Job Description
Job Description
Job Description
job summary:
- Utilizing extensive clinical data management experience in study start-up, conduct, and closeout you will oversee the data management deliverables across assigned therapeutic area (TA) programs or projects, and partner with cross functional study teams and FSP. You will focus on timely quality delivery, as well as consistency across the Global Study Operations Data Management (GSO-DM) components.
location: Telecommute
job type: Contract
salary: $65 - 75 per hour
work hours: 9 to 5
education: High School
responsibilities:
- Oversee GSO-DM Project Leads working on studies within a program to ensure delivery of all timelines and deliverables for the GSO-DM components on time and to a high standard of quality
- Plan and lead all aspects of GSO-DM activities for various TA programs, projects
- Risk, Resource, Strategic Portfolio, Quality and Stakeholder Management
- Act as a subject matter to ensure best practices in all GSO-DM processes and to ensure consistency within and across programs
- Identify process improvement opportunities and drive forward
- Evaluate the resourcing levels in partnership with FSP to ensure appropriate distribution and accountability for delivery of the portfolio demands.
- Contribute to the process and/or technical implementation of GSO-DM strategies
- Participate in cross functional key projects and/or working groups
- Develop, review, and implement policies, SOPs and associated documents affecting DM globally
- Provide technical and business process input / expertise and leadership on process improvement activities, new and emerging technologies
qualifications:
- Education & Experience: Ph.D. with 2+ years, M.S. with 6+ years, B.S. with 8+ years, A.S. with 10+ years, or High School/GED with 12+ years of experience.
- Leadership: Minimum 2 years of direct people management or leadership experience (teams, projects, etc.), which can overlap with the technical experience.
- Expertise: Extensive clinical data management experience in biotech/pharma, with a focus on study start-up, maintenance, and closeout. Direct oversight experience is required.
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skills: Clinical Data Management
Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.
At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact HRsupport@randstadusa.com.
Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including: medical, prescription, dental, vision, AD&D, and life insurance offerings, short-term disability, and a 401K plan (all benefits are based on eligibility).
This posting is open for thirty (30) days.
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Qualified applicants in San Francisco with criminal histories will be considered for employment in accordance with the San Francisco Fair Chance Ordinance.
Qualified applicants in the unincorporated areas of Los Angeles County with criminal histories will be considered for employment in accordance with the Los Angeles County's Fair Chance Ordinance for Employers.
We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance.
Job Tags
Hourly pay, Contract work, Temporary work, Work experience placement, Local area, Remote work,