Offer summary

Qualifications:

Bachelor's degree in a relevant field such as life sciences or clinical research., Strong problem-solving, influencing, and negotiation skills., Experience in a matrix environment with multi-disciplinary teams., Understanding of clinical sample testing methods..

Key responsabilities:

Execute the biospecimen strategy for clinical studies from start to finish.

Provide input on biospecimen logistics and analysis for each study.

Collaborate with partners and internal teams on risk and issue management.

Develop study-specific sample collection and analysis plans.

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Job description

Responsible for the end-to-end execution of the biospecimen strategy for the Global Clinical Operations supported clinical studies.

Key accountabilities

For each clinical study, provide input and solutions for all biospecimen logistics and analysis, considering all ethical and regulatory requirements.
Collaborate with strategic partners to enable implementation of each biospecimen strategy.
Collaborate with internal project team in areas of end-to-end risk, relationship and issue management related to biospecimen collection and analysis.
Collaborate with TDM for eCRF development, data transfer and reconciliation ensuring timely analysis, proper consent, and oversight of all biospecimens

Deliverables

Study specific sample collection and analysis plan.
Lab kits and training materials on the technical aspects of biospecimen collections for the clinical trial sites.
Ensure analysis and data transfers per study requirements

Key skillsets

High problem solving, influencing, and negotiation skills
Leadership skills in a matrix environment, with multi-disciplinary and networked teams
Understanding clinical sample testing methods

This role is not eligible for UK visa sponsorship

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

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