Manager, Clinical Laboratory Data Operations- FR

Manager, Clinical Laboratory Data Operations - FR

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Chez Altasciences, nous travaillons tous à l'unisson pour contribuer à la découverte, au développement et à la fabrication de nouvelles thérapies médicamenteuses afin qu'elles parviennent plus rapidement aux personnes qui en ont besoin. Quel que soit votre rôle, nous jouons tous un rôle important et vous aurez un impact significatif sur la santé et le bien‑être des personnes dans le monde entier.

En respectant nos valeurs de développement du personnel, d'orientation client, de qualité et d'excellence, de respect et d'intégrité, nous cherchons à favoriser un environnement de travail passionné et collaboratif et nous sommes à la recherche de personnes talentueuses et enthousiastes, comme vous, pour rejoindre notre équipe en pleine croissance ! Que vous soyez un récent diplômé de l'université ou à la recherche de votre prochaine opportunité de carrière, il est temps de découvrir votre avenir chez Altasciences.
Nous sommes meilleurs ensemble et c'est ensemble que nous sommes Altasciences.

The Manager, Clinical Laboratory Data Operations (MCLDO) serves as the central liaison between the clinical laboratory, study teams, and external clients to ensure accurate data handling and efficient communication. This role oversees all aspects of clinical data management, including review and approval of Data Transfer Agreements (DTA) and Data Transfer Specifications (DTS), configuration of study panels within Clin Spark EDC, and participation in study‑related meetings and client calls.

The MCLDO conducts data analyses to identify trends or shifts in assay performance, ensuring data integrity and quality. Additionally, the position manages operations of the Peripheral Blood Mononuclear Cell (PBMC) Laboratory and supports management in developing ELISA assays tailored to specific study protocols.

• Data transfer agreement (DTA) and data transfer specification (DTS) review and approval, if applicable for paper studies or external clients.
• Build panels on Clin Spark EDC in accordance with protocols.
• Interfacing with the study and project management teams.
• Data analysis to determine possible shifts and trends within assay‑specific results.
• Manage the Peripheral Blood Mononuclear Cells (PBMC) Lab and its associated operations.
• Assist management with building out and running enzyme‑linked immunosorbent assays (ELISA) for protocol‑specific assays.
• Be available for all internal and external client calls as it pertains to data management and all processes within.
• Assist in the Clinical Diagnostic Laboratory.
• Possibly provide direct supervision to a small team, including but not limited to: task delegation, employee development, performance feedback, and support for workplace relations, depending on project scope and organizational needs.

• Bachelor’s degree in an associated science field;
  Chemistry, Biology or other Physical science, preferred.
• Minimum 2 years of related laboratory experience (or, as required by location).
• 2 years supervisory experience in a clinical laboratory setting preferred (or, as required by location).
• MLT/MLS (ASCP) certification preferred.
• MS Word, Excel, Outlook, PowerPoint, Clin Spark, CGM Lab Daq, Math for dilutions and ELISA workup.
• Ability to read and interpret technical documents and industry‑specific manuals. Ability to write advanced reports and correspondence.
• Ability to speak effectively before groups of customers or employees of the organization.
• Understanding of various basic lab assay nomenclature.
• Excellent verbal and written communication skills.
• Well‑developed interpersonal skills are required.
• Personal/professional integrity and proven discretion in handling confidential information.
• Ability to develop strong trusting relationships to gain support and achieve results.
• Capable of managing multiple conflicting priorities.
• Must be self‑directed, motivated, and have a willingness to take the initiative to identify and anticipate client…