CDM System Administrator - (Gaithersburg, MD) - Gaithersburg, MD | Biospace
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CDM System Administrator - (Gaithersburg, MD)

MedImmune, LLC

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Location:
Gaithersburg, MD
Posted Date:
8/18/2017
Position Type:
Full time
Job Code:
R-006640
Salary:
Required Education:
Bachelors Degree
Areas of Expertise Desired:

Job Description

Location:
Gaithersburg, Maryland, United States
Job reference: R-006640
Posted date: May. 09, 2017

MedImmune is the worldwide biologics research and development arm of AstraZeneca. Here, you’ll have the opportunity to make a difference in people’s lives every day. As one of the world’s premier biotechnology companies, our mission is centered on delivering life-changing products that advance world health, and help fight and cure disease.  As a CDM System Administrator in Gaithersburg, MD, you’ll play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients’ lives.

We’re constantly pushing the boundaries of science to deliver life-changing medicines to patients, with a passion for discovery and a pipeline to show for it. We’re pioneering innovative research and exploring novel pathways across key therapeutic areas including oncology, respiratory, inflammation and autoimmunity, cardiovascular and metabolic disease, and infection and vaccines. And we’re industry-leading in immunology, protein engineering and translational science. We offer a unique and strong collaborative network as part of the AstraZeneca family, as together we explore synergies between small and large molecules.

MedImmune has a dynamic environment that fosters collaboration and innovation. We attract top minds, and we nurture and build top talent.

Main Duties and Responsibilities

As the CDM System Administrator, you will manage user access to clinical applications utilized by Clinical Data Management group.  Develop and maintain user access management documents and liaison between IT, Network Administrators, and Application Owners to maintain compliance.  You will function as an EDC SME for providing guidance and best practices to DM, Clinical teams and other stakeholders.

As the CDM System Administrator, you will be a SME for EDC between Data Management, CRO partners, and business stakeholders responsible to address escalation of study specific functional issues, tool issues, testing needs, enhancement requests, custom functions and/or custom reports.  Also, you will contribute/support integration of different clinical systems and similar initiatives that enhance efficiencies and quality of data management processes.  You will provide EDC technical support to facilitate clinical study timelines and deliverables.  Oversee the EDC Administrator role to support operational deliverables under Study Set Up, Study Maintenance, Study Conduct and Study Close Out.

Lastly, you will support technical systems access requests for all users including that may include outsourced trials, CROs and off-shore partners’ resources.

Requirements

Essential Requirements

  • BA / BS Computer Science/Information Technology or Life Sciences from a 4 year accredited university or equivalent experience.
  • Clinical programming experience is required.
  • Proficient computer skills across multiple applications.
  • Minimum 8 years clinical database programming experience preferred in the device / pharmaceutical / CRO industry.
  • Minimum 4 years database programming experience designing studies and data validation programming in EDC required; RAVE/Medidata Solutions preferred.

Desirable Requirements

  • Expert level experience with System administration activities involving Medidata suites of applications, SharePoint, IssueTrack and other industry standard CDM systems.
  • Proficient understanding of system administration to effectively interact with the tools and/or database administrators

Next Steps – Apply today!

To be considered for this exciting opportunity, please complete the full application on our website at your earliest convenience – it is the only way that our Recruiter and Hiring Manager can know that you feel well qualified for this opportunity.  If you know someone who would be a great fit, please share this posting with them.

AstraZeneca is an equal opportunity employer. AstraZeneca will consider all qualified applicants for employment without discrimination on grounds of disability, sex or sexual orientation, pregnancy or maternity leave status, race or national or ethnic origin, age, religion or belief, gender identity or re-assignment, marital or civil partnership status, protected veteran status (if applicable) or any other characteristic protected by law. AstraZeneca only employs individuals with the right to work in the country/ies where the role is advertised.

~bsp

*LI-MEDI