Data Management Quality Associate (Oracle Clinical)
Streffco Consultants, Inc., is an international staffing and systems integration organization. We provide technology and business operations resources on a project, contract, contract-to-hire or direct hire basis.
Title: Data Management Quality Associate
Job ID: 6740
Industry: Biotech/Pharmaceutical
Location: Cambridge, MA
Duration: 7 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
Key
Responsibilities:
Review study documentation ensuring data quality is consistent with DM best practices, standards and procedures
Perform Trial Master File QC, document findings and remediate as applicable
Communicate lessons learned and recommend process improvements
Conduct parallel review and QC of DM deliverables from internal and vendor staff
Ensure DM activities are completed by vendors according to specified quality standards
Participate in inspection readiness tasks
Required Skills:
Strong understanding of end to end Clinical Data Management in a biotech or pharma environment (minimum
Experience: 5 years)
Experience working with DM vendors and CROs highly desirable
Familiarity with Oracle Clinical and/or Rave preferred
Solid working knowledge of MS Outlook, MS Word, MS Excel, MS PowerPoint
Excellent oral and written communication skills
Ability to manage multiple (changing) priorities under tight timelines
Detail oriented, able to identify issues and consistently collaborate to solve problems in a timely manner
Educational Requirements:
Bachelor of Science degree
Please respond by submitting your resume in a Word Document.
(Please include the job title and id# in the subject line)
We will not respond to everyone personally - qualified candidates will be contacted for an interview.
Estimated Salary: $20 to $28 per hour based on qualifications.
Title: Data Management Quality Associate
Job ID: 6740
Industry: Biotech/Pharmaceutical
Location: Cambridge, MA
Duration: 7 Month Contract
Pay Rate Range: Depends on Experience (W-2 all inclusive rate)
Key
Responsibilities:
Review study documentation ensuring data quality is consistent with DM best practices, standards and procedures
Perform Trial Master File QC, document findings and remediate as applicable
Communicate lessons learned and recommend process improvements
Conduct parallel review and QC of DM deliverables from internal and vendor staff
Ensure DM activities are completed by vendors according to specified quality standards
Participate in inspection readiness tasks
Required Skills:
Strong understanding of end to end Clinical Data Management in a biotech or pharma environment (minimum
Experience: 5 years)
Experience working with DM vendors and CROs highly desirable
Familiarity with Oracle Clinical and/or Rave preferred
Solid working knowledge of MS Outlook, MS Word, MS Excel, MS PowerPoint
Excellent oral and written communication skills
Ability to manage multiple (changing) priorities under tight timelines
Detail oriented, able to identify issues and consistently collaborate to solve problems in a timely manner
Educational Requirements:
Bachelor of Science degree
Please respond by submitting your resume in a Word Document.
(Please include the job title and id# in the subject line)
We will not respond to everyone personally - qualified candidates will be contacted for an interview.
Estimated Salary: $20 to $28 per hour based on qualifications.
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