Summary: Drive biospecimen strategy, ensure flawless sample collection and analysis, and guarantee data integrity in global clinical trials to accelerate life-changing therapies. Highlights: 1. Be the biospecimen champion in global clinical trials 2. Lead biospecimen strategy and oversee the entire sample lifecycle 3. Ensure data integrity and accelerate life-changing therapies Madrid, Spain \| Full time \| Home\-based \| R1536829**Job available in additional locations** **Your Mission** Be the **biospecimen champion** in global clinical trials! Drive strategy, ensure flawless sample collection and analysis, and guarantee data integrity. Your expertise powers breakthrough science and accelerates life\-changing therapies.**What You’ll Do*** **Lead Biospecimen Strategy:** Collaborate with clinical development teams to define and execute sample plans. * **Own the Lifecycle:** Oversee collection, analysis, and data transfer for all biospecimens. * **Technical Leadership:** Set up and manage labs for kit building, sample handling, and testing. * **Protocol Expertise:** Provide input on sample\-related sections in protocols and consents. * **Risk Management:** Identify and escalate biospecimen\-related risks; implement solutions. * **Training \& Support:** Develop lab manuals and training materials for clinical sites. * **Data Excellence:** Ensure accurate data transfer and reconciliation with trial data managers. * **Close\-Out Mastery:** Manage sample disposition—storage, return, or disposal—at study end. * **Budget Oversight:** Review lab proposals, forecast costs, and validate invoices. **What You Bring*** **Education:** Bachelor’s degree in Life Sciences or related field. * **Experience:** Strong background in clinical trials and biospecimen management. * **Skills That Shine:** + Deep knowledge of sample logistics and ethical considerations. + Ability to collaborate across functions and geographies. + Strong organizational and problem\-solving skills. + Technical expertise in lab operations and data integrity. + Proficiency in SOP compliance and risk mitigation. **Core Strengths** ✅ Collaboration ✅ Innovation ✅ Ownership ✅ Quality Focus ✅ Communication**Please note this role is not eligible for the UK visa sponsorship.***Please note: due to sponsor requirements for the role only candidates based in the listed location/s will be considered. Any applications from candidates based outside of these locations will not be considered.* 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. The potential base pay range for this role, when annualized, is 217\.800,00 zł \- 404\.600,00 zł. 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.
David Muñoz
Indeed · HR
David Muñoz
Indeed · HR
