Project Manager - Medical Imaging
- Employer
- Parexel
- Location
- Nottingham, United Kingdom
- Salary
- Competitive
- Start date
- 15 Mar 2019
- Closing date
- 24 Mar 2019
View more
- Discipline
- Clinical Research
- Hours
- Full Time
- Contract Type
- Permanent
- Experience Level
- Experienced (non-manager)
Job Details
This role is based in our new modern state of the art office in Nottingham city centre which has excellent transport links and has a great working environment and the feel of an innovative technology company.
The primary role of the Project Manager is to provide tactical management, administration, and leadership to project teams in order to ensure that the project proceeds on time and within budget. The position provides the client with timely project status information and serves as the key operational interface between the client and Medical Imaging.
Key Accountabilities
- Responsible for the delivery of PAREXEL Informatics products and services to sponsors within expected timelines and budget
- Lead, manage and motivate the multidisciplinary team
- Resource planning and management
- Utilize project management tools to plan, track, prioritize and communicate timelines and deliverables to the project team and sponsor
- Assess project quality and risk
- Proactively investigate and resolve issues
- Manage the study to contract, including proactive management of budget, pass-through costs and contract amendments where necessary
- Actively manage the timelines considering impact on resources and revenue forecasting
- Prepares project timeline associated with the validation process
- Facilitates validation of applications
- Prepares requirements specifications documentation on project specific database application
- Conducts study start up meetings (internal and external)
- Conducts ongoing study team meetings
- Provides timely notification of all appropriate parties with deviations from timelines and/or deliverables
- Conducts regular communication with team members, formal and informal, regarding study status or any other changes
- Utilizes delegation skills to obtain maximum productivity and team involvement
- Performs/ facilitates project specific team training
- Receives all necessary client signatures on the critical path
- Facilitates preparation of study analysis plan/ Charter
- Manages Independent Review process
- Facilitates preparation of all study specific manuals
- Maintains necessary 21 CFR Part 11 guidance documentation
- Able to address 21 CFR Part 11 guidance with respect to project
- Maintains signed copies of all financial and study specific documentation per the SOP
- Able to identify work done as it relates to study exhibit/contract (within or out of scope)
- May assist with therapeutic departmental strategies and goals
- Ensure compliance with SOPs and other relevant FDA regulations.
- Work collaboratively with eClinical program managers and Integration Managers to ensure delivery of the complete and seamless service to sponsors
- In projects with PAREXEL-CRS, proactively support the creation of a multi service and single company perception for our Sponsors
Qualifications
Skills
- Excellent interpersonal, verbal and written communication skills
- Client focused approach to work
- A flexible attitude with respect to work assignments and new learning
- Ability to manage multiple and varied tasks with enthusiasm and prioritize workload with attention to detail
- Willingness to work in a matrix environment and to value the importance of teamwork.
- B.A. or B.S. in scientific field (or equivalent) and/or relevant experience required
- Fluent in English
- Minimum 1-4 years relevant work experience. Experience in an imaging, clinical, or technical operations environment required. Knowledge of project management concepts and approaches preferred
- Proficient in Microsoft Office products including, Word, Excel, PowerPoint, Project
- Licenses, if any: (i.e. Board Certification, Medical License, imaging certificates, etc.)
- Ability to do some travel
Apply today to begin your journey!
Company
When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.
How to describe Parexel’s culture in one word:
Working With Heart™ - Christina's perspective:
Careers Blog | Our Culture | Diversity, Equity & Inclusion | Benefits | Our Hiring Process
Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere.
- Website
- http://www.parexel.com/
- Telephone
- +44 1895 238000
- Location
-
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
United Kingdom
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