Senior Clinical Research Associate

Employment Type: Full Time

The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.


Experience:
Strong computer and internet skills including knowledge of MS Office products such as Excel, Word


Strong regulatory knowledge including GCP


Excellent interpersonal, verbal and written communication skills


Sound problem solving skills


Looks for win-win solutions to solve problems


Gives others appropriate latitude to make decisions


Carefully weighs the priority of project tasks and directs team accordingly


Understands the strengths and development areas of team members


Enlists the support of team members in meetings goals


Ability to successfully work in a team environment


Ability to lead a virtual, global team as required


Sound presentation skills


Consultative skills


Ability to make appropriate decisions in ambiguous situations


Ability to solve problems by using a logical, systematic, sequential approach


Client focused approach to work with the ability to interact professionally within a client organization


Ability to prioritize multiple tasks and achieve project timelines


Effective time management in order to meet daily metrics or team objectives


Shows commitment to and performs consistently high quality work


Able to take initiative and work independently


Sense of urgency in completing assigned tasks


Able to travel up to 65% on average




Education


Educated to degree level (biological science, pharmacy or other health-related discipline preferred), equivalent nursing qualification or other equivalent experience

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