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Job Details

Associate Project Manager

Company: Premier Research
Location: Europe wide
Reference: 754JK
Closing Date: 13 Dec 17
Type: Full Time
Salary (£): Competitive
Benefits: Comprehensive

Job Summary:

Premier Research helps highly innovative biopharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research. We’re looking for a talented and energetic Associate Project Manager in the EU to join our team!

Requirements:

Premier Research helps highly innovative biopharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research. 

We’re looking for a talented and energetic Associate Project Manager in the EU to join our team!  This position can be offered from any EU location where we have an office presence.

Description

Premier Research helps highly innovative biotech and specialty pharma companies transform life-changing ideas into reality. We have positioned ourselves right in the middle of the action, targeting unmet needs in analgesia, neuroscience, oncology, pediatrics, and rare diseases.

Working at Premier Research means being an individual - you will be recognised for what you do and you will truly have an impact. You will be working in a friendly environment with colleagues who are genuinely supportive regardless of location or seniority.

Premier Research is on an exciting journey - there is a true buzz throughout the company, so come and be part of it! 

We’re looking for an Associate Project Manager to join our team! This is a permanent role to be located in one of our European offices. 

Imagine. Inspire. Innovate. Impact. With Us.

You’ll be accountable for:

  • Shared responsibility with the Project Manager or Project Director for overall delivery of full service projects
  • May be solely responsible for projects which are limited in size or scope
  • Ensuring successful cross functional management and oversight of the project team, including Regulatory, Clinical Operations, Biometrics, and Medical Affairs/Safety, to support milestone achievement and overall project delivery
  • Ensuring adherence to project budget and scope of work to realize project profitability
  • Ensuring all project tasks are completed in accordance with project plans
  • Ensuring effective communication is maintained and project status reports and monthly progress reports are provided both internally and externally
  • Ensuring adequate resourcing is available to meet project deliverables and milestones
  • Acting as the liaison between Premier Research and the customer for their study or specific portion of the study to which they are assigned. 
  • Chairing project team meetings or teleconferences 
  • Facilitating team training in accordance with protocol and/or project requirements, including therapeutic, protocol specific, and process training
  • Developing project plans for all phases of the project lifecycle, including quality, risk management and proactive contingency plans, ensuring that issue escalation and resolution is clear
  • Overseeing project documentation, ensuring Trial Master Files are completed by the functional groups and audit ready
  • Supporting study audits and responds to audit reports
  • Reviewing and approving project expenses and ensures all study related contractual and budgeting issues are upheld and performed
  • Providing accurate forecasts to ensure timely invoicing
  • Identifying out scope of work changes across all functional areas and assists in securing Change Orders
  • Assisting in Business Development activities including leading proposal presentations in partnership with Business Development and Scientific Account Leadership
  • Identifying, recruiting and managing central vendors

You’ll need this to be considered:

  • Undergraduate degree in a clinical, biological, scientific, or health-related field
  • Previous relevant experience in a pharmaceutical company/medical device company/CRO including trial management support or equivalent or a combination of experience and education
  • Budget/finance experience on a project level
  • Experience in all phases of a clinical study life cycle
  • Good therapeutic and protocol knowledge
  • Knowledge of ICH/GCP regulations
  • Working knowledge of FDA Guidance Documents/EU Directives/ISO14155 regulations, drug/device development, and clinical monitoring procedures
  • Highly confident and effective presenter
  • Fluent verbal and written English
  • Strong verbal and written communication skills
  • Willingness to travel

Apply for this job: Associate Project Manager

Contact Information:

Address:  European Headquarters
1st Floor,
Rubra 2
Mulberry Business Park,
Wokingham,
RG41 2GY
England
View our Profile Page
Tel:  +44 (0) 118 936 4000
Fax:  +44 (0) 118 936 4001
Website:  Visit Our Web Site

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