Clinical Laboratory Study Manager

This is a fully remote position, open to applicants in Argentina.

📋 Description

• Collaborate closely with the leadership of Precision Medicine and interdisciplinary study teams.

• Ensure the proficient management of quality samples and data to facilitate biomarker and non-biomarker assessments.

• Engage in interdisciplinary study team meetings and workstreams.

• Assist project management and study set-up teams in the formulation and validation of specialized laboratory databases.

• Oversee all activities related to the planning and execution of the biosample process.

• Supervise the acquisition and testing of clinical trial samples designated for biomarker research.

• Collaborate with data management and biostatistics leads to establish methods for capturing, blinding, transferring, and reporting biomarker data for clinical trials.

• Offer guidance and training to clinical teams and investigative sites on the collection, storage, and shipment of biospecimens.

⛳️ Requirements

• At least 6 years of clinical research experience in academic settings, Contract Research Organizations, the pharmaceutical industry, or biotechnology.

• Solid understanding of the clinical drug development process and clinical databases, alongside knowledge of ICH, GCP guidelines, and applicable US FDA and/or local country regulations.

• Proficiency in Microsoft Office, particularly with advanced Excel skills.

• Competence in programming languages such as Python, R, Perl, SQL, or others, along with familiarity with APIs and Linux/Unix environments.

• A bachelor’s degree in life sciences or a related field (e.g., science, technology, engineering, or mathematics) or equivalent relevant work experience.

🏝️ Benefits

• Health insurance

• Retirement plans

• Paid time off

• Flexible work arrangements

• Professional development