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.
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.
Guide, analyze and report in vitro and in vivo biotransformation studies, with focus on analytical method development, metabolite profiling, and reporting. Manage and collaborate with senior staff regarding study execution as it relates to timelines, data quality, and interpretation of results. Interact with clients regarding metabolism data and concepts.
Functional area technical expert in metID concepts, including study design, conduct and interpretation.
Perform or oversee the performance of tasks associated with in vitro and in vivo metID studies.
Design, interpret, implement, document, report, and oversee metID study packages in collaboration with junior-level staff, including analytical methods for analysis of metabolites, metabolic profiling, and MS and MS/MS data collection, using appropriate level of regulatory compliance.
Provide direction for individuals or discrete group, as required.
Independently interpret MS/MS data and assign metabolite structures.
Troubleshoot and/or consult on more complex analytical methods and metabolite profiling.
Keep abreast of literature; interact with peers in the metID scientific arena.
Contribute to continuous improvement initiatives to increase quality or services and operational efficiency.
Independently analyze and prepare data, write reports, and manage study flow.
Ensure quality and timely delivery of the project deliverables to clients.
Independently interact with clients regarding scientific principles and performance of metabolism studies when directed.
Propose and evaluate new technologies, techniques, study designs or equipment.
Provide training and guidance to lower level and new staff as required.
REQUIRED KNOWLEDGE, SKILLS AND ABILITIES
In-depth knowledge of drug metabolism processes, including analytical method development, metabolite profiling, , and structural determination.
In-depth knowledge of laboratory equipment and instrumentation, with particular focus on MS instrumentation (MS and MS/MS data collection and basic interpretation; instrument trouble shooting).
Responsible for overseeing performance of group personnel; Ability to mentor staff in data interpretation/scientific innovation/scientific productivity.
Ability to establish and maintain effective working relationships with coworkers, management, and clients.
Recognized as an effective team member; modeling work on best practices; mentoring team members.
Knowledge and ability to establish and implement good laboratory practices or other documentation.
Good documentation skills; ability to manage and maintain complete and accurate records of experiments.
Attention to detail and accuracy in work against milestones or goals.
Ability to manage/oversee multiple tasks and projects.
Excellent written and oral communication skills.
Knowledge and implementation of safe laboratory practices.
Ability to critically evaluate data and lab processes; propose and implement new approaches.
Ability to oversee and mentor lower level and new staff.
MINIMUM REQUIRED EDUCATION AND EXPERIENCE
PhD in chemistry, biochemistry, or biology or related field and 3 years’ relevant experience; or Master’s Degree in chemistry, biochemistry, or biology or related field and 6 years’ relevant experience or Bachelor’s Degree and 10 years’ relevant experience; or equivalent combination of education, training and experience.
Work is performed in a laboratory environment, full manual dexterity and visual acuity required
May be exposed to potential physical harm from hazardous chemicals, infectious diseases, blood-borne pathogens, toxic materials, toxic gases, electrical hazards, dangerous tools and equipment
Use of keyboard requiring repetitive motion of fingers
Regular sitting or standing for extended periods of time
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™.