What are the responsibilities and job description for the Associate Scientist, In Vitro Metabolism position at IQVIA?
JOB OVERVIEW
Responsible for performing routine analysis and laboratory testing procedures to obtain data from pre-clinical and/or clinical specimens. Provides routine documentation and review of work performed in a timely manner.
RESPONSIBILITIES
- Responsible for performing and documenting analytical procedures in accordance with methods and regulatory guidelines.
- Exercise good judgment in assessing whether analytical procedure is proceeding according to expectations and that the results are within acceptable tolerances through routine data analysis.
- Identify abnormal progress of analytical procedure, potential quality failures, or otherwise unusual results and escalate to senior lab personnel immediately.
- Prepare data analysis results for upload to LIMS system under the guidance of senior level staff.
- Preparation of buffers and solutions for analysis, as required.
- May assist in writing of laboratory procedures and techniques.
- May train junior level staff and assist with onboarding.
- Perform and document calibration and maintenance of laboratory equipment as assigned.
- Perform and document hands on training for other lab personnel in areas of proven competency as assigned.
- Assist in the review and development of laboratory procedures and techniques.
- Assist in the implementation of procedural changes as assigned.
- Notify inventory staff of supply shortages.
- May represent lab team on cross functional projects.
- Participate in continuing education through self-study, attending training sessions and lectures and meetings.
- Production of quality data and documentation in adherence to client deadlines in accordance with regulatory requirements.
- Support safety and 6S requirements and initiatives.
MINIMUM EDUCATION REQUIRED AND EXPERIENCE
- Bachelor's Degree Required Or
- Other Bachelor's degree or equivalent combination of education, training, and experience.
- Bachelor’s degree in relevant scientific discipline plus 6 months experience or Associate’s plus 2 years equivalent; or equivalent combination of education, training, and experience.
REQUIRED KNOWLEDGE, SKILLS, AND ABILITIES
- Requires basic knowledge of assigned technical area, systems and procedures obtained through prior work experience.
- Demonstrates understanding of functional area and responsibilities.
- Working knowledge of regulatory agency standards within the area of responsibility.
- Proficiency with pipetting.
- Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.
- Experience working with automation or specialized laboratory equipment.
- Proficiency with more complex laboratory calculations regarding batches and specimens including averages, means, standard deviations, and various quality control metrics.
- Good computer skills using Microsoft Outlook, Word, and Excel.
- Capable of handling multiple tasks simultaneously.
- Strong attention to detail and accuracy.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Q² Solutions is a leading clinical trial laboratory services organization with end-to-end laboratory services and secure, enterprise-wide biospecimen and consent management solutions. https://www.q2labsolutions.com/careers
We are committed to providing equal employment opportunities for all, including veterans and candidates with disabilities. https://jobs.iqvia.com/q2-solutions-eoe
As the COVID-19 virus continues to evolve, Q² Solutions' ability to operate and provide certain services to customers and partners necessitates Q² Solutions and its employees meet specific requirements regarding vaccination status. https://jobs.iqvia.com/q2-solutions-covid-19-vaccine-status
