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Clinical Trial Coordinator

Lancesoft Inc.
Woodcliff Lake, New Jersey, United States
February 06, 2017


Basic understanding of clinical study processes, with specialized technical

skills to deliver own work within the clinical study team. Ability to work

semi-autonomously with strong organizational, prioritization and analytical


Liaises with other functional areas on study-related processes.

Effectively manages time to meet project deliverables and deadlines in a manner that minimizes rework.

Takes appropriate care to ensure quality of data.

Keeps team and supervisor informed and up-to-date on information directly related to own position in the clinical operations study team.

Minimum of college degree in a relevant discipline.

Bachelor's degree in relevant scientific discipline preferred.

Must possess strong Microsoft Excel and other computer skills.

Experience in Oncology preferred.

Minimum of 3 years in Pharmaceutical Company with relevant experience.

General knowledge of basics of clinical operations.

- Familiarity and experience with Regulatory Documents/TMF

- support with study team meeting minutes

- strong organizational skills

- ability to multi-task

- possible experience with assisting with invoice processing/budgetary support (not oversight)