualification
Essential Skills & Qualifications Required
Good understanding of study tracking tools, particularly Excel
Excellent phone manner and good time management skills
Software Competence: MS Office, proficient in Excel
Valid Driving License: Not Required
Working Language(s): English
Requirement for Business Travel: No
Flexible Working Hours: Yes
Employer: Patient Recruitment
Employment Type: Permanent
Hours: Full time
Contract Term: N/A
Location: UK; Location, Office Based in Hertfordshire
Plan Start Date: ASAP
Please do not apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
Employer Benefits: Company Pension.
MS Office, Excel
Clinical Research,^Clinical Operations, Clinical R&D, CRA, CTM, CTA, GCP, Site Manager, Monitor, Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility , Essential Documents, GCP, SOPs, Compliance, Training, Investigator Meeting, REC, Research Ethics. R&D, Trust, SMO, Site Manager, Quality Control, QC, EDC
Clinical Trial Applications, CTA,
Budget, vendor, RFP, variation, scope, outsource, CRO selection, Contracts, Clinical Trial Agreements, C&O. Bids, Proposals,Negotiation, Accruals, Financial
Quality Assurance, Audit, Inspection, CAPA, Findings, CQA, GMP, GCP, Qualified Person, QP, Clinical QA, Auditor, GCP Inspection, PVG Inspection
PVG, Pharmacovigilance, Safety, Drug Safety, Triage, Case, Narratives, PSUR, ASR, SAEs, ADRs, Argus, Trackwise, MedDRA
Assigned Consultant: Matthew Pike at CSL Recruitment on 01932 234 685
Please feel free to call for a detailed Job Description or additional information
Applications are reviewed within^24hrs, applicants will only receive feedback if they demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request^that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate.