Clinical Data Manager I-BioM
hace 2 días

Job Overview :

COVANCE is a leading global drug development services company and we provide support to the Pharmaceutical and Biotechnology industries.

We are recruiting for our team in Latin America and are currently seeking to hire a Clinical Data Manager I. This is a permanent, full time position.

Covance’s ongoing success offers team members unsurpassed growth and career development opportunities.

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

This is your chance to become part of a team that helps to bring miracle of medicine to market sooner.

There is no better time to join us!

Education / Qualifications :

  • University / college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.
  • g., nursing certification, medical or laboratory technology).

  • Knowledge of drug development process.
  • Knowledge of effective clinical data management practices.
  • Fluent in English, both written and verbal.
  • In lieu of above requirement, approximately four years’ experience in related field (e.g. pharmaceutical, laboratory, data analysis).
  • Preferred :

  • Knowledge of Covance and the overall structure of the organization.
  • Knowledge of Covance standard operating procedures.
  • Experience :

  • Four years of combined early or late stage Data Management experience with one year of direct sponsor management and one year technical mentoring experience.
  • Proven experience of handling customer negotiations and exposure to managing Scope of Work and budgets.
  • Knowledge of clinical trial process, DM, clinical operations, biometrics, and system applications to support operations.
  • Proven ability to lead by example on project strategies and achievement of department goals, objectives and initiatives and to encourage team members to seek solutions.
  • Working knowledge of the relationship and regulatory obligation of the CRO industry with pharmaceutical / biotechnological companies.
  • Time management skill and ability to adhere to project productivity metrics and timelines.
  • Ability to work in a team environment and collaborate with peers.
  • Good organizational ability, communication and interpersonal skills.
  • Team working skills and good collaborator skills.
  • Constructive problem solving attitude while deadline focused with time demands, incomplete information or unexpected events.
  • Knowledge of medical terminology.
  • Knowledge of science or a scientific background is preferred.
  • Good oral and written communication skills.
  • Preferred :

  • Through knowledge of Covance, the overall structure of the organization and Standard Operating Procedures (SOPs).
  • Two or more years of Electronic Data Capture experience.
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