Study Start up Manager, Contractor Required Now
My client has an immediate need for a capable study manager to help accelerate study start up on a new trial placed with a reputable CRO.
A regular role involving^all aspects of study management across functions including document review and approval, definition of work practices and tools, regulatory and biometric interactions and oversight of scope, budget and timelines. You will need to be capable of leading from Day 1 and not someone who need support and guidance, our client needs a proficient person who has managed CRO outsourced trials and ensured compliance and attention to the detail in terms of document control and site start up aspects.
Essential Skills & Qualification
Life science or similar biomedical degree
Significant expertise as a clinical project manager within pharmaceutical R&D in Europe
Experience of managing scope definition, study start up and multiple vendors/contract^aspects
Available to work full time and office based for 6 month of longer
Available within 4 weeks of interview
Software Competence: MS Office, MS Project
Valid Driving License: Essential
Working Language(s): English
Requirement for Business Travel: Yes some
Flexible Working Hours: Yes, core hours on site
Employer: Pharmaceutical Company
Employment Type: Agency Contract
Hours: Full time
Contract Term: 6 Months may extend
Location: UK; M3/M4 access
Plan Start Date: September 2012, please do not apply if you are unable to meet this start date.
Contract Benefits: Day Rate inclusive of benefits
MS Office, MS Project, 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
Assigned Consultant: Ann Maloney at CSL Recruitment on 01932 234 689
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.