Project Manager Global Site Services Study Start-up
6 month contract- Home based
Our client is one of the world's largest, and well respected drug development services companies with more than 11,000 employees in 60 countries. Our client has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today. With continued growth and investment this Global CRO is looking to appoint a Manager to join their Global Site Services (GSS)/Study Start Up UK team. You will have a flair for team management combined with expertise in optimising study start up activities, thereby allowing client managed studies to get off the ground in a timely manner.
If you're looking for a diverse^and stimulating work environment, one where your unique talents and skills can have a tremendous impact, you'll find it here, our clients collaborative and challenging environment can change the course of your career, seeking to promote a balance between your personal life and professional life you will be in an environment that will allow you to learn, grow and achieve.
Summary of Responsibilities
Ensure effective cross-functional teamwork among project team members including both internal and external ancillary services.
Lead implementation of Six Sigma initiatives on projects as applicable.
Monitor project schedule and scope to ensure both remain on track. Initiate and implement appropriate actions.
Accountable for budget across assigned project(s) including the control and minimizing of write-offs. Proactively identify out of scope activities and ensure necessary change orders are executed.
Proactively engage in both quality assurance and risk management activities^to ensure project deliverables are met according to both our client and client requirements.
Present at external and/or internal meetings.
Ensure client satisfaction.
Supporting new staff in region and integrate them into the study process efficiently
University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology).
Masters or other^advanced degree preferred
Relevant clinical research experience in a pharmaceutical company/CRO, including full project management responsibility.
Experience in managing global (inter-continental) projects in a multi-office^environment.
Financial awareness and ability to actively manage financial tracking systems.
Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system. Demonstrated ability to lead by example and to encourage team members to seek solutions.
Ability to network, negotiate and liaise face to face and remotely with high level internal and external stakeholders in a professional manner
Ability to manage multiple competing priorities and projects without supervision, including strong communication, planning & organizational skills
Thorough working knowledge of study start-up process
Demonstrated Account Management and business development experience with a previous track record working as a Clinical^Project Manager or in a Senior Clinical Study Start-up role would be advantageous
Strong computer skills with an ability to understand access and leverage technology alternatives
A working knowledge of ICH GCP, US FDA regulations, regulations applicable to local office, guidelines, and practices regarding Good Clinical Practices.
Our Clients Offer
Our client's on-going success offers team members unsurpassed growth and career development opportunities.
Our client helps make the miracles of medicine a reality.
Software Competence: MS Office, MS Project
Valid Driving License: Essential
Working Language(s): English
Requirement for Business Travel: Yes
Flexible Working Hours: No
Employment Type: 6 month contract
Hours: Full time
Location: UK; Home based
Plan Start Date: ASAP
Benefits:Pension, Healthcare, Car Allowance, Performance related bonus
MS Office, Medical Affairs,^KOL, publications, IIS, Study Start Up, lifecycle, Clinical Research, Clinical Operations, Clinical R&D, CRA, CTM, Project Management, GCP, Site Manager, observational, 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: Matthew Pike at CSL Recruitment on 01932 219321
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^