About this opportunity
Associate Manager
IQVIA Laboratories – Central Laboratory Service
We are a comprehensive global central laboratory services supporting clinical trials in countries around the world. Meeting the demands of today’s drug, device and diagnostics development environment requires a next generation service provider.
IQVIA Laboratories helps sponsors enable laboratory testing in global clinical trials by providing specimen collection kits, a courier network, a biorepository, plus project management and data management. With extensive scientific expertise and industry leading capabilities in lab services, biomarkers , companion diagnostics , esoteric testing, high quality data and analytics , as well as global logistics and biorepository & specimen management , IQVIA Laboratories helps biotech and pharmaceutical companies meet their development needs.
Join us on our exciting journey!
Job Overview:
Responsible for supervising a team of lab staff and ensuring effective operational delivery and for setting day to day operational activities for the team with a focus on daily delivery.
Under the mentorship of management, responsible for hiring, training, and performance management of staff.
Supervises the daily activities of assigned laboratory work group(s) through appropriate delegation, technical skills training, and work supervision. Meets regularly with staff and senior management to discuss and resolve workload and technical issues.
Responsible for ensuring activity in the team meets safety guidelines. Drives individual accountability for safety across the team. Identifies opportunities for improvements in safety.
Responsible for the review of laboratory metrics to identify initiatives as well as establish additional metrics such as cost savings that are associated with process improvement initiatives.
Ensures policies, practices and procedures are understood and followed by direct reports, customers and stakeholders.
Ensures timely and appropriate resolution of CAPA and quality incidents, quality and compliance metrics, root cause analysis and improvement.
Assists in establishment and revision of laboratory policies and procedures. Maintains appropriate control and quality assurance procedures. Ensures compliance with safety requirements.
Requirements:
Bachelor’s degree in a Human Biology based science.
4 years of relevant experience in a clinical laboratory or clinical trials environment. (Immunology based)
Experience in technical leadership and cross-functional collaboration
Proficiency with LIMS and other laboratory data systems.
Familiarity with CAPA processes and quality systems
Ability to analyse and interpret complex data.
Ability to effectively coordinate and execute multiple tasks or projects simultaneously.
Ability to effectively write scientific and technical documents
Understanding of LEAN 6 Sigma principles
Join IQVIA to see where your skills can take you
Global exposure
Variety of therapeutic areas
Collaborative and supportive team environment
Access to cutting-edge and innovative, in-house technology
Excellent career development and progression opportunities
Work-Life Balance, with a strong focus on a positive well-being.
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 committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Job details
How this role compares
Computed from every other active Drug Discovery & Preclinical Research role in our database, not just this employer's listings.
We currently track 111 comparable Manager Drug Discovery & Preclinical Research roles across 39 biopharma companies.
Salary context
47 of 111 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 111 comparable roles
+ 9 more countries
Seniority mix
111 of 111 peers have a known seniority level
Therapeutic area mix
12 of 111 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
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How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.