• Sr Project Manager, Laboratory Jobs in United States Of America - 23758915

  • United States Of America, Usa
  • Save Job
  • 2 - 5 Years
  • Posted : above 1 month

Job Description:


Senior Project Manager, Laboratory

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries The Senior Project Manager will ensure client satisfaction by acting as the Clients main contact in all matters regarding ICON Laboratory Services (ILS), including the setup and day-to-day management of studies, attend and represent ILS at Client meetings, manage studies in accordance with Good Clinical Practice, provide Clients with regular study updates and communicate study progress to Clients and PM Leadership in a responsible and professional manner, represent Project Management at internal interdepartmental meetings or interdivisional meetings within ICON, help train more junior PMs, act in an advisory role to those less experienced on the team, and work to enhance team tools and practices by actively recommending suggestions for improvements in efficiency, serve as the tactical site supervisor for project manager in the absence of a Team Lead for work related and administrative tasks and take on additional responsibilities to enhance the overall PM Team tools and Practices, as defined by Management

Overview of the Role

Recognize, exemplify and adhere to ICONs values which centers around our commitment to People, Clients and Performance
As a member of staff, the employee is expected to embrace and contribute to our culture of process improvement with a focus on streamlining our processes adding value to our business and meeting client needs
Travel (approximately <20 PERCENT ) domestic and/or international
Act as the sponsors main contact person in all matters regarding our central laboratory services, following up and responding to clinical study specific inquiries from Sponsors, Physicians, CRA and CRO representatives and the ICON Site Services Department
Review newly assigned protocols and Amendments Coordinate and manage the completion of the Clinical Laboratory Worksheet (CLW) and communicate information as required to other departments within ICON Laboratories (and ICON Clinical CRO if appropriate)
Enter protocol parameter information into PACS//ICOLIMS and other systems for new and/or amended protocols Prepare and QC clinical study specific materials
Ensure that proper guidelines for communication are set at study start-up and maintained throughout a study by creating and updating the study specific Communication and Escalation Plan Ensure adherence to the protocol specific monitoring plan Maintain clinical study specific study files and ensure that all appropriate documents are properly maintained Ensure that all necessary documents are archived at study closure
Provide Sponsors with study management reports Provide client with support on ICOLabs system Inform team leader about study progress
Proactively monitor study budget
Set the timelines for and monitor the progress of shipment requests for storage samples and verify data
Attend and represent ICON at Sponsor Investigator Meetings, Kick-Off Meeting, Bid Defenses or Initiations
Develop new tools, train new employees
Performs additional relevant responsibilities as requested by management

Role Requirements

Bachelors degree or local equivalent in Science, Business or related Field
Minimum of 2 years of experience working in a clinical laboratory , clinical trials, or customer management/account management role in a life sciences related organization
Minimum of 1 years of Project Management experience in a service area serving clinical trials, such as IVRS, Clinical Supplies Packaging and Distribution, Medical Imaging, Data Management, or Electronic Data Capture
Working familiarity with Word, Excel, PowerPoint
Excellent Oral and Written Communications
Ability to Multi-Task
Ability to remain composed and professional in stressful situations, performing effectively with shifting priorities, workload and external pressures
Excellent Presentation Skills
Organizational Agility
Ability to work with, and maintain the confidentiality of customer proprietary information
Mastery in following established processes and use of all laboratory PM tools (eg configuring laboratory databases, tracking results, ordering supplies, )
Knowledge and familiarity with the clinical trials industry
Ability to successfully perform job functions with little or no supervision
Ability to effectively apply learned principles to broader situations

Benefits of Working in ICON

Other than working with a great team of smart and energetic people, we also offer a very competitive benefits package This varies from country to country so a dedicated recruiter will discuss this with you at interview stage

We care about our people as they are the key to our success We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Healthcare, Biotechnology/Pharmaceutical/Medicine
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 06th Apr 2020

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