I'm looking for...
close

Did you know that your Internet Explorer is out of date?

To get the best possible experience using our website we recommend that you upgrade to a newer version or download another web browser.
A list of the most popular web browsers can be found below. Just click on the icons to get to the download page.

crome
Google Chrome
IE
Internet Explorer
firefox
Mozilla Firefox
opera
Opera

Your browser will need to close to complete the installation and you will need to manually reload the site when finished
Contact Info
QA Officer
Dublin
Buyer
Cork
QA Manager
Meath
R&D Engineer
Galway
QA Manager
Dublin West
QA Manager
Dublin North
Snr QA Specialist
Dublin South
Head of Quality
Dublin West
Biostatistician
Dublin City Centre
QA Manager Biologics
Dublin West
R&D Engineer
Dublin
API Purchaser
Dublin
Program Manager
Westmeath
Apply for this job

Name:

Surname:

Email:

Phone:

Cv:

Salary Expectations:

Education:

Experience:

Current Location:

Notice Period:

Write here your cover note:


If you would like us to create a jobseeker account for you, giving you access to
account management, job alerts and one-click applications, then please tick this box

If you are having difficulty you can always email your cv to applications@lifescience.ie
Details

Clinical Project Manager Group Lead


Reference:ARNW-161818 Location: Dublin
Qualification:DegreeExperience:10+ Years
Job Type:PermanentSalary: Not Disclosed

Clinical Project Manager Group Lead
Our client, a multinational pharmaceutical role are currently recruiting for a Clinical Project Manager Group Lead to join their team on a permanent basis. This is a newly created role due to the growth of the business.

Responsibilities
• Lead and develop the Clinical Project Management team in Ireland to ensure staffing, training and development
• Create & develop local processes to implement the End to End Clinical Trial Service strategy – collaboration with counter-parts globally is essential
• Provide sound leadership and superior decision-making support as well as services’ experience and process excellence to drive quality service implementation, cost optimization and continuous improvement
• Build on existing processes or develop new processes to provide guidance to the clinical trial teams to ensure that industry best-practice standards in operational and performance excellence are met and customer expectations are met or exceeded.
• Drive improvement in performance of service quality, turnaround time, customer feedback and other key performance measures and benchmark against best-in-class
• Establish robust relationships with other Operations teams, understanding the needs of stakeholders to identify potential service opportunities or improvements in service processes
• Provide clinical operational input to activities related to planning, execution and reporting of clinical trials to support clinical trial management
• Proactively identify areas of potential concern, initiating corrective action when necessary, and identify innovative ways to improve productivity. Function as escalation contact point for trial teams
• Ongoing review of clinical trial data in collaboration with appropriate members and Brand Safety Leader, as needed
• Champion cross-functional interaction and collaboration to ensure quality delivery of studies
• In collaboration with QA, manage audits and regulatory inspections and create an audit readiness working environment
• Interact with sourcing department to ensure selection of optimal vendors essential to service delivery and continual optimization of vendor services

Requirements
• Degree or PhD in Life sciences/Pharmacy, with strong knowledge of clinical development and trial execution
• 10 years of clinical research experience, including clinical trial management experience, with solid knowledge of global drug development process
• 4 years of people management experience required, this may include people management in a matrix environment (Responsibility for 5 to 10 direct reports, depending on new trials & programs. Responsible for oversight of provision of Clinical Trials services)
• Excellent understanding of clinical trial methodology, GCP and medical terminology
• Advanced planning and tracking skills with attention to detail. Well-organized, excellent time management with respect to priorities and self-management
• Strong management, interpersonal, communication, and problem-solving skills
• Quick action taker. Involves the right team members in the right situation at the right time
• Ability to mentor, coach associates, and to coordinate interactions with internal and external partners
• Superior people management skills with demonstrated positive leadership, innovative, and

If you would like further Information you can contact the recruiter directly:

Sinead Cullen | Tel: +353 (0) 1 507 9252