Trial Data Manager - Future positions
Merck Sharp & Dohme Corp
Vicente López, AR
hace 6 días


MSD is a global health care leader with a diversified portfolio of prescription medicines, vaccines and animal health products.

Today, we are building a new kind of healthcare company one that is ready to help create a healthier future for all of us.

Our ability to excel depends on the integrity, knowledge, imagination, skill, diversity and teamwork of an individual like you.

To this end, we strive to create an environment of mutual respect, encouragement and teamwork. As part of our global team, you’ll have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career.

This posting is a pipeline position which is used for resume collection. We are currently collecting resumes for further opportunities at MSD Argentina and will contact you as soon as an opportunity arises!

Position Objectives

Candidates will have the skills necessary to thrive in a dynamic and growing company environment, as he / she assists Clinical Research staff in the conduct of clinical trial activities in accordance with Standard Operating Procedures and all applicable regulations governing the conduct of clinical trials.

Responsibilities, but no limited to :

  • Develops and maintains the clinical data management plan, deliverable-based contract, and project schedule at the trial-level;
  • Documents clinical data management-related technologies, processes, vendors, and methods used in the collection, validation, and management of clinical trial data for protocol(s) within a development program;
  • Solicits and defines trial-level requirements for data collection and validation at the trial-level;
  • Manages trial-level data quality and completion of database lock and post-database lock activities.
  • Qualifications

    Qualifications & Experience

    Experience & Skills desirable :

    Education : Bachelor's degree, preferably in life sciences, computer science, or related discipline.

  • Experience in Clinical Data Management;
  • Full life-cycle experience in clinical data management (data collection system development through database lock and close-out);
  • Experience working with project management tools and processes;
  • Experience leading a cross-functional team responsible for multiple protocols;
  • Experience with managing outsourced studies preferred;
  • Particularly important skills include flexibility; logical thinking; ability to prioritize day-to-day and critical tasks;
  • willingness to adapt quickly to changing business conditions and learn new skills; interpersonal and team building skills.

    Our employees are the key to our company’s success. We demonstrate our commitment to our employees by offering a competitive and valuable rewards program.

    Our Company’s benefits are designed to support the wide range of goals, needs and lifestyles of our employees, and many of the people that matter the most in their lives.

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