Senior Scientist- Assay Development - (R1047263) in Research Triangle Park, NC at IQVIA™

Date Posted: 11/10/2018

Job Snapshot

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

SUMMARY:
The Senior Scientist will be responsible for development and validation of molecular assays requiring isolation of nucleic acid and detection using various PCR methods, nucleic acid sequencing, genotyping, or gene expression analysis. The ideal candidate will have a molecular biology, oncology, immunology, and/or human genetics background, strong communication and organizational skills, leads by influence, and strong problem-solving skills.

RESPONSIBILITIES:
  • Development and validation of molecular assays using genomic technologies such as DNA sequencing, amplification, genotyping, and gene expression.
  • Proficient in nucleic acid (DNA, RNA) extraction methodologies involving liquid and tissue specimens/samples.
  • Evaluates new genomic technologies and drives their implementation within the assay development team.
  • Provides Subject Matter Expertise (SME) in molecular biology, oncology, immunology, and/or human genetics. 
  • Serve as a technical or scientific lead on internal and/or client projects.
  • Contributes to ideas and perspectives in client discussions. Engage and communicates with clients.
  • Independently designs and executes experiments to develop assays.
  • Responsible for sample and specimen handling of biological samples, including bacteria/viruses requiring BSL-2 containment.
  • Demonstrated ability to summarize, analyze and convey complex information clearly and adjust communication to the audience.
  • Contributes to or may author publications (posters, patents, journals), as applicable.
  • Responsible for, with increasing accountability for, creation and review of experimental designs, protocols, plans, procedures, product/process documents and reports to achieve department objectives.
  • May oversee/direct (be accountable for) lab work or work carried out by other associates in assay development.
  • Leads by example in following all policies, procedures as required and proactively identifies and remedies problems.
  • Independently executes defined protocols and procedures and creates technical reports on feasibility and validation projects.
  • Liaisons with other functions such as Project Services, Bioinformatics, Software, Operations, and Quality.

Job Requirements

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES:
  • Technical expert on use of molecular biology techniques including hands-on experience with high throughput DNA Sequencers, genotyping, and Real-Time PCR equipment.
  • Strong oral and written communication skills; demonstrated ability to present and write technical Information and train staff on molecular methods.
  • Has in-depth understanding of risk management concepts and can assess product, process, project and schedule risks.
  • Able to remove simple or moderately complex road blocks.
  • Knowledge of Companion Diagnostics and/or Design Controls is preferred but not required.
  • Excellent computer skills including proficiency with Microsoft Office applications, as well as experience in bio-statistical software.
  • Demonstrated understanding of molecular biology, analyze data, and solve technical problems.
  • Demonstrates Q2 Solutions values of Quality, Teamwork, Leadership, Accountability, and Integrity.
  • Clinical laboratory assay development or CLIA experience preferred but not required.
  • Ability to effectively navigate on-line biological databases including NCBI (e.g. PubMed, Entrez, etc.), EMBL, Sanger, etc.
  • Accountable for decisions within scope of work.  Uses sound judgment and thinks through impacts of situations, options, and broader impact as well.
  • Ability to influence tactical decisions within assay development and across functions within product line.
  • Motivates and engages team mates by asking for input and listening to other ideas.
  • PhD preferred but not required.
PREFERRED QUALITIES
  • Strong molecular biology background.
  • Strong organizational skills.
  • Effective communication skills.
  • Ability to effectively execute multiple tasks.
  • Able to drive problem solving activities within area of work. Uses Pareto charts, 5 Whys, fish bone diagrams to get to root cause.
  • Strong analytical skills.
  • Leads using influence.
  • Strong interpersonal skills.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE:
  • BS/MS Degree or educational equivalent in cell biology, molecular biology, oncology, immunology, human genetics, or related field with a minimum of 8 years relevant experience; or equivalent combination of education, training and experience.

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: R1047263