Clinical Data Assoc./Clin Data Mng-Atlanta, San Jose, San Deigo

Purpose of Position:
The primary focus of this position is on the management of Clinical Data Associates and the management of clinical trial data from the design of the case report form through the initiation of the final reporting process.

ASG, Inc. is a nationwide contract consulting and contingency recruiting firm. Our reputation for excellent service, our knowledge of the market place, and our success in the recruiting industry make it possible for us to provide complete and comprehensive contract consulting and contingency technical services. Align yourself with ASG and get: challenging assignments and competitive compensation (with or without benefits). Our job is to keep you focused on your work and to provide you with a comfortable working relationship with us, your business partner, ASG.
REQUIREMENTS
Skill Sets:
Oracle Clinical or Clintrial, SAS is nice but not preferred.
Education:
BS/BA degree required, with preference given to those in the scientific or analytical fields
Industry Experience Level:
2+ years of experience in a Pharmaceutical OR CRO environment

Requirements and Responsibilities:
•Responsible for management of Clinical Data Associates
•Provide training to Clinical Data Associates for study related activities
•Provide input to management team regarding Clinical Data Associate activities
•Act as Lead Clinical Data Associate for small to medium clinical trials (Phase I and II)
•Draft or supervise the creation of study startup documentation
•Attend study management team meetings (internal and with client)
•Act as primary contact for study team for data cleaning activities through database lock and freeze
•Assume direct responsibility for the final data quality
•Assist in the 1st and 2nd pass data entry of clinical data
•Regular client interaction, including limited travel
•Strict adherence to clients policies and procedures

This job is performed in a normal office environment. Physical requirements include ability to operate a personal computer, and to work at a desk for long periods of time with occasional opportunity to move to other locations within the building and surrounding locations for meetings, to obtain information, etc.

Education & Experience:
• BS/BA degree required, with preference given to those in the scientific or analytical fields
• Strong interpersonal and communication skills
• Ability to achieve results through innovation and initiative
• Strong problem solving skills
• Proven leadership and project management skills
• Thorough knowledge of medical and pharmaceutical industry, terminology, and practices
• Minimum 5 years direct data management experience with Phase III clinical trial data using a standard Clinical Trials database, experience with Oracle Clinical software preferred
• Demonstrated experience in the implementation of multiple studies conducted in several medical indications
• Knowledge of Adverse Event and Concomitant Medication data and the mapping to thesaurus terms helpful

If you would like to be considered for this position, please forward your resume to [Click here for email] please reference the job title and number.