To be eligible for this position, you must reside in the same country where the job is located.

QUALIFICATIONS

• Bachelor’s Degree required or o ther equivalent combination of education and experience.
• 1 year or more of experience in a regulated laboratory environment.
• Sound knowledge of principles, theories, and concepts in job area.
• Working knowledge of any applicable regulatory standards within area of responsibility, such as Good Laboratory Practices (GLP).
• Proficiency with pipetting techniques.
• Knowledge of laboratory safety and infection control procedures and practices including standard precautions and hazardous chemical handling.
• Strong technical knowledge of complex testing procedures and science supporting analysis.
• Proficiency with complex laboratory calculations regarding batches and specimens.
• Ability to troubleshoot laboratory equipment and resolve process issues.
• Good computer skills including proficiency with Microsoft Excel, PowerPoint and Word.
• Effective organizational and interpersonal skills.
• Effective communication and presentation skills.
• 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.
• Applicable certifications and licenses as required by local regulations.
  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide . Learn more at https://jobs.iqvia.com
  IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
  The potential base pay range for this role, when annualized, is $46,200.00 - $96,200.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits

• Executes techniques to ensure biological sample is prepared for subsequent analysis.
• Executes techniques related to assigned area of work, such as extractions from biological matrices, tissue preparation, or purification.
• Responsible for offering subject matter expertise to assist in technical transfer of methods.
• Performs and documents hands on training for junior lab staff in areas of proven competency as assigned.
• Responsible for performing and documenting testing in accordance with SOPs and applicable regulatory guidelines.
• Identifies and documents potential performance errors or otherwise unusual results and escalate to senior lab personnel.
• Assists in process improvements to increase data quality, lower costs, or reduce turnaround times to include, updating standard procedures, assisting with troubleshooting.
• Responsible for clear, accurate, and timely communications with cross functional stakeholders.
• Makes and records observations, perform calculations, and collect and prepare data for evaluation.
• Documents all project work according to Q2 Solutions and regulatory processes and procedures, as applicable.
• Assists in maintaining laboratory equipment and may offer suggestions for new equipment.
• Assists in good housekeeping of the lab environment, consistent with 6S standards.
• Assists in maintaining adequate inventory.
• May be responsible for work requiring specialized techniques and waste management, such as with radioactive materials.
• May assist with assay/method development and validation, attending pre-validation meetings and review of methods to be utilized in validation.
• May lead a laboratory or cross functional project and assist with implementation of changes.
• May interface with applicable LIMS system for workflow management.
• May work with automated instrumentation.
• May perform routine data analysis, as required.
• Supports lab safety, and complies with company’s procedures and regulatory requirements, as applicable.Participate in continuing education through self-study, attending training sessions and meetings.