Clinical Data Analyst (Thousand Oaks)

Thousand Oaks  ‐ Onsite
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Keywords

Description

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
Start date
05/2013
Duration
12 Months
From
Real Staffing
Published at
09.05.2013
Project ID:
533866
Contract type
Freelance
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