Senior Clinical Data Management Lead

hace 3 semanas


Colombia Syneos Health, Inc. A tiempo completo
Clinical Project Leader for Clinical Data Management

Syneos Health is a leading biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities.

Our Vision

We are continuously looking for ways to simplify and streamline our work to not only make Syneos Health easier to work with, but to make us easier to work for.

Our Approach

We collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to accelerate the delivery of therapies, because we are passionate to change lives.

Key Responsibilities
  • Strong project management skills and knowledge of project management methodologies.
  • Demonstrated staff leadership skills.
  • Experience in Clinical Data Management practices and relational database management software systems.
  • Clinical data management experience or an equivalent combination of education and experience.
  • BA/BS in the biological sciences or related disciplines in the natural science/health care field or Registered Nurse. In lieu of degree, equivalent relevant work experience.
  • Contract Research Organization (CRO) experience preferred.
  • Direct exposure to Oracle Clinical, Rave, or Inform systems.
  • Knowledge of medical terminology, clinical data, and ICH/Good Clinical Practices.
  • Proficiency in MS Windows navigation, Word, Excel, PowerPoint, and email applications.
  • Effective oral and written communication skills.
  • Strong presentation skills.
  • Good organizational, planning, and time management skills with the ability to multitask under tight deadlines while providing attention to detail.
  • Ability to be flexible and adapt to change, to work independently, as well as part of a multi-disciplinary team.
  • Ability to make effective decisions and manage multiple priorities in a highly dynamic environment.
  • Knowledge of ICH/GCP regulatory requirements for clinical studies, in particular requirements applicable to Clinical Data Management.


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