Clinical Data Analyst (Thousand Oaks)

Job type:
on-site
Start:
05/2013
Duration:
12 Months
From:
Real Staffing
Place:
Thousand Oaks
Date:
05/05/2013
Country:
flag_no USA
project ID:
531960

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This project is archived and not active any more.
You will find vacant projects in our project database.
Job Requirements:

-Excellent analytical, problem-solving, organizational, time-management, interpersonal and communication skills

-In depth knowledge of all aspects of the clinical trials process from pre-clinical to post-marketing phases

-Ability to interpret and apply regulatory requirements

-Knowledgeable concerning all aspects of qualification and compliance assessments

-Demonstrated ability to effectively develop and manage relationships with ESPs

-Technical understanding of clinical research technologies and data validation methodologies

-Knowledge of systems integration and data interchange standards

-Proficient in the use of one or more of the leading Clinical Database Management Systems

-Experience supporting continuous process improvement initiatives with a proven track record of success as measured by return on investment

-Current with industry developments, trends and opportunities

Education and/or Experience:

-Minimum: BA/BS + 4 years experience or equivalent.

-Preferred: Master's degree in a related field. 3+ years of CDM experience in the Pharmaceutical, Device or Biotech industries (Sponsor, CRO or combination) in roles of increasing responsibility.

This is an excellent opportunity to become apart of an excellent organization within the Biotech industry. Please submit your resume to be considered for an interview.

To find out more about Real please visit www.realstaffing.com