LCMS Bioanalytical Project Manager / Study Director (Future Opportunities) (1724501) - (R1016304) in Ithaca, NY at IQVIA™

Date Posted: 11/10/2018

Job Snapshot

  • Employee Type:
    Full-Time
  • Location:
    Ithaca, NY
  • Experience:
    At least 5 year(s)
  • Date Posted:
    11/10/2018
  • Job ID:
    R1016304

Job Description

Launched in 2015, Q2 Solutions is a leading global clinical trials laboratory services organization. We help biopharmaceutical, medical device and diagnostics customers improve human health through innovation that transforms science and data into actionable medical insights. Q2 Solutions is a quality driven, responsive partner with strong global experience and deep scientific and medical expertise. The Q2 Solutions joint venture was formed by Quintiles and Quest Diagnostics, combining the best of each parent organizations clinical trials laboratory services capabilities.

Description

 
We are always looking for new talent to join Q2 Solutions. To be considered for a future Project Manager / Study Director position, submit your resume. If your qualifications, experience and skill sets align with the position requirements, one of our recruiters will connect with you.  
 
 
 
PURPOSE
 
The BioServices Project Manager is the primary point of contact for our external customers. The focus of the BioServices Project Manager is to provide exceptional customer service while ensuring that all work meets Q2 Solutions scientific standards.
 
 
RESPONSIBILITIES
 
  • Provide oversight and conduct of a project throughout its life at Q2 Solutions, including method development, method validation, and sample analysis.
  • Work closely with Technical Writing and QA to ensure projects are completed on schedule.
  • Review validation and bioanalytical reports for completeness.
  • Maintain all communication with customers providing daily updates on all active projects while being vigilant for opportunities to earn additional business.
  • Work with the customer to resolve sample discrepancies.
  • Monitor the progress of all assigned projects and alert management if work falls behind schedule.
  • Provide regular project status updates to management.
  • Participate in weekly scheduling and revenue update meetings and provide updates on project progress.
  • Submit accurate weekly assessment of resource requirements for scheduling purposes
  • Prepare validation and sample analysis plans.
  • Review data (run binders, data tables, etc) for regulatory compliance and scientific quality.
  • Address issues from QC and QA review for run binders.
  • Conduct thorough investigations of all failed runs.
  • Lead method troubleshooting investigations. Assemble group of pertinent technical resources and write up investigation report.
  • Provide project trackers for client communications and lead regular teleconferences to discuss project progress
  • Coordinate customer visits.
  • Visit customers.
  • Work with business development staff to prepare quotes for assigned customers.
  • Approve validation experimental designs.
  • Prepare data for external presentations.
  • Ensure projects are archived in accordance with Q2 Solutions SOP
 REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
  • Ability to achieve results through collaborative efforts with others.
  • Understanding of liquid chromatography and combination with mass spectrometry.
  • Experienced in sample extraction and routine laboratory procedures.
  • Understanding of method development and validation of assays
  • Ability to interact with external and internal clients, and work to objectives/timelines
  • Excellent attention to detail and communication skills
  • Ability to provide verbally communicated or draft procedures
  • Ability to establish and maintain effective working relationships with coworkers, managers and clients.

Job Requirements

MINIMUM REQUIRED EDUCATION AND EXPERIENCE
Bachelor’s Degree in a scientific field with 5 years’ related experience; or equivalent combination of education, training and experience in GLP laboratory environment.
PHYSICAL REQUIREMENTS
  • Extensive use of keyboard requiring repetitive motion of fingers.
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech .
  • Regular sitting for extended periods of time .
  • Some travel required.
EEO Minorities/Females/Protected Veterans/Disabled
 
 

We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve human health outcomes.

Whatever your career goals, we are here to ensure you get there!

We invite you to join IQVIA™.


Job ID: R1016304