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Associate Director, Clinical Data Management - Fort Lauderdale, United States - Actalent
Description
:Develop and maintain study-specific documentation, including Data Management Plans, eCRF specifications, CRF Completion Guidelines, Data Validation Guidelines, add Data Transfer Specifications, Coding Guidelines, Post Production Database Change Control Documentation, Database Audit and Lock Procedures
EDC, uat testing, uat, CRO, vendor management, crf
Additional Skills & Qualifications:
ideally looking for a high-level Senior person coming from a CRO
this person would have 2-5 direct reports
Must haves:
CRO experience
Bachelor's degree
10 years of hands on DM experience, 2 years of management experience
60% hands on DM, 40% oversight
Ability to build an eCRF from scratch
UAT experience with or w/o scripts
Experience Level:
Expert Level
About Actalent
Actalent is a global leader in engineering and sciences services and talent solutions.
We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market.
With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.
Diversity, Equity & InclusionAt Actalent, diversity and inclusion are a bridge towards the equity and success of our people.
DE&I are embedded into our culture through:
The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.