Clinical Project Manager

Job Location	Newcastle-under-Lyme
Education	Not Mentioned
Salary	55,000 - 60,000 per annum
Industry	Not Mentioned
Functional Area	Not Mentioned
Job Type	Permanent , full-time

Job Description

The successful candidate will play a key part in a product development programme from concept through to production. As Clinical Project Manager you will work closely with all departments, and external contractors.The Clinical Project Manager will be involved in planning and directing team members involved in clinical research projects to ensure projects are delivered in line with clinical goals and objectives. The Clinical Project Manager will be the main contact for vendors and will be responsible for the preparation and review of all documents related to clinical projects.Working closely with the Clinical Research Director, key duties and responsibilities will include:

Provide timely issues resolution, expert knowledge and key decisions at each stage of the project
Ensure project budget is adhered to
Report project progress to key stakeholders
Establish and maintain key relationships - both internal and external
Negotiate with and influence key stakeholders at all levels
Maintain up to date knowledge of advances in key project management techniques
Monitor and report on the progress of clinical trials, including budgets and timelines
Prepare, oversee and review documents related to clinical study
Ensure availability of resources assigned to clinical study
Review and approve invoices presented
Resolve issues and contribute to improvement strategies for the delivery of future studies
Work with the study team to outline priorities and resolve any conflicts that may arise

Key skills and experience required:

Excellent communication skills are essential
Ability to demonstrate good problem solving, organisational and leadership skills are essential
Key attention to detail
Ability to work to set timeframes or deadlines
Ability to motivate the study team
Experience in writing clinical study procedures/clinical documents would be a strong advantage

Candidates must have previous experience in the field of clinical research, including a project lead role.Candidate with a CRO or biomedical background would be of particular interest.This role is based on site and will include work in a laboratory environment.Hours of work: Monday - Friday, 9.00am - 5.00pmHolidays: 25 days + bank holidays

Keyskills :
BiomedicalClinical TrialsCommunication SkillsProject ManagementCRO

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