Remote Clinical Systems Manager Position Available In Durham, North Carolina
Tallo's Job Summary: The Remote Clinical Systems Manager position offers a 6-month contract with a pay rate of $64/hour W2, potentially extending or converting to permanent. Ideal candidates should have 10+ years of experience in Laboratory systems, including LIMS/Laboratory Management Electronic Smart Lab. Key skills include building master data, troubleshooting technical issues, and running queries for reporting data. Requirements include a Bachelor's Degree, strong problem-solving skills, and previous Pharma experience.
Job Description
REMOTE POSITION
;
CANDIDATES MUST BE WILLING TO TRAVEL AS NEEDED 6
Month Contract (May extend or convert to permanent) $64/hour W2
Ideal Candidate:
Ideally the candidate will have strong technical knowledge required to support deployment and support of Laboratory systems (LIMS/Laboratory Management Electronic Smart Lab). The candidate must have at least 10 years of functional experience and capable of leading Laboratory systems implementations, qualifications, and master data builds.
Top Must Have Skill Sets:
Experience with building masterdata for QC Laboratory Systems. Experience with troubleshooting technical issues. Experience with running queries for reporting data. Experience with Sample Manager
LIMS, CIMS, LMES
SmartLab Responsibilities:
Provide validation and qualification support for Laboratory systems deployment. Manage system masterdata builds and eProcedure Qualification support. Provide technical guidance for templating efficiencies within LIMS. Provide incident management support as required. Support Laboratory application performance monitoring and label printing issues. Identify technical/operational gaps and propose solutions. Provide hypercare support as systems go-live. Run LIMS queries as necessary, based on business needs. Ability to execute QC computer system validation and support/administer the system(s) when live in the production environment. Develops, writes, edits, and formats materials such as Standard Operating Procedures, Business Practices, forms, technical manuals, installation guides, user manuals, and related technical and business process documentation. Additionally, this position will be required to administer the processing of documents via the established Document Processing Review process. May require communication through a variety of media (e.g., intranet, on-line training, etc.)
Requirements:
Bachelor’s Degree or higher 10+ years of related experience, strong problem-solving skills, and previous Pharma experience preferred MS Office expertise Previous technical writing experience Regulated environment experience Document version control experience Excellent communication/writing skills
