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Senior Clinical Data Coordinator
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Senior Clinical Data Coordinator : MedImmune, LLC.
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| Job Number |
02171 |
| Employee Type |
Full Time |
| Company Name |
MedImmune, LLC. |
| Location |
Mountain View
California
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| Salary (year) |
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| Start Date |
1/18/2010 |
| Industry |
Biotech |
| Job Type |
Research-Translational-Science |
| Relocation |
Not Required |
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MedImmune, LLC.
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| What Does Your Boss Say About You? |
| Description |
Description
Title: Senior Clinical Data Coordinator
Location: CA, Mountain View - NON SALES
Req: 02171
Major Duties and Responsibilities (including supervising others):
• Support Studies as assigned
• Comply with all SOPs, regulatory guidelines, directives and study specific plans pertaining to the collection and review of lab data.
• Completes all assigned duties including, but not limited to:
• Support all data management functions as needed.
• Manage special projects as needed
• Represent function or department at MedImmune meetings
• Special projects for department
• Train other associates
• Perform change requests to existing study databases
• Write functional and cross-functional SOPs
About the Organization
My company shares my
passion for helping to improve human health around the world."
"This is My MedImmune."
Those who join MedImmune feel a sense of ownership about their future. They thrive with a recognized leader in the biotechnology industry and the wholly-owned subsidiary of AstraZeneca plc.
Here, you will join passionate professionals who advance science, technology and medicine to develop products designed to help people live better lives. You will excel in an environment characterized by respect, integrity and growth opportunities…that encourages both individual contribution and collaborative entrepreneurial thinking. Our products and/or product candidates are designed to address areas of need in infection, oncology, respiratory disease and inflammation, cardiovascular/gastrointestinal disease and neuroscience. Explore a MedImmune career as we strive to better more lives, more often, around the world.
Company Information
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| Requirements |
Position Requirements
• Minimum of 1-7 years in a related setting (clinical, data management, or laboratory). Experience with relational databases, knowledge of the Clinical Trials process and GxP, knowledge of Medical Terminology. Ability to query database for reporting purposes.
• Prior Sample Data management experience preferred.
• Experience with Microsoft based applications
• Previous Experience with Lab Ware LIMS preferred
Special Skills/Abilities:
• Excellent interpersonal, oral and written communication skills, including presentation skills.
• Strong ability to communicate clearly and concisely.
• Builds positive collaborative relationships with a variety of internal MedImmune staff and outside contacts.
• Ability to independently prioritize workload with a sense of urgency in completing work assignments
• Proven ability to move projects to completion
• Proven, sustained record of high-quality independent work
• Proven ability to identify, manage and mitigate risk
• Ability to define problems, collect data, establish facts, and draw valid conclusions
Job Complexity:
Works under limited supervision. Generally excercises independent discresion in determining plan for executing work. Work is only reviewed for soundness of technical judgment and accuracy on occasional basis.
Educational Requirements
Bachelors or Masters: Biotechnology; Life Sciences; Computer Sciences or related fields
MedImmune does not accept non-solicited resumes or candidate submittals from search/recruiting agencies not already on MedImmune’s approved agency list. Unsolicited resumes or candidate information submitted to MedImmune by search/recruiting agencies not already on MedImmune’s approved agency list shall become the property of MedImmune and if the candidate is subsequently hired by MedImmune, MedImmune shall not owe any fee to the submitting agency.
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