As an Associate Principal of the DTAS (Data, technology and Advisory Services) Health Economics / Health Technology Assessment (HE/HTA) practice, you will work directly with life sciences clients as a…
UK jobs. Bigger possibilities.
136,000+ live jobsAssociate Manager - Biochem
On-site in West Lothian·Full-time·Added 7 days ago (last checked 8 Oct)
Overview
Job details
Full-time
Per the ad.
Requirements
Work on-site in West Lothian
No relocation package mentioned.
Have 4+ years of experience
Mid-level role.
Skills
Nice to have
Requirements
What we're looking for
- Bachelor's degree in a Human Biology based science.
- 4 years of relevant experience in a clinical laboratory or clinical trials environment. (Biochem 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
The role
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.
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
Requirements:
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.
Hiring process
1 interview
- Other interviews are conducted on Microsoft Teams, unless otherwise specified.
- Most interviews are conducted in English unless otherwise specified. However, some questions may be asked in local language.
- The use of AI support during an interview or online assessment is strictly prohibited and grounds for disqualification.
About IQVIA
- Industry
- Clinical Research and Health Data
- Founded
- 1982
- Employees
- 50,000–100,000
- Headquarters
- Durham, USA
- Website
- iqvia.com
More jobs like this
or browse Mid-level·Biotech & Life Sciences·Clinical Research and Health Data


