Specimen Processor - Pioneer Data Systems
New Haven, CT 06511
About the Job
Position Details:
Our client, a world-leading Pharmaceutical Company in New Haven, CT is currently looking for a Specimen Processor to join their expanding team.
Job Title: Specimen Processor
Duration: 17 months contract, extendable up to 36 months
Location: New Haven, CT
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Specimen Processor
Responsibilities:
Ensuring that samples acquired during the conduct of a drug trial are processed, stored, shipped in a manner that maintains specimen integrity
Review of queried reports to QC sample processing and bring to the attention of Operations Director any major protocol deviations and or discrepancies
Support sample processing and verification of specimen compliance
Identify day to day requirements for study sample processing and ensure that Laboratory is prepared to support these tasks
Maintain proper inventory of items necessary to support the processing and storage of clinical trial samples
Oversee the requisitioning and transport of safety samples that are outsourced
Perform the duties and requirements of Laboratory Study Co-lead
Record daily schedule for the following day by printing Dashboard schedule, 2 copies, deliver to SPL and Safety Lab
Display brief summary of next day's activities (including date) on the white board by the dumbwaiter
Ensure that samples acquired during the conduct of a drug trial are processed, stored, shipped in a manner that maintains specimen integrity
Once or twice a day, review of queried reports (Toad) to QC sample processing and bring to the attention of the Laboratory Manager or Specimen Processing Lead any major protocol deviations and or discrepancies who will then review issues with the lab
Document discrepancies on the electronic copy and save to the TAT folder, also include investigation comments in an additional column
Review daily Specimen Processing bench logs for compliance
Identify day-to-day requirements for study sample processing and ensure that Laboratory is prepared to support these tasks with trained personnel
Maintain inventory of items necessary to support the processing and storage of clinical trial samples
Enter send-out results as performed
Exhibit behavior by example, staying busy, ensuring the lab is covered at all times and new staff is not left alone
Qualifications:
High school diploma required, Associate's degree preferred
Minimum 0-3+ years of experience in a related field
Cerner Lab experience preferred
Hours:
Some flexibility is required/ weekend rotation is required
Shift: 6:30 AM - 3:00 PM
Our client, a world-leading Pharmaceutical Company in New Haven, CT is currently looking for a Specimen Processor to join their expanding team.
Job Title: Specimen Processor
Duration: 17 months contract, extendable up to 36 months
Location: New Haven, CT
Note:
The client has the right-to-hire you as a permanent employee at any time during or after the end of the contract.
You may participate in the company group medical insurance plan
Job Description:
Specimen Processor
Responsibilities:
Ensuring that samples acquired during the conduct of a drug trial are processed, stored, shipped in a manner that maintains specimen integrity
Review of queried reports to QC sample processing and bring to the attention of Operations Director any major protocol deviations and or discrepancies
Support sample processing and verification of specimen compliance
Identify day to day requirements for study sample processing and ensure that Laboratory is prepared to support these tasks
Maintain proper inventory of items necessary to support the processing and storage of clinical trial samples
Oversee the requisitioning and transport of safety samples that are outsourced
Perform the duties and requirements of Laboratory Study Co-lead
Record daily schedule for the following day by printing Dashboard schedule, 2 copies, deliver to SPL and Safety Lab
Display brief summary of next day's activities (including date) on the white board by the dumbwaiter
Ensure that samples acquired during the conduct of a drug trial are processed, stored, shipped in a manner that maintains specimen integrity
Once or twice a day, review of queried reports (Toad) to QC sample processing and bring to the attention of the Laboratory Manager or Specimen Processing Lead any major protocol deviations and or discrepancies who will then review issues with the lab
Document discrepancies on the electronic copy and save to the TAT folder, also include investigation comments in an additional column
Review daily Specimen Processing bench logs for compliance
Identify day-to-day requirements for study sample processing and ensure that Laboratory is prepared to support these tasks with trained personnel
Maintain inventory of items necessary to support the processing and storage of clinical trial samples
Enter send-out results as performed
Exhibit behavior by example, staying busy, ensuring the lab is covered at all times and new staff is not left alone
Qualifications:
High school diploma required, Associate's degree preferred
Minimum 0-3+ years of experience in a related field
Cerner Lab experience preferred
Hours:
Some flexibility is required/ weekend rotation is required
Shift: 6:30 AM - 3:00 PM
Source : Pioneer Data Systems